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      <title>Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</title>
      <link>https://onlinelibrary.wiley.com/journal/20426984?af=R</link>
      <description>Table of Contents for International Forum of Allergy &amp; Rhinology. List of articles from both the latest and EarlyView issues.</description>
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      <pubDate>Sun, 14 Jun 2026 07:50:12 +0000</pubDate>
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      <dc:title>Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</dc:title>
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         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70203?af=R</link>
         <pubDate>Sat, 13 Jun 2026 20:35:14 -0700</pubDate>
         <dc:date>2026-06-13T08:35:14-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
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         <title>Nationwide Real‐World Prescribing Patterns of Biologics in Chronic Rhinosinusitis With Nasal Polyps and Asthma</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Sun A Han, 
Dae Woo Kim, 
Seok‐Won Park, 
Jin Youp Kim
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Nationwide Real‐World Prescribing Patterns of Biologics in Chronic Rhinosinusitis With Nasal Polyps and Asthma</dc:title>
         <dc:identifier>10.1002/alr.70203</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70203</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70203?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70200?af=R</link>
         <pubDate>Fri, 12 Jun 2026 01:58:52 -0700</pubDate>
         <dc:date>2026-06-12T01:58:52-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
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         <guid isPermaLink="false">10.1002/alr.70200</guid>
         <title>Complications and Clinical Outcomes Following Modified Endoscopic Denker's With Pyriform Aperture Preservation: A Prospective Analysis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
The modified endoscopic Denker's (MED) approach provides access to all maxillary sinus (MS) walls for resection of various MS and retromaxillary pathologies, but the anteromedial maxilla has historically been resected. This study determined complication rates and outcomes following MED with pyriform aperture (PA) preservation (MEDPAP).


Methods
A prospective study was conducted on all adults who underwent MEDPAP for different MS or retromaxillary pathologies over 7.5 years. The following complications were collected at all postoperative visits: epiphora, hypesthesia or complete numbness (teeth, upper lip, lateral nasal sidewall, and cheek), crusting, nasal valve collapse (NVC), and empty nose syndrome 6‐item questionnaire (ENS6Q). Complications and disease recurrence rates were determined at a minimum 1 year for most complications and outcomes and 2 years for hypesthesia if hypesthesia had not resolved.


Results
Of 52 MEDPAP patients, median age was 58.5 years; 55.8% were male. Of 34.6% who experienced epiphora postoperatively, 7.7% persisted. When epiphora resolved, it did so by median 63.0 days. Sites of initial postoperative hypesthesia or numbness included teeth (23%–50%), upper lip (42%), nasal (22%), and cheek (30%). Hypesthesia resolved in 88%–100% of subsites by median 89.5–167.0 days. Hypesthesia persisted in 12% of patients (mainly anterior teeth). Crusting resolved in 97.8% by median 91.0 days. No patients developed NVC, and median final ENS6Q = 0.5 (range = 0–8). Non‐tumor disease and tumor recurrence rates were 0%.


Conclusions
MEDPAP was 100% successful at managing benign and select malignant MS pathologies during the study period. MEDPAP patients frequently experienced temporary epiphora and dentofacial hypesthesia or numbness that resolved by 2–6 months postoperatively. Epiphora and hypesthesia or numbness persisted in 7.7% and 12% of patients, respectively. No patients developed NVC or ENS.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The modified endoscopic Denker's (MED) approach provides access to all maxillary sinus (MS) walls for resection of various MS and retromaxillary pathologies, but the anteromedial maxilla has historically been resected. This study determined complication rates and outcomes following MED with pyriform aperture (PA) preservation (MEDPAP).&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A prospective study was conducted on all adults who underwent MEDPAP for different MS or retromaxillary pathologies over 7.5 years. The following complications were collected at all postoperative visits: epiphora, hypesthesia or complete numbness (teeth, upper lip, lateral nasal sidewall, and cheek), crusting, nasal valve collapse (NVC), and empty nose syndrome 6-item questionnaire (ENS6Q). Complications and disease recurrence rates were determined at a minimum 1 year for most complications and outcomes and 2 years for hypesthesia if hypesthesia had not resolved.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Of 52 MEDPAP patients, median age was 58.5 years; 55.8% were male. Of 34.6% who experienced epiphora postoperatively, 7.7% persisted. When epiphora resolved, it did so by median 63.0 days. Sites of initial postoperative hypesthesia or numbness included teeth (23%–50%), upper lip (42%), nasal (22%), and cheek (30%). Hypesthesia resolved in 88%–100% of subsites by median 89.5–167.0 days. Hypesthesia persisted in 12% of patients (mainly anterior teeth). Crusting resolved in 97.8% by median 91.0 days. No patients developed NVC, and median final ENS6Q = 0.5 (range = 0–8). Non-tumor disease and tumor recurrence rates were 0%.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;MEDPAP was 100% successful at managing benign and select malignant MS pathologies during the study period. MEDPAP patients frequently experienced temporary epiphora and dentofacial hypesthesia or numbness that resolved by 2–6 months postoperatively. Epiphora and hypesthesia or numbness persisted in 7.7% and 12% of patients, respectively. No patients developed NVC or ENS.&lt;/p&gt;</content:encoded>
         <dc:creator>
Yasser Almansour, 
Lane Donaldson, 
Khaled Kashlan, 
Swapna Vemuri, 
Jun Jin, 
John R. Craig
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Complications and Clinical Outcomes Following Modified Endoscopic Denker's With Pyriform Aperture Preservation: A Prospective Analysis</dc:title>
         <dc:identifier>10.1002/alr.70200</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70200</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70200?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70201?af=R</link>
         <pubDate>Tue, 09 Jun 2026 08:05:58 -0700</pubDate>
         <dc:date>2026-06-09T08:05:58-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70201</guid>
         <title>Evaluating the Potential Infectious Risk Profile of Biologics in Chronic Rhinosinusitis With Nasal Polyposis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Maxime Fieux, 
Philippe Gevaert, 
Leigh J. Sowerby
</dc:creator>
         <category>CLINICAL LETTER</category>
         <dc:title>Evaluating the Potential Infectious Risk Profile of Biologics in Chronic Rhinosinusitis With Nasal Polyposis</dc:title>
         <dc:identifier>10.1002/alr.70201</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70201</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70201?af=R</prism:url>
         <prism:section>CLINICAL LETTER</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70194?af=R</link>
         <pubDate>Tue, 09 Jun 2026 08:04:25 -0700</pubDate>
         <dc:date>2026-06-09T08:04:25-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70194</guid>
         <title>Translation and Cross‐Cultural Adaptation of the Chronic Rhinosinusitis Control Test for Global Use</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
The Chronic Rhinosinusitis Control Test (CRCT) is a patient‐reported outcome measure (PROM) written in English that is psychometrically validated to measure chronic rhinosinusitis control. Because the availability of translated PROMs is a driver of data equity—collection of data that is fair and generally representative—our objective was to create a library of translated, cross‐culturally adapted versions of the CRCT that could ultimately be used for patients worldwide.


Methods
A hybrid approach leveraging generative artificial intelligence (genAI) in collaboration with expert human linguists was employed for translation and cross‐cultural adaptation of the CRCT. For each target language, forward translations were performed with three large language models (LLMs) (ChatGPT, Copilot, and Perplexity) after which an expert human linguist provided additional revisions that were used to create a consensus final translation. Backward translations were performed using LLMs (Claude, Copilot, and Perplexity). The accuracy and validity of translations at each step were assessed qualitatively and quantitatively.


Results
The translation and cross‐cultural adaptation of the CRCT was achieved into 37 languages: Arabic, Bengali, Brazilian Portuguese, Bulgarian, Cantonese Chinese, Czech, Danish, Dutch, European Portuguese, Filipino, Finnish, French, German, Greek, Hebrew, Hindi, Hungarian, Indonesian, Italian, Japanese, Korean, Mandarin Chinese, Norwegian, Persian, Polish, Punjabi, Romanian, Russian, Serbo‐Croatian, Spanish, Swahili, Swedish, Thai, Turkish, Ukrainian, Urdu, and Vietnamese. These translated, cross‐culturally adapted versions of the CRCT are made available in this article.


Conclusion
Translated, cross‐culturally adapted versions of the CRCT developed in this study promote data equity by serving as a basis for psychometric validation of the CRCT for worldwide use.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;The Chronic Rhinosinusitis Control Test (CRCT) is a patient-reported outcome measure (PROM) written in English that is psychometrically validated to measure chronic rhinosinusitis control. Because the availability of translated PROMs is a driver of data equity—collection of data that is fair and generally representative—our objective was to create a library of translated, cross-culturally adapted versions of the CRCT that could ultimately be used for patients worldwide.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A hybrid approach leveraging generative artificial intelligence (genAI) in collaboration with expert human linguists was employed for translation and cross-cultural adaptation of the CRCT. For each target language, forward translations were performed with three large language models (LLMs) (ChatGPT, Copilot, and Perplexity) after which an expert human linguist provided additional revisions that were used to create a consensus final translation. Backward translations were performed using LLMs (Claude, Copilot, and Perplexity). The accuracy and validity of translations at each step were assessed qualitatively and quantitatively.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;The translation and cross-cultural adaptation of the CRCT was achieved into 37 languages: Arabic, Bengali, Brazilian Portuguese, Bulgarian, Cantonese Chinese, Czech, Danish, Dutch, European Portuguese, Filipino, Finnish, French, German, Greek, Hebrew, Hindi, Hungarian, Indonesian, Italian, Japanese, Korean, Mandarin Chinese, Norwegian, Persian, Polish, Punjabi, Romanian, Russian, Serbo-Croatian, Spanish, Swahili, Swedish, Thai, Turkish, Ukrainian, Urdu, and Vietnamese. These translated, cross-culturally adapted versions of the CRCT are made available in this article.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Translated, cross-culturally adapted versions of the CRCT developed in this study promote data equity by serving as a basis for psychometric validation of the CRCT for worldwide use.&lt;/p&gt;</content:encoded>
         <dc:creator>
Hye K. Pae, 
Detong Xia, 
Hanzhong Sun, 
Yudi Chen, 
Kwangoh Yi, 
Minjeong Song, 
Eriko Sato, 
Ali R. Abasi, 
Jody Ballah, 
Anna Babarczy, 
Raymond Bertram, 
Agnieszka Biernacka, 
Mable Chan, 
Teresa Civera, 
Irina Dubinina, 
Doğu Erdener, 
María Isabel Maldonado García, 
Ali Garib, 
Tuomo Häikiö, 
Fuk‐chuen HO, 
Li‐Yu Hung, 
R. Malatesha Joshi, 
Oksana Kanerva, 
Kiranpreet Kaur Baath, 
Björn Köhnlein, 
Dalibor Kučera, 
Paula Luegi, 
Yustinus Calvin Gai Mali, 
Sivan Medina, 
Stefan Milosavljević, 
Amna Mirza, 
Mohamed Y. Mwamzandi, 
Fatemeh Nami, 
Anabella‐Gloria Niculescu‐Gorpin, 
Portia Padilla, 
Georgia Panayiotou, 
Manuel Perea, 
Luciano Perondi, 
Hiển Phạm, 
Rasmus Puggaard‐Rode, 
Anurag Rimzhim, 
Sreeparna Sarkar, 
David L. Share, 
Gláucia V. Silva, 
Antônio R. M. Simões, 
Charlotte Stormbom, 
Titima Suthiwan, 
Katsuo Tamaoka, 
Mila Tasseva‐Kurktchieva, 
Paweł Urbanik, 
An Van, 
Katie M. Phillips, 
Ahmad R. Sedaghat
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Translation and Cross‐Cultural Adaptation of the Chronic Rhinosinusitis Control Test for Global Use</dc:title>
         <dc:identifier>10.1002/alr.70194</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70194</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70194?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70202?af=R</link>
         <pubDate>Mon, 08 Jun 2026 05:45:43 -0700</pubDate>
         <dc:date>2026-06-08T05:45:43-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70202</guid>
         <title>Region‐Resolved Proteomics Identifies Molecular Features at the Mucosa‐Polyp Interface in Chronic Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Yi‐Sook Kim, 
Hong‐Beom Park, 
Roza Khalmuratova, 
Hyun Kyung Lee, 
Doo Hee Han, 
Dae Woo Kim, 
Dohyun Han, 
Hyun‐Woo Shin
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Region‐Resolved Proteomics Identifies Molecular Features at the Mucosa‐Polyp Interface in Chronic Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70202</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70202</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70202?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70145?af=R</link>
         <pubDate>Fri, 05 Jun 2026 23:58:30 -0700</pubDate>
         <dc:date>2026-06-05T11:58:30-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70145</guid>
         <title>Gaze Mapping and Observational Behavior During Nasal Endoscopy</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
William S. Smithee, 
Duncan G. J. Green, 
Quinn F. O'Malley, 
Arjun Yusufji, 
Jonathan M. Owens, 
Edward D. McCoul
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Gaze Mapping and Observational Behavior During Nasal Endoscopy</dc:title>
         <dc:identifier>10.1002/alr.70145</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70145</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70145?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70195?af=R</link>
         <pubDate>Fri, 05 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-05T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70195</guid>
         <title>Assessment of MUcociLiary Transport timE in CRSwNP Patients in Treatment With Dupilumab: AMULET Study</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Alessia Giorli, 
Fabio Ferretti, 
Antonio Romano, 
Marco Casiraghi, 
Mariella Scarano, 
Paolo Farneti, 
Giacomo Sollini, 
Marco Mandalà, 
Ernesto Pasquini, 
Cesare Biagini
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Assessment of MUcociLiary Transport timE in CRSwNP Patients in Treatment With Dupilumab: AMULET Study</dc:title>
         <dc:identifier>10.1002/alr.70195</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70195</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70195?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70198?af=R</link>
         <pubDate>Thu, 04 Jun 2026 01:59:48 -0700</pubDate>
         <dc:date>2026-06-04T01:59:48-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70198</guid>
         <title>Stratified Anti‐Biofilm Therapy: Translating Staphylococcal Exoprotein Toxicity Hierarchies Into Clinical Practice</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Peiling Li, 
Tingting Kang
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Stratified Anti‐Biofilm Therapy: Translating Staphylococcal Exoprotein Toxicity Hierarchies Into Clinical Practice</dc:title>
         <dc:identifier>10.1002/alr.70198</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70198</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70198?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70199?af=R</link>
         <pubDate>Thu, 04 Jun 2026 01:57:32 -0700</pubDate>
         <dc:date>2026-06-04T01:57:32-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70199</guid>
         <title>Reply to Stratified Anti‐Biofilm Therapy: Translating Staphylococcal Exoprotein Toxicity Hierarchies Into Clinical Practice</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Sarah Vreugde, 
Sintayehu Ambachew, 
Alkis James Psaltis, 
Peter‐John Wormald
</dc:creator>
         <category>REPLY</category>
         <dc:title>Reply to Stratified Anti‐Biofilm Therapy: Translating Staphylococcal Exoprotein Toxicity Hierarchies Into Clinical Practice</dc:title>
         <dc:identifier>10.1002/alr.70199</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70199</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70199?af=R</prism:url>
         <prism:section>REPLY</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70197?af=R</link>
         <pubDate>Wed, 03 Jun 2026 02:59:43 -0700</pubDate>
         <dc:date>2026-06-03T02:59:43-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70197</guid>
         <title>Potential Clinical Impact of Sinonasal Biofilms in CRS: A Structured Evidence Synthesis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Hunter A. Holley, 
Nitish Kumar, 
Diana Segovia, 
Devyani Lal, 
Amar Miglani, 
Michael J. Marino
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Potential Clinical Impact of Sinonasal Biofilms in CRS: A Structured Evidence Synthesis</dc:title>
         <dc:identifier>10.1002/alr.70197</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70197</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70197?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70185?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70185</guid>
         <title>Issue Information</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 537-539, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator/>
         <category>ISSUE INFORMATION</category>
         <dc:title>Issue Information</dc:title>
         <dc:identifier>10.1002/alr.70185</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70185</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70185?af=R</prism:url>
         <prism:section>ISSUE INFORMATION</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70172?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70172</guid>
         <title>Correction to “Dosing Interval Extension of Dupilumab in CRSwNP: Five‐Year Real World Outcomes”</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 654-655, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator/>
         <category>ERRATUM</category>
         <dc:title>Correction to “Dosing Interval Extension of Dupilumab in CRSwNP: Five‐Year Real World Outcomes”</dc:title>
         <dc:identifier>10.1002/alr.70172</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70172</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70172?af=R</prism:url>
         <prism:section>ERRATUM</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70173?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70173</guid>
         <title>Disease Remission: A Scoping Review With Thematic Analysis of the Scientific Literature With Implications for Chronic Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 615-629, June 2026. </description>
         <dc:description>
ABSTRACT

Background
Remission, a term used to describe a goal of treatment for some chronic diseases, has recently been proposed for chronic rhinosinusitis (CRS). However, it is unclear what remission means for CRS and why it should serve as a goal in the present‐day treatment of CRS.


Methods
Systematic literature search of PubMed, Embase, Scopus, and CINAHL databases for definitions of remission for chronic nonneoplastic diseases derived through consensus studies or society‐sponsored position papers. Remission definitions were extracted and common themes identified.


Results
Thirty‐nine definitions of remission were identified, the majority (29/39) of which were for inflammatory diseases. Remission uniformly was a term describing a state of completely inactive or minimally active disease, often defined by criteria including patient‐reported outcomes, clinician‐reported outcomes, and results from physical examination or serological, histologic, imaging findings, or other disease‐specific testing. Definitions varied in specifying different categories/levels of remission. However, most definitions stipulated a specific purpose for remission as providing a unique positive prognostic benefit to patients, commonly as cessation of end‐organ damage/disease progression. Diseases that also utilized control as an outcome differentiated remission as a state of lesser disease activity.


Conclusions
Commonalities from previously described remission definitions can be applied to define CRS remission as a state of minimal‐to‐no disease activity characterized by criteria reflecting the CRS disease process, the achievement of which would provide specific prognostic, future benefit to the patient. However, evidence is still lacking to support the utility or an exact definition of a remission construct for CRS.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Remission, a term used to describe a goal of treatment for some chronic diseases, has recently been proposed for chronic rhinosinusitis (CRS). However, it is unclear what remission means for CRS and why it should serve as a goal in the present-day treatment of CRS.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Systematic literature search of PubMed, Embase, Scopus, and CINAHL databases for definitions of remission for chronic nonneoplastic diseases derived through consensus studies or society-sponsored position papers. Remission definitions were extracted and common themes identified.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Thirty-nine definitions of remission were identified, the majority (29/39) of which were for inflammatory diseases. Remission uniformly was a term describing a state of completely inactive or minimally active disease, often defined by criteria including patient-reported outcomes, clinician-reported outcomes, and results from physical examination or serological, histologic, imaging findings, or other disease-specific testing. Definitions varied in specifying different categories/levels of remission. However, most definitions stipulated a specific purpose for remission as providing a unique positive prognostic benefit to patients, commonly as cessation of end-organ damage/disease progression. Diseases that also utilized control as an outcome differentiated remission as a state of lesser disease activity.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Commonalities from previously described remission definitions can be applied to define CRS remission as a state of minimal-to-no disease activity characterized by criteria reflecting the CRS disease process, the achievement of which would provide specific prognostic, future benefit to the patient. However, evidence is still lacking to support the utility or an exact definition of a remission construct for CRS.&lt;/p&gt;</content:encoded>
         <dc:creator>
Nikhil Parail, 
Lynn Warner, 
Stacey T. Gray, 
Claire Hopkins, 
Peter H. Hwang, 
Sarah K. Wise, 
Katie M. Phillips, 
Ahmad R. Sedaghat
</dc:creator>
         <category>REVIEW ARTICLE</category>
         <dc:title>Disease Remission: A Scoping Review With Thematic Analysis of the Scientific Literature With Implications for Chronic Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70173</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70173</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70173?af=R</prism:url>
         <prism:section>REVIEW ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70162?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70162</guid>
         <title>Evaluation of the Quality of Life in Adults With Acute Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 633-635, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Melissa Cummins, 
Ruifeng Cui, 
Ashley O'Malley, 
Hassan H. Ramadan, 
Chadi A. Makary
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Evaluation of the Quality of Life in Adults With Acute Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70162</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70162</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70162?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70164?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70164</guid>
         <title>Air Quality Index Association With Cytokine Inflammatory Markers in Chronic Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 630-632, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Nanda Nayak, 
Christina Dorismond, 
Rory Lubner, 
Daniel Lofgren, 
Ping Li, 
Katherine Cahill, 
Mason Krysinski, 
Rakesh Chandra, 
Justin Turner, 
Naweed Chowdhury
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Air Quality Index Association With Cytokine Inflammatory Markers in Chronic Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70164</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70164</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70164?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70175?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70175</guid>
         <title>Wearable Activity Data Demonstrate an Association Between Sinus Surgery and Improved Real‐World Activity</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 643-645, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Cole L. Bird, 
Rahul Alapati, 
Frank T. Materia, 
Angela Kaczorowski‐Worthley, 
Vidur Bhalla, 
D. David Beahm, 
Jamie R. Oliver
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Wearable Activity Data Demonstrate an Association Between Sinus Surgery and Improved Real‐World Activity</dc:title>
         <dc:identifier>10.1002/alr.70175</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70175</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70175?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70169?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70169</guid>
         <title>Exploring Sleep Quality and Chronic Rhinosinusitis Risk Using Wearable Technology</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 636-639, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Justina Varghese, 
Aakash Agarwal, 
Akshay R. Prabhakar, 
Heli Majeethia, 
Daniel Gorelik, 
Sebastian Guadarrama‐Sistos‐Vazquez, 
Renjie Hu, 
Michael T. Yim, 
Ron L. Moses, 
Masayoshi Takashima, 
Omar G. Ahmed
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Exploring Sleep Quality and Chronic Rhinosinusitis Risk Using Wearable Technology</dc:title>
         <dc:identifier>10.1002/alr.70169</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70169</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70169?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70177?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70177</guid>
         <title>Fascia‐Fat‐Fascia “Sandwich Graft” Decreases Postoperative Cerebrospinal Fluid Leak Rate for High‐Flow Skull Base Defects</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 646-649, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Vidit M. Talati, 
Kathy Zhang, 
Kimberly X. Wei, 
Margaret B. Mitchell, 
Nithin D. Adappa, 
Michael A. Kohanski, 
Jennifer E. Douglas, 
Christina Jackson, 
John Y. K. Lee, 
Phillip B. Storm, 
Jillian W. Lazor, 
James N. Palmer
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Fascia‐Fat‐Fascia “Sandwich Graft” Decreases Postoperative Cerebrospinal Fluid Leak Rate for High‐Flow Skull Base Defects</dc:title>
         <dc:identifier>10.1002/alr.70177</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70177</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70177?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70180?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70180</guid>
         <title>Deep Learning‐Based Cribriform Segmentation and Automated Olfactory Fossa Depth Estimation on Sinus CT</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 650-653, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Jamie Oliver, 
Ann Weesner, 
Ryan Henn, 
Sterling Anderson, 
Alexandria Yao, 
Easton Attwood, 
Rahul Alapati, 
Vidur Bhalla, 
David Beahm, 
Jennifer Villwock, 
Andrés Bur
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Deep Learning‐Based Cribriform Segmentation and Automated Olfactory Fossa Depth Estimation on Sinus CT</dc:title>
         <dc:identifier>10.1002/alr.70180</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70180</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70180?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70174?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70174</guid>
         <title>Effect of Platelet‐Rich Plasma and Hyaluronic Acid Olfactory Cleft Injection on Traumatic Olfactory Dysfunction: A Prospective Randomized Clinical Trial</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 640-642, June 2026. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Rong‐San Jiang, 
Jing‐Jie Wang
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Effect of Platelet‐Rich Plasma and Hyaluronic Acid Olfactory Cleft Injection on Traumatic Olfactory Dysfunction: A Prospective Randomized Clinical Trial</dc:title>
         <dc:identifier>10.1002/alr.70174</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70174</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70174?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70101?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70101</guid>
         <title>Impedance‐Controlled Multipoint Radiofrequency Ablation for Chronic Rhinitis: A Randomized Controlled Trial</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 553-560, June 2026. </description>
         <dc:description>
ABSTRACT

Background
The purpose of this randomized controlled trial (RCT) was to demonstrate that posterior nasal nerve ablation treatment with the NEUROMARK System is superior to a sham control procedure in patients with chronic rhinitis.


Methods
In this prospective, multicenter, single‐blinded, superiority RCT, 132 participants were randomized 2:1 to the active treatment arm (88) and sham control arm (44). The primary endpoint was the comparison of the reflective Total Nasal Symptom Score (rTNSS) responder rate between study arms at 90‐day follow‐up. Secondary efficacy outcomes included postnasal drip, chronic cough, Nasal Obstruction Symptom Evaluation (NOSE), mini‐Rhinoconjunctivitis Quality of Life Questionnaire (mini‐RQLQ), and Patient Health Questionnaire‐9 (PHQ‐9) (a depression assessment).


Results
The responder rate was significantly higher for the active treatment arm: 73.3% (95% confidence interval [CI], 64.0%–82.7%) compared to the sham control arm: 35.0% (95% CI, 20.2%–49.8%; p &lt; 0.001). The primary endpoint was met, demonstrating the active treatment arm is superior to the sham control arm. The active treatment arm had significantly greater decreases (improvements) in the rTNSS (–4.0 vs. –1.2, p &lt; 0.0001), postnasal drip (–1.1 vs. –0.3, p &lt; 0.001), cough (–0.9 vs. –0.1, p &lt; 0.001), NOSE score (–32.2 vs. –8.0, p &lt; 0.0001), mini‐RQLQ (–1.7 vs. –0.5, p &lt; 0.0001), and PHQ‐9 (–3.0 vs. –0.7, p = 0.028), compared to the sham control arm. The NOSE responder rate and mini‐RQLQ responder rate were significantly higher for the active treatment arm than the sham control arm (p = 0.001 and p &lt; 0.0001, respectively).


Conclusion
Treatment for chronic rhinitis with the NEUROMARK System is superior to sham control.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The purpose of this randomized controlled trial (RCT) was to demonstrate that posterior nasal nerve ablation treatment with the NEUROMARK System is superior to a sham control procedure in patients with chronic rhinitis.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;In this prospective, multicenter, single-blinded, superiority RCT, 132 participants were randomized 2:1 to the active treatment arm (88) and sham control arm (44). The primary endpoint was the comparison of the reflective Total Nasal Symptom Score (rTNSS) responder rate between study arms at 90-day follow-up. Secondary efficacy outcomes included postnasal drip, chronic cough, Nasal Obstruction Symptom Evaluation (NOSE), mini-Rhinoconjunctivitis Quality of Life Questionnaire (mini-RQLQ), and Patient Health Questionnaire-9 (PHQ-9) (a depression assessment).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;The responder rate was significantly higher for the active treatment arm: 73.3% (95% confidence interval [CI], 64.0%–82.7%) compared to the sham control arm: 35.0% (95% CI, 20.2%–49.8%; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001). The primary endpoint was met, demonstrating the active treatment arm is superior to the sham control arm. The active treatment arm had significantly greater decreases (improvements) in the rTNSS (–4.0 vs. –1.2, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001), postnasal drip (–1.1 vs. –0.3, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), cough (–0.9 vs. –0.1, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), NOSE score (–32.2 vs. –8.0, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001), mini-RQLQ (–1.7 vs. –0.5, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001), and PHQ-9 (–3.0 vs. –0.7, &lt;i&gt;p&lt;/i&gt; = 0.028), compared to the sham control arm. The NOSE responder rate and mini-RQLQ responder rate were significantly higher for the active treatment arm than the sham control arm (&lt;i&gt;p&lt;/i&gt; = 0.001 and &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001, respectively).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Treatment for chronic rhinitis with the NEUROMARK System is superior to sham control.&lt;/p&gt;</content:encoded>
         <dc:creator>
Masayoshi Takashima, 
Randall A. Ow, 
Richard D. Thrasher, 
Ellen M. O'Malley, 
William R. Blythe, 
Omar G. Ahmed
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Impedance‐Controlled Multipoint Radiofrequency Ablation for Chronic Rhinitis: A Randomized Controlled Trial</dc:title>
         <dc:identifier>10.1002/alr.70101</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70101</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70101?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70105?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70105</guid>
         <title>Appropriate Medical Therapy Primarily Modifies Type 2 and Severity Biomarkers in Chronic Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 595-606, June 2026. </description>
         <dc:description>
ABSTRACT

Background
Appropriate medical therapy (AMT) is first‐line treatment for patients with chronic rhinosinusitis (CRS). We evaluated inflammatory structure, treatment‐induced changes, and biomarker‐outcome associations in AMT‐managed patients.


Methods
Fifty‐one CRS patients were evaluated before and after AMT which included a combination of oral antibiotics, oral steroids, or intranasal steroids tailored to CRS phenotype and severity. At each visit, patients completed the SNOT‐22, CRS‐PRO, Brief Smell Identification Test (BSIT), CT scan (Lund–Mackay Score [LM]), and endoscopy (Modified Lund–Kennedy Score [MLK]). Middle‐meatal mucus was analyzed for IL‐1b, IL‐5, IL‐13, IFN‐g, and MIP1a using Luminex and ELISA. Principal components analysis (PCA) was performed on baseline cytokine data to identify key biomarker axes. Paired‐sample Wilcoxon tests compared cytokine changes, and Spearman's correlation assessed relationships between biomarkers and disease measures.


Results
PCA revealed two major components: PC‐1 (inflammation severity) dominated by ECP and MIP1a, and PC‐2 (endotype axis) with positive weighting of IL‐5 and IL‐13 (T2) and negative weighting of IFN‐g and IL‐1b (T1/3). AMT significantly reduced inflammatory severity and T2 biomarker burden, driven by decreases in IL‐5, IL‐13, ECP, and MIP1a (all p &lt; 0.01), while T1/3 biomarker remained unchanged. Clinical outcomes, including MLK, SNOT‐22, CRS‐PRO, and BSIT, improved and showed stronger correlations with T2 than T1/3 biomarkers.


Conclusion
AMT for CRS is associated with reduction in index biomarkers across inflammatory severity and T2 endotype with minimal effects on T1/3 inflammation. T2‐driven inflammation appears to be the most AMT‐responsive axis found in this study, aligning with measurable improvements in endoscopic, patient reported, and nasal airflow outcomes.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Appropriate medical therapy (AMT) is first-line treatment for patients with chronic rhinosinusitis (CRS). We evaluated inflammatory structure, treatment-induced changes, and biomarker-outcome associations in AMT-managed patients.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Fifty-one CRS patients were evaluated before and after AMT which included a combination of oral antibiotics, oral steroids, or intranasal steroids tailored to CRS phenotype and severity. At each visit, patients completed the SNOT-22, CRS-PRO, Brief Smell Identification Test (BSIT), CT scan (Lund–Mackay Score [LM]), and endoscopy (Modified Lund–Kennedy Score [MLK]). Middle-meatal mucus was analyzed for IL-1b, IL-5, IL-13, IFN-g, and MIP1a using Luminex and ELISA. Principal components analysis (PCA) was performed on baseline cytokine data to identify key biomarker axes. Paired-sample Wilcoxon tests compared cytokine changes, and Spearman's correlation assessed relationships between biomarkers and disease measures.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;PCA revealed two major components: PC-1 (inflammation severity) dominated by ECP and MIP1a, and PC-2 (endotype axis) with positive weighting of IL-5 and IL-13 (T2) and negative weighting of IFN-g and IL-1b (T1/3). AMT significantly reduced inflammatory severity and T2 biomarker burden, driven by decreases in IL-5, IL-13, ECP, and MIP1a (all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.01), while T1/3 biomarker remained unchanged. Clinical outcomes, including MLK, SNOT-22, CRS-PRO, and BSIT, improved and showed stronger correlations with T2 than T1/3 biomarkers.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;AMT for CRS is associated with reduction in index biomarkers across inflammatory severity and T2 endotype with minimal effects on T1/3 inflammation. T2-driven inflammation appears to be the most AMT-responsive axis found in this study, aligning with measurable improvements in endoscopic, patient reported, and nasal airflow outcomes.&lt;/p&gt;</content:encoded>
         <dc:creator>
Asher C. Park, 
Brooke N. Gleason, 
Eli Stein, 
Saied Ghadersohi, 
Atsushi Kato, 
Stephanie Shintani‐Smith, 
David B. Conley, 
Kevin C. Welch, 
Robert C. Kern, 
Bruce K. Tan
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Appropriate Medical Therapy Primarily Modifies Type 2 and Severity Biomarkers in Chronic Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70105</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70105</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70105?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70092?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70092</guid>
         <title>A Dual Setback: Staphylococcus aureus Biofilms From Severe Chronic Rhinosinusitis Show Enhanced Virulence Capacity and Tolerance to Antibiotics</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 541-552, June 2026. </description>
         <dc:description>
ABSTRACT

Background
Staphylococcus aureus biofilms play a crucial role in chronic rhinosinusitis (CRS), leading to the persistence of symptoms. Severe CRS patients are frequently infected with S. aureus strains that exhibit higher biofilm properties (e.g., biomass, exoprotein production) compared to S. aureus from controls. S. aureus biofilms resist antibiotic treatment; however, the relationship between bacterial biofilm properties, antibiotic susceptibility, and CRS severity has not yet been defined and is the subject of this study.


Methods
S. aureus clinical isolates and reference strains, and matched clinical datasets were collected from CRS patients and controls (n  =  35). Antimicrobial susceptibility of the isolates to clindamycin, mupirocin, clarithromycin, doxycycline, and amoxicillin‐clavulanic acid was determined by minimum inhibitory concentration (MIC) and minimum biofilm eradication concentration (MBEC).


Results
S. aureus MBEC values (n  =  35) were significantly higher (up to 11 times) than the MIC for all five antibiotics (p &lt; 0.001). Among the various antibiotics tested, mupirocin had the strongest antibiofilm activity and amoxicillin‐clavulanic acid the weakest: at antibiotic concentrations that are deemed to indicate susceptibility or intermediate resistance when testing in planktonic form, 80% biofilm eradication was reached for all isolates using mupirocin and only 5/35 isolates using amoxicillin‐clavulanic acid. The biofilm metabolic activity, biomass, colony‐forming units, and exoprotein production were positively correlated with the MBEC values for amoxicillin‐clavulanic acid and clarithromycin, but not for the other antibiotics. Lund–Mackay and Lund–Kennedy disease severity scores showed positive correlations with the MBEC values of clarithromycin.


Conclusion
These findings show that whilst severe CRS patients are frequently infected with S. aureus strains that exhibit higher biofilm‐mediated virulence, these biofilms are also more difficult to control with standard of care antibiotics. Better personalized therapies are required to manage biofilm‐mediated infections in severe CRS patients.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;&lt;i&gt;Staphylococcus aureus&lt;/i&gt; biofilms play a crucial role in chronic rhinosinusitis (CRS), leading to the persistence of symptoms. Severe CRS patients are frequently infected with &lt;i&gt;S. aureus&lt;/i&gt; strains that exhibit higher biofilm properties (e.g., biomass, exoprotein production) compared to &lt;i&gt;S. aureus&lt;/i&gt; from controls. &lt;i&gt;S. aureus&lt;/i&gt; biofilms resist antibiotic treatment; however, the relationship between bacterial biofilm properties, antibiotic susceptibility, and CRS severity has not yet been defined and is the subject of this study.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;&lt;i&gt;S. aureus&lt;/i&gt; clinical isolates and reference strains, and matched clinical datasets were collected from CRS patients and controls (&lt;i&gt;n&lt;/i&gt;  =  35). Antimicrobial susceptibility of the isolates to clindamycin, mupirocin, clarithromycin, doxycycline, and amoxicillin-clavulanic acid was determined by minimum inhibitory concentration (MIC) and minimum biofilm eradication concentration (MBEC).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;&lt;i&gt;S. aureus&lt;/i&gt; MBEC values (&lt;i&gt;n&lt;/i&gt;  =  35) were significantly higher (up to 11 times) than the MIC for all five antibiotics (&lt;i&gt;p &lt;/i&gt;&amp;lt; 0.001). Among the various antibiotics tested, mupirocin had the strongest antibiofilm activity and amoxicillin-clavulanic acid the weakest: at antibiotic concentrations that are deemed to indicate susceptibility or intermediate resistance when testing in planktonic form, 80% biofilm eradication was reached for all isolates using mupirocin and only 5/35 isolates using amoxicillin-clavulanic acid. The biofilm metabolic activity, biomass, colony-forming units, and exoprotein production were positively correlated with the MBEC values for amoxicillin-clavulanic acid and clarithromycin, but not for the other antibiotics. Lund–Mackay and Lund–Kennedy disease severity scores showed positive correlations with the MBEC values of clarithromycin.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;These findings show that whilst severe CRS patients are frequently infected with &lt;i&gt;S. aureus&lt;/i&gt; strains that exhibit higher biofilm-mediated virulence, these biofilms are also more difficult to control with standard of care antibiotics. Better personalized therapies are required to manage biofilm-mediated infections in severe CRS patients.&lt;/p&gt;</content:encoded>
         <dc:creator>
Gohar Shaghayegh, 
Clare Cooksley, 
Cate Cheney, 
Sima Kianpour Rad, 
Beula Subashini Panchatcharam, 
Emma F. Barry, 
Sholeh Feizi, 
George Bouras, 
Alkis James Psaltis, 
Peter‐John Wormald, 
Sarah Vreugde
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>A Dual Setback: Staphylococcus aureus Biofilms From Severe Chronic Rhinosinusitis Show Enhanced Virulence Capacity and Tolerance to Antibiotics</dc:title>
         <dc:identifier>10.1002/alr.70092</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70092</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70092?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70098?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70098</guid>
         <title>Local Specific IgE Levels Can Predict and Monitor the Therapeutic Response to Subcutaneous Immunotherapy With House Dust Mite</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 561-571, June 2026. </description>
         <dc:description>
ABSTRACT

Background
Identifying predictive and monitoring biomarkers for allergen immunotherapy response is crucial for enhancing clinical efficacy. This study aims to investigate the systemic and local levels of immunoglobulins and identify potential biomarkers in house dust mite (HDM) allergic rhinitis (AR) patients who are undergoing subcutaneous immunotherapy (SCIT).


Methods
This study enrolled 114 AR patients who completed 1‐year SCIT follow‐up. High responders and low responders were classified based on &gt;30% improvement in the average total combined score (ATCS). Immunoglobulin levels of HDM and its major components were measured in serum and nasal secretions before and after treatment. Predictive index (Pi) and therapeutic index (Ti) analyses were performed using linear regression to assess the impact of baseline immunoglobulin concentrations and their pre‐ to post‐treatment changes on symptom alleviation. Receiver operating characteristic (ROC) curve analysis with area under the curve (AUC) quantification was performed to evaluate predictive value for clinical responses.


Results
Positive SCIT response correlated with lower baseline age and higher symptom scores, allergen‐specific IgE (sIgE) levels, and sIgE/total IgE (tIgE) ratio. Pi analysis revealed that elevated pre‐treatment nasal sIgE levels and higher sIgE/tIgE ratios for Der p, Der f, Der p 1, and Der p 2 distinguished high from low responders. Ti analysis showed that post‐treatment decreases in these nasal sIgE levels correlated with improved clinical outcomes. Logistic regression showed baseline sIgE/tIgE ratios for Der p and Der f both in serum and nasal secretions, and Der p 1 and Der p 2 in serum positively correlated with clinical improvement. The sIgE/tIgE ratios of Der p (0.833 vs. 0.758) and Der f (0.813 vs. 0.738) in nasal secretions exhibited higher AUC values compared to serum.


Conclusions
Immunologic indicators in nasal secretions are potential biomarkers for the effective prediction and monitoring of early SCIT responses.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Identifying predictive and monitoring biomarkers for allergen immunotherapy response is crucial for enhancing clinical efficacy. This study aims to investigate the systemic and local levels of immunoglobulins and identify potential biomarkers in house dust mite (HDM) allergic rhinitis (AR) patients who are undergoing subcutaneous immunotherapy (SCIT).&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This study enrolled 114 AR patients who completed 1-year SCIT follow-up. High responders and low responders were classified based on &amp;gt;30% improvement in the average total combined score (ATCS). Immunoglobulin levels of HDM and its major components were measured in serum and nasal secretions before and after treatment. Predictive index (Pi) and therapeutic index (Ti) analyses were performed using linear regression to assess the impact of baseline immunoglobulin concentrations and their pre- to post-treatment changes on symptom alleviation. Receiver operating characteristic (ROC) curve analysis with area under the curve (AUC) quantification was performed to evaluate predictive value for clinical responses.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Positive SCIT response correlated with lower baseline age and higher symptom scores, allergen-specific IgE (sIgE) levels, and sIgE/total IgE (tIgE) ratio. Pi analysis revealed that elevated pre-treatment nasal sIgE levels and higher sIgE/tIgE ratios for &lt;i&gt;Der p&lt;/i&gt;, &lt;i&gt;Der f&lt;/i&gt;, &lt;i&gt;Der p&lt;/i&gt; 1, and &lt;i&gt;Der p&lt;/i&gt; 2 distinguished high from low responders. Ti analysis showed that post-treatment decreases in these nasal sIgE levels correlated with improved clinical outcomes. Logistic regression showed baseline sIgE/tIgE ratios for &lt;i&gt;Der p&lt;/i&gt; and &lt;i&gt;Der f&lt;/i&gt; both in serum and nasal secretions, and &lt;i&gt;Der p&lt;/i&gt; 1 and &lt;i&gt;Der p&lt;/i&gt; 2 in serum positively correlated with clinical improvement. The sIgE/tIgE ratios of &lt;i&gt;Der p&lt;/i&gt; (0.833 vs. 0.758) and &lt;i&gt;Der f&lt;/i&gt; (0.813 vs. 0.738) in nasal secretions exhibited higher AUC values compared to serum.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Immunologic indicators in nasal secretions are potential biomarkers for the effective prediction and monitoring of early SCIT responses.&lt;/p&gt;</content:encoded>
         <dc:creator>
Xu Xu, 
Jingyun Li, 
Xu Zhang, 
Yu Song, 
Lin Xi, 
Luo Zhang, 
Yuan Zhang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Local Specific IgE Levels Can Predict and Monitor the Therapeutic Response to Subcutaneous Immunotherapy With House Dust Mite</dc:title>
         <dc:identifier>10.1002/alr.70098</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70098</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70098?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70111?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70111</guid>
         <title>Dupilumab Beyond the Airway: Decreased Morbidity in a Real‐World Analysis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 607-614, June 2026. </description>
         <dc:description>
ABSTRACT

Background
Post hoc analyses of clinical trials have characterized dupilumab's adverse effects, yet the real‐world impact in chronic rhinosinusitis with nasal polyps (CRSwNP) and asthma is not well described. This study aims to characterize the risks of lymphoma, cardiovascular events, eosinophilia, joint pain, inflammatory arthritis, and sleep apnea in dupilumab‐treated CRSwNP and/or asthma patients compared to those not taking dupilumab, and to other biologics.


Methods
This retrospective cohort study used TriNetX, a de‐identified database containing over 100 million patient records. Demographics and adverse effects associated with immunotherapy use were collected.


Results
We identified 21,249 dupilumab‐treated CRSwNP and/or asthma patients. After matching for demographics, comorbid conditions, and medication use, dupilumab was associated with a lower risk of acute myocardial infarction (RR 0.538, 95% CI 0.435–0.665), pulmonary embolism (RR 0.639, 95% CI 0.500–0.817), cerebral infarction (RR 0.716, 95% CI 0.580–0.884), venous thrombosis (RR 0.625, 95% CI 0.511–0.763), cardiovascular disease (RR 0.733, 95% CI 0.678–0.791), and sleep apnea (RR 0.891, 95% CI 0.818–0.970), with a higher risk of eosinophilia (RR 3.157, 95% CI 2.606–3.826), versus no biologic. Dupilumab was associated with a similar risk of lymphoma and musculoskeletal outcomes. Compared to omalizumab and mepolizumab, dupilumab showed a more favorable musculoskeletal and cardiovascular profile, while it demonstrated a largely similar profile to tezepelumab.


Conclusions
Despite eosinophilia, dupilumab was associated with decreased risk of major cardiovascular, thromboembolic, and sleep apnea outcomes in CRSwNP and asthma. These findings suggest dupilumab may confer protection against adverse outcomes beyond respiratory symptom control.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Post hoc analyses of clinical trials have characterized dupilumab's adverse effects, yet the real-world impact in chronic rhinosinusitis with nasal polyps (CRSwNP) and asthma is not well described. This study aims to characterize the risks of lymphoma, cardiovascular events, eosinophilia, joint pain, inflammatory arthritis, and sleep apnea in dupilumab-treated CRSwNP and/or asthma patients compared to those not taking dupilumab, and to other biologics.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This retrospective cohort study used TriNetX, a de-identified database containing over 100 million patient records. Demographics and adverse effects associated with immunotherapy use were collected.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;We identified 21,249 dupilumab-treated CRSwNP and/or asthma patients. After matching for demographics, comorbid conditions, and medication use, dupilumab was associated with a lower risk of acute myocardial infarction (RR 0.538, 95% CI 0.435–0.665), pulmonary embolism (RR 0.639, 95% CI 0.500–0.817), cerebral infarction (RR 0.716, 95% CI 0.580–0.884), venous thrombosis (RR 0.625, 95% CI 0.511–0.763), cardiovascular disease (RR 0.733, 95% CI 0.678–0.791), and sleep apnea (RR 0.891, 95% CI 0.818–0.970), with a higher risk of eosinophilia (RR 3.157, 95% CI 2.606–3.826), versus no biologic. Dupilumab was associated with a similar risk of lymphoma and musculoskeletal outcomes. Compared to omalizumab and mepolizumab, dupilumab showed a more favorable musculoskeletal and cardiovascular profile, while it demonstrated a largely similar profile to tezepelumab.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Despite eosinophilia, dupilumab was associated with decreased risk of major cardiovascular, thromboembolic, and sleep apnea outcomes in CRSwNP and asthma. These findings suggest dupilumab may confer protection against adverse outcomes beyond respiratory symptom control.&lt;/p&gt;</content:encoded>
         <dc:creator>
Emma J. Anisman, 
Spencer Short, 
Emma Tam, 
Benjamin F. Bitner, 
Abdulghafoor Alani, 
Marc Rosen, 
Mindy Rabinowitz, 
Damaris Pena Evertz, 
Elina Toskala, 
Gurston G. Nyquist
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Dupilumab Beyond the Airway: Decreased Morbidity in a Real‐World Analysis</dc:title>
         <dc:identifier>10.1002/alr.70111</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70111</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70111?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70107?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70107</guid>
         <title>The Role of Proteases in Epithelial Dysregulation in Fungal Sinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 572-581, June 2026. </description>
         <dc:description>
ABSTRACT

Background
The role of epithelial dysregulation is poorly understood in fungal sinusitis. We aimed to examine differential gene expression and quantify protease expression in sinonasal tissue from distinct patient cohorts, those with and without invasive fungal sinusitis (IFS). We hypothesized that abnormal epithelial integrity in the sinonasal mucosa of immunosuppressed IFS patients may allow for tissue invasion.


Methods
Bulk RNA sequencing was performed on tissue from eight patients from two cohorts: immunosuppressed patients with and without IFS. Evaluation of protein expression for select proteases and their inhibitors was performed on all sinonasal tissues using multiplex western blotting. To expand upon these findings, protein expression of proteases and their inhibitors was evaluated in sinonasal tissue from eight patients with non‐invasive fungal sinusitis (fungal ball).


Results
Bulk RNA sequencing identified 33 genes that were differentially regulated in immunosuppressed IFS tissue compared to those without IFS. Multiplex western blot revealed several proteases, including matrix metalloproteinases (MMPs), with increased expression in the immunosuppressed IFS cohort compared to the cohorts without IFS. Tissue inhibitors of MMPs (TIMPs) were proportionally lower in IFS patient tissue compared to the control cohorts, resulting in several abnormal IFS‐related MMP/TIMP ratios. In the non‐invasive fungal sinusitis cohort, unique MMP/TIMP ratios were dysregulated.


Conclusions
Several proteases with increased expression in immunosuppressed IFS patients may be responsible for both an appropriate immune response to the pathogen as well as epithelial barrier breakdown and subsequent fungal invasion.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The role of epithelial dysregulation is poorly understood in fungal sinusitis. We aimed to examine differential gene expression and quantify protease expression in sinonasal tissue from distinct patient cohorts, those with and without invasive fungal sinusitis (IFS). We hypothesized that abnormal epithelial integrity in the sinonasal mucosa of immunosuppressed IFS patients may allow for tissue invasion.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Bulk RNA sequencing was performed on tissue from eight patients from two cohorts: immunosuppressed patients with and without IFS. Evaluation of protein expression for select proteases and their inhibitors was performed on all sinonasal tissues using multiplex western blotting. To expand upon these findings, protein expression of proteases and their inhibitors was evaluated in sinonasal tissue from eight patients with non-invasive fungal sinusitis (fungal ball).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Bulk RNA sequencing identified 33 genes that were differentially regulated in immunosuppressed IFS tissue compared to those without IFS. Multiplex western blot revealed several proteases, including matrix metalloproteinases (MMPs), with increased expression in the immunosuppressed IFS cohort compared to the cohorts without IFS. Tissue inhibitors of MMPs (TIMPs) were proportionally lower in IFS patient tissue compared to the control cohorts, resulting in several abnormal IFS-related MMP/TIMP ratios. In the non-invasive fungal sinusitis cohort, unique MMP/TIMP ratios were dysregulated.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Several proteases with increased expression in immunosuppressed IFS patients may be responsible for both an appropriate immune response to the pathogen as well as epithelial barrier breakdown and subsequent fungal invasion.&lt;/p&gt;</content:encoded>
         <dc:creator>
Sonam Verma, 
Iris Lee, 
John S. Schneider, 
Nyssa F. Farrell, 
Peggy L. Kendall, 
Lauren T. Roland
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>The Role of Proteases in Epithelial Dysregulation in Fungal Sinusitis</dc:title>
         <dc:identifier>10.1002/alr.70107</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70107</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70107?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70108?af=R</link>
         <pubDate>Tue, 02 Jun 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-06-02T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDate>
         <prism:coverDisplayDate>Mon, 01 Jun 2026 00:00:00 -0700</prism:coverDisplayDate>
         <guid isPermaLink="false">10.1002/alr.70108</guid>
         <title>Efficacy and Safety of Biologics, Allergen Immunotherapy, and Pharmacotherapies for Moderate‐to‐Severe Allergic Rhinitis: A Network Meta‐Analysis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, Volume 16, Issue 6, Page 582-594, June 2026. </description>
         <dc:description>
ABSTRACT

Background
The management of moderate‐to‐severe allergic rhinitis (AR) is challenging given numerous advanced therapies. A comparative, evidence‐based treatment hierarchy to guide the selection of biologics, allergen immunotherapy (AIT), and advanced pharmacotherapies is critically lacking due to a paucity of head‐to‐head trials. This network meta‐analysis established a treatment hierarchy for moderate‐to‐severe AR by comparing the efficacy and safety of biologics, AIT, and key pharmacotherapies.


Methods
We analyzed 28 randomized controlled trials (13,312 participants), which evaluated the efficacy and safety of biologics (anti‐IgE, anti‐IL‐4Rα therapies), AIT (evaluated within a 6‐month time frame to ensure comparability), and key pharmacotherapies (intranasal corticosteroids alone or combined with antihistamines) for moderate‐to‐severe AR. Efficacy was assessed by changes in the Total Nasal Symptom Score (TNSS), the Total Ocular Symptom Score (TOSS), and the Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ). A treatment hierarchy was established using surface under the cumulative ranking curve (SUCRA) probabilities.


Results
For the TNSS, anti‐IL‐4Rα therapy was most effective, followed by anti‐IgE therapy and AIT, which surpassed all pharmacotherapies. The combination of intranasal corticosteroid and intranasal antihistamine ranked the highest for ocular symptoms. Anti‐IL‐4Rα therapy was also superior for improving the RQLQ. Overall, all treatments demonstrated a favorable safety profile. Biologics and AIT did not show a significant increase in adverse events risk compared to placebo.


Conclusions
This network meta‐analysis establishes the first comprehensive treatment hierarchy for moderate‐to‐severe AR. Our findings demonstrate that biologics, particularly anti‐IL‐4Rα therapy, are the most effective interventions for nasal symptom control, ranking superior to AIT and pharmacotherapies, thus providing a robust, data‐driven framework to personalize patient care.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The management of moderate-to-severe allergic rhinitis (AR) is challenging given numerous advanced therapies. A comparative, evidence-based treatment hierarchy to guide the selection of biologics, allergen immunotherapy (AIT), and advanced pharmacotherapies is critically lacking due to a paucity of head-to-head trials. This network meta-analysis established a treatment hierarchy for moderate-to-severe AR by comparing the efficacy and safety of biologics, AIT, and key pharmacotherapies.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We analyzed 28 randomized controlled trials (13,312 participants), which evaluated the efficacy and safety of biologics (anti-IgE, anti-IL-4Rα therapies), AIT (evaluated within a 6-month time frame to ensure comparability), and key pharmacotherapies (intranasal corticosteroids alone or combined with antihistamines) for moderate-to-severe AR. Efficacy was assessed by changes in the Total Nasal Symptom Score (TNSS), the Total Ocular Symptom Score (TOSS), and the Rhinoconjunctivitis Quality of Life Questionnaire (RQLQ). A treatment hierarchy was established using surface under the cumulative ranking curve (SUCRA) probabilities.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;For the TNSS, anti-IL-4Rα therapy was most effective, followed by anti-IgE therapy and AIT, which surpassed all pharmacotherapies. The combination of intranasal corticosteroid and intranasal antihistamine ranked the highest for ocular symptoms. Anti-IL-4Rα therapy was also superior for improving the RQLQ. Overall, all treatments demonstrated a favorable safety profile. Biologics and AIT did not show a significant increase in adverse events risk compared to placebo.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;This network meta-analysis establishes the first comprehensive treatment hierarchy for moderate-to-severe AR. Our findings demonstrate that biologics, particularly anti-IL-4Rα therapy, are the most effective interventions for nasal symptom control, ranking superior to AIT and pharmacotherapies, thus providing a robust, data-driven framework to personalize patient care.&lt;/p&gt;</content:encoded>
         <dc:creator>
Zengxiao Zhang, 
Dandan Fang, 
Chengshuo Wang, 
Yuan Zhang, 
Luo Zhang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Efficacy and Safety of Biologics, Allergen Immunotherapy, and Pharmacotherapies for Moderate‐to‐Severe Allergic Rhinitis: A Network Meta‐Analysis</dc:title>
         <dc:identifier>10.1002/alr.70108</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70108</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70108?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
         <prism:volume>16</prism:volume>
         <prism:number>6</prism:number>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70191?af=R</link>
         <pubDate>Mon, 01 Jun 2026 08:21:22 -0700</pubDate>
         <dc:date>2026-06-01T08:21:22-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70191</guid>
         <title>Assessing Surgical Extent in Endoscopic Sinus Surgery: A Scoping Review of Scoring Systems</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Endoscopic sinus surgery (ESS) varies substantially in the extent of surgical dissection performed, even when described under the same procedural label. In chronic rhinosinusitis, this heterogeneity may influence postoperative outcomes, revision rates, and response to biologic therapies. This review aimed to identify and characterize available instruments for assessing surgical extent after ESS.


Methods
Scoping review following PRISMA‐ScR guidelines with systematic search of PubMed/MEDLINE, Scopus, and Web of Science.


Results
Twenty‐one studies describing 11 instruments were included: spanning computed tomography (CT)‐based scores (Amsterdam Classification of Completeness of Endoscopic Sinus Surgery [ACCESS], Completion of Surgery Index [CoSI], Sinus Surgery Completeness Score [SSCS], and Residual Ethmoid Cell [REC] score), intraoperative classifications (Lamella–Ostium–Extent–Mucosa [LOEM], complete vs. targeted, and Japanese Rhinologic Society [JRS]), radiologic–surgical concordance metrics, and study‐specific tools. A key conceptual distinction emerged between surgical extent (the procedure performed) and surgical completeness (the anatomical result achieved). CT‐based instruments primarily assess completeness, whereas intraoperative classifications capture extent. Because similar procedures may yield different anatomical results, these dimensions are not interchangeable. Among CT‐based instruments, CoSI demonstrated the most consistent outcome associations, with incomplete prior surgery predicting greater benefit from revision ESS. ACCESS showed preliminary utility in biologic response prediction. LOEM is the only intraoperative system with reported outcome associations, although evidence is limited to a single group. Overall, evidence across instruments remains limited and predominantly retrospective.


Conclusions
CT‐based and intraoperative instruments capture different dimensions of prior surgery and should be selected according to the clinical or research question. Notably, structured scoring consistently reveals that many patients meeting guideline criteria for prior surgery have varying anatomical dissection. Given the association between surgical extent, postoperative outcomes, and biologic therapy response, its standardized assessment warrants evaluation for integration into clinical decision making. However, prospective validation is urgently needed.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Endoscopic sinus surgery (ESS) varies substantially in the extent of surgical dissection performed, even when described under the same procedural label. In chronic rhinosinusitis, this heterogeneity may influence postoperative outcomes, revision rates, and response to biologic therapies. This review aimed to identify and characterize available instruments for assessing surgical extent after ESS.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Scoping review following PRISMA-ScR guidelines with systematic search of PubMed/MEDLINE, Scopus, and Web of Science.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Twenty-one studies describing 11 instruments were included: spanning computed tomography (CT)-based scores (Amsterdam Classification of Completeness of Endoscopic Sinus Surgery [ACCESS], Completion of Surgery Index [CoSI], Sinus Surgery Completeness Score [SSCS], and Residual Ethmoid Cell [REC] score), intraoperative classifications (Lamella–Ostium–Extent–Mucosa [LOEM], complete vs. targeted, and Japanese Rhinologic Society [JRS]), radiologic–surgical concordance metrics, and study-specific tools. A key conceptual distinction emerged between surgical extent (the procedure performed) and surgical completeness (the anatomical result achieved). CT-based instruments primarily assess completeness, whereas intraoperative classifications capture extent. Because similar procedures may yield different anatomical results, these dimensions are not interchangeable. Among CT-based instruments, CoSI demonstrated the most consistent outcome associations, with incomplete prior surgery predicting greater benefit from revision ESS. ACCESS showed preliminary utility in biologic response prediction. LOEM is the only intraoperative system with reported outcome associations, although evidence is limited to a single group. Overall, evidence across instruments remains limited and predominantly retrospective.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;CT-based and intraoperative instruments capture different dimensions of prior surgery and should be selected according to the clinical or research question. Notably, structured scoring consistently reveals that many patients meeting guideline criteria for prior surgery have varying anatomical dissection. Given the association between surgical extent, postoperative outcomes, and biologic therapy response, its standardized assessment warrants evaluation for integration into clinical decision making. However, prospective validation is urgently needed.&lt;/p&gt;</content:encoded>
         <dc:creator>
Alexander Lein, 
Marie T. Ehrgott, 
Linda Liu, 
Archana Jaiswal, 
Rajiv K. Bhalla, 
Noel Ayoub, 
Faris F. Brkic, 
David T. Liu
</dc:creator>
         <category>REVIEW ARTICLE</category>
         <dc:title>Assessing Surgical Extent in Endoscopic Sinus Surgery: A Scoping Review of Scoring Systems</dc:title>
         <dc:identifier>10.1002/alr.70191</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70191</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70191?af=R</prism:url>
         <prism:section>REVIEW ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70181?af=R</link>
         <pubDate>Mon, 01 Jun 2026 08:20:46 -0700</pubDate>
         <dc:date>2026-06-01T08:20:46-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70181</guid>
         <title>AI‐Based Quantitative Nasal Cytology for Predicting Eosinophilic Chronic Rhinosinusitis With Nasal Polyps: A Pilot Study</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Jiaying Li, 
Xu Zhang, 
Zengxiao Zhang, 
Yu Song, 
Xu Xu, 
Luo Zhang, 
Yuan Zhang
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>AI‐Based Quantitative Nasal Cytology for Predicting Eosinophilic Chronic Rhinosinusitis With Nasal Polyps: A Pilot Study</dc:title>
         <dc:identifier>10.1002/alr.70181</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70181</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70181?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70196?af=R</link>
         <pubDate>Mon, 01 Jun 2026 08:19:36 -0700</pubDate>
         <dc:date>2026-06-01T08:19:36-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70196</guid>
         <title>Impact of Genetic and Molecular Alterations on Clinical Outcomes in Sinonasal Squamous Cell Carcinoma: A Systematic Review and Meta‐Analysis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Sinonasal squamous cell carcinoma (SNSCC) is a rare malignancy with variable outcomes, and the prognostic impact of molecular alterations remains incompletely defined. This meta‐analysis aims to clarify the associations of genetic alterations and protein expression with clinical outcomes in SNSCC.


Methods
PubMed, Embase, Web of Science, and ScienceDirect were searched from inception through February 2026. Eligible studies reported prognostic outcomes in SNSCC according to EGFR mutation, TP53 mutation, EGFR copy number gain, EGFR‐associated progression from inverted papilloma to SNSCC, DEK::AFF2 alteration, or expression of EGFR, p53, Foxp3, SOX2, KMT2D, PD‐L1, and Bax. Random‐effects models were used to pool survival or recurrence rates and hazard ratios (HRs) with 95% confidence intervals.


Results
Of 689 records, 25 retrospective cohort studies including at least 1194 patients with SNSCC were analyzed. Median age was 63.8 years, 69.7% were male, and median follow‐up was 33 months. EGFR mutation was associated with worse overall survival (OS) at 2, 3, 5, and 10 years (HRs 1.57, 1.49, 1.41, and 1.32, respectively) and worse disease‐free survival (DFS) at 1 and 3 years (HRs 3.70 and 1.51). TP53 mutation was associated with worse OS at 2, 3, and 5 years (HRs 3.54, 3.33, and 2.70). EGFR copy number gain was associated with worse 5‐year OS (HR 1.59), EGFR overexpression with higher regional recurrence (HR 2.69), and PD‐L1 expression with worse 3‐year OS (HR 1.43). In contrast, Foxp3 expression was associated with improved 2‐, 3‐, and 5‐year OS (HRs 0.42, 0.51, and 0.53) and DFS (HRs 0.48, 0.48, and 0.50). Other biomarkers, such as SOX2, Bax, p53 overexpression, and KMT2D expression, were not significantly associated with prognosis.


Conclusion
Molecular profiling has prognostic value in SNSCC. EGFR and TP53 alterations were associated with poorer outcomes, whereas Foxp3 expression was associated with more favorable survival, supporting further biomarker‐integrated risk stratification in SNSCC.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Sinonasal squamous cell carcinoma (SNSCC) is a rare malignancy with variable outcomes, and the prognostic impact of molecular alterations remains incompletely defined. This meta-analysis aims to clarify the associations of genetic alterations and protein expression with clinical outcomes in SNSCC.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;PubMed, Embase, Web of Science, and ScienceDirect were searched from inception through February 2026. Eligible studies reported prognostic outcomes in SNSCC according to EGFR mutation, TP53 mutation, EGFR copy number gain, EGFR-associated progression from inverted papilloma to SNSCC, DEK::AFF2 alteration, or expression of EGFR, p53, Foxp3, SOX2, KMT2D, PD-L1, and Bax. Random-effects models were used to pool survival or recurrence rates and hazard ratios (HRs) with 95% confidence intervals.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Of 689 records, 25 retrospective cohort studies including at least 1194 patients with SNSCC were analyzed. Median age was 63.8 years, 69.7% were male, and median follow-up was 33 months. EGFR mutation was associated with worse overall survival (OS) at 2, 3, 5, and 10 years (HRs 1.57, 1.49, 1.41, and 1.32, respectively) and worse disease-free survival (DFS) at 1 and 3 years (HRs 3.70 and 1.51). TP53 mutation was associated with worse OS at 2, 3, and 5 years (HRs 3.54, 3.33, and 2.70). EGFR copy number gain was associated with worse 5-year OS (HR 1.59), EGFR overexpression with higher regional recurrence (HR 2.69), and PD-L1 expression with worse 3-year OS (HR 1.43). In contrast, Foxp3 expression was associated with improved 2-, 3-, and 5-year OS (HRs 0.42, 0.51, and 0.53) and DFS (HRs 0.48, 0.48, and 0.50). Other biomarkers, such as SOX2, Bax, p53 overexpression, and KMT2D expression, were not significantly associated with prognosis.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Molecular profiling has prognostic value in SNSCC. EGFR and TP53 alterations were associated with poorer outcomes, whereas Foxp3 expression was associated with more favorable survival, supporting further biomarker-integrated risk stratification in SNSCC.&lt;/p&gt;</content:encoded>
         <dc:creator>
Srivatsa Surya Vasudevan, 
Amber Cradeur, 
Madeline Polson, 
Cherie‐Ann O. Nathan, 
Omar G. Ahmed, 
Michael T. Yim
</dc:creator>
         <category>REVIEW ARTICLE</category>
         <dc:title>Impact of Genetic and Molecular Alterations on Clinical Outcomes in Sinonasal Squamous Cell Carcinoma: A Systematic Review and Meta‐Analysis</dc:title>
         <dc:identifier>10.1002/alr.70196</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70196</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70196?af=R</prism:url>
         <prism:section>REVIEW ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70193?af=R</link>
         <pubDate>Thu, 28 May 2026 06:09:42 -0700</pubDate>
         <dc:date>2026-05-28T06:09:42-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70193</guid>
         <title>Wearable Real‐Time Translation in Rhinology: A Comparative Study of Accuracy and Efficiency</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Emma J. Anisman, 
Nickolas Pudik, 
Laura Palacio‐Morales, 
Abdulghafoor Alani, 
Yanmin Qu, 
Chang Liu, 
Agustina Arce, 
Shin Heng Teresa Chan, 
Benjamin Bitner, 
Marc Rosen, 
Gurston Nyquist, 
Elina Toskala, 
Mindy Rabinowitz
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Wearable Real‐Time Translation in Rhinology: A Comparative Study of Accuracy and Efficiency</dc:title>
         <dc:identifier>10.1002/alr.70193</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70193</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70193?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70192?af=R</link>
         <pubDate>Thu, 28 May 2026 06:04:31 -0700</pubDate>
         <dc:date>2026-05-28T06:04:31-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70192</guid>
         <title>Effects of Sinonasal Mucus Debridement on Nasal Nitric Oxide in Primary Ciliary Dyskinesia</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Nathan R. Barefoot, 
John B. Henrich, 
Elena Quinonez Del Cid, 
Priya J. Desai, 
Katrina Bootes, 
Jackson Vuncannon, 
Cristine Klatt‐Cromwell, 
Brian D. Thorp, 
Charles S. Ebert Jr, 
Brent A. Senior, 
Lawrence Ostroswki, 
Adam J. Kimple
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Effects of Sinonasal Mucus Debridement on Nasal Nitric Oxide in Primary Ciliary Dyskinesia</dc:title>
         <dc:identifier>10.1002/alr.70192</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70192</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70192?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70188?af=R</link>
         <pubDate>Wed, 27 May 2026 01:13:08 -0700</pubDate>
         <dc:date>2026-05-27T01:13:08-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70188</guid>
         <title>In Response to the Letter to the Editor: “Methodological Considerations in Interpreting Quality‐of‐Life Recovery in C19OD”</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Tiana M. Saak, 
Jonathan B. Overdevest
</dc:creator>
         <category>REPLY</category>
         <dc:title>In Response to the Letter to the Editor: “Methodological Considerations in Interpreting Quality‐of‐Life Recovery in C19OD”</dc:title>
         <dc:identifier>10.1002/alr.70188</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70188</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70188?af=R</prism:url>
         <prism:section>REPLY</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70189?af=R</link>
         <pubDate>Wed, 27 May 2026 01:13:07 -0700</pubDate>
         <dc:date>2026-05-27T01:13:07-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70189</guid>
         <title>Lower Airway Conditions Contribute to the Prediction of Polyp Recurrence in Chronic Rhinosinusitis With Nasal Polyps and Comorbid Asthma</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>

Key Points

Duration of asthma, ratio of peak expiratory flow to predicted value, and ratio of maximal expiratory flow at 25% of the vital capacity to predicted value are independent risk factors for polyp recurrence in patients with CRSwNP+AS.
A lower+upper model created with the ethmoid sinus score and the three lower airway factors shows good predictive value for polyp recurrence in patients with CRSwNP+AS.


</dc:description>
         <content:encoded>
&lt;h2&gt;Key Points&lt;/h2&gt;
&lt;p&gt;
Duration of asthma, ratio of peak expiratory flow to predicted value, and ratio of maximal expiratory flow at 25% of the vital capacity to predicted value are independent risk factors for polyp recurrence in patients with CRSwNP+AS.
A lower+upper model created with the ethmoid sinus score and the three lower airway factors shows good predictive value for polyp recurrence in patients with CRSwNP+AS.
&lt;/p&gt;</content:encoded>
         <dc:creator>
Jiaxing Guo, 
Jing Yuan, 
Yu Hong, 
Zhou Yu, 
Xiaomo Wang, 
Chengshuo Wang, 
Aihui Yan, 
Luo Zhang, 
Ming Wang
</dc:creator>
         <category>RESEARCH NOTE</category>
         <dc:title>Lower Airway Conditions Contribute to the Prediction of Polyp Recurrence in Chronic Rhinosinusitis With Nasal Polyps and Comorbid Asthma</dc:title>
         <dc:identifier>10.1002/alr.70189</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70189</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70189?af=R</prism:url>
         <prism:section>RESEARCH NOTE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70190?af=R</link>
         <pubDate>Wed, 27 May 2026 01:11:54 -0700</pubDate>
         <dc:date>2026-05-27T01:11:54-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70190</guid>
         <title>Site‐Specific Olfactory Cleft Opacification Predicts Olfactory Function and Olfactory Training Outcome in Persistent Postinfection Olfactory Dysfunction</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Persistent postinfectious olfactory dysfunction (PIOD) is a prevalent and often refractory condition, with low recovery rates following olfactory training (OT), primarily due to sustained localized inflammation and opacification within the olfactory cleft (OC). However, conventional radiological assessments of OC opacification overlook the vertical distribution of olfactory neuroepithelium, limiting prognostic accuracy. This study introduces a modified subregion computed tomography (CT) scoring system integrated with computational fluid dynamics (CFD) to evaluate OC opacification's role in baseline olfaction and OT efficacy.


Methods
In this prospective study, 58 adults with persistent PIOD of more than 3 months’ duration were enrolled and completed CT imaging, psychophysical olfactory testing (Sniffin’ Sticks TDI score), and questionnaire assessments. Using a modified scoring system, the OC was segmented on coronal sections into upper (superior one‐third) and lower (inferior two‐thirds) portions, with three coronal sections assessed in both the anterior and posterior OC. Each section was scored dichotomously (0 for no opacification, 1 for opacification), and bilateral scores were recorded. Unsupervised K‐means clustering identified phenotypes, random forest modeling predicted functional anosmia, and CFD analyzed airflow dynamics. Thirty‐one patients completed 3‐month OT with follow‐up assessments.


Results
OC opacification was present in 69.0% of persistent PIOD patients, with opacification in the upper posterior OC notably serving as the primary determinant of baseline olfactory function. Random forest analysis further confirmed that upper OC opacification ranked as the top predictor for functional anosmia, with the combined model achieving an area under the curve of 0.920. Cluster analysis revealed three distinct phenotypes, among which the diffuse severe opacification cluster involving upper OC regions was associated with the poorest olfactory function. Although posterior OC opacification was positively correlated with increased airflow velocity ratios (r = 0.570, p &lt; 0.01) and these ratios were negatively correlated with olfactory scores, OC airflow itself did not significantly mediate the relationship between structure and olfactory function. Only 25.8% of patients achieved clinically meaningful olfactory improvement. Significant improvements were observed in TDI (p = 0.001), olfactory threshold (p = 0.010), olfactory discrimination (p = 0.028), and olfactory VAS scores (p &lt; 0.001) after OT. Baseline opacification in posterior‐middle section of OC significantly predicted non‐response.


Conclusions
The modified subregion OC opacification scoring system provides a more refined assessment of site‑specific OC obstruction for patients with persistent PIOD, underscoring the critical role of OC opacification in mediating olfactory impairment and resistance to OT.


Clinical Implication
For patients with persistent PIOD, this modified olfactory cleft opacification scoring system allows for olfactory assessment and prognosis by identifying specific opacification patterns associated with olfactory training outcomes.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Persistent postinfectious olfactory dysfunction (PIOD) is a prevalent and often refractory condition, with low recovery rates following olfactory training (OT), primarily due to sustained localized inflammation and opacification within the olfactory cleft (OC). However, conventional radiological assessments of OC opacification overlook the vertical distribution of olfactory neuroepithelium, limiting prognostic accuracy. This study introduces a modified subregion computed tomography (CT) scoring system integrated with computational fluid dynamics (CFD) to evaluate OC opacification's role in baseline olfaction and OT efficacy.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;In this prospective study, 58 adults with persistent PIOD of more than 3 months’ duration were enrolled and completed CT imaging, psychophysical olfactory testing (Sniffin’ Sticks TDI score), and questionnaire assessments. Using a modified scoring system, the OC was segmented on coronal sections into upper (superior one-third) and lower (inferior two-thirds) portions, with three coronal sections assessed in both the anterior and posterior OC. Each section was scored dichotomously (0 for no opacification, 1 for opacification), and bilateral scores were recorded. Unsupervised &lt;i&gt;K&lt;/i&gt;-means clustering identified phenotypes, random forest modeling predicted functional anosmia, and CFD analyzed airflow dynamics. Thirty-one patients completed 3-month OT with follow-up assessments.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;OC opacification was present in 69.0% of persistent PIOD patients, with opacification in the upper posterior OC notably serving as the primary determinant of baseline olfactory function. Random forest analysis further confirmed that upper OC opacification ranked as the top predictor for functional anosmia, with the combined model achieving an area under the curve of 0.920. Cluster analysis revealed three distinct phenotypes, among which the diffuse severe opacification cluster involving upper OC regions was associated with the poorest olfactory function. Although posterior OC opacification was positively correlated with increased airflow velocity ratios (&lt;i&gt;r&lt;/i&gt; = 0.570, &lt;i&gt;p &lt;/i&gt;&amp;lt; 0.01) and these ratios were negatively correlated with olfactory scores, OC airflow itself did not significantly mediate the relationship between structure and olfactory function. Only 25.8% of patients achieved clinically meaningful olfactory improvement. Significant improvements were observed in TDI (&lt;i&gt;p&lt;/i&gt; = 0.001), olfactory threshold (&lt;i&gt;p&lt;/i&gt; = 0.010), olfactory discrimination (&lt;i&gt;p&lt;/i&gt; = 0.028), and olfactory VAS scores (&lt;i&gt;p &lt;/i&gt;&amp;lt; 0.001) after OT. Baseline opacification in posterior-middle section of OC significantly predicted non-response.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;The modified subregion OC opacification scoring system provides a more refined assessment of site‑specific OC obstruction for patients with persistent PIOD, underscoring the critical role of OC opacification in mediating olfactory impairment and resistance to OT.&lt;/p&gt;
&lt;h2&gt;Clinical Implication&lt;/h2&gt;
&lt;p&gt;For patients with persistent PIOD, this modified olfactory cleft opacification scoring system allows for olfactory assessment and prognosis by identifying specific opacification patterns associated with olfactory training outcomes.&lt;/p&gt;</content:encoded>
         <dc:creator>
Yankun Li, 
Lina Chen, 
Yunfan Zhang, 
Chia‐Yi Lin, 
Xincen Jiang, 
Shilong Sun, 
Hailing Jiang, 
Xinyi Ge, 
Zhidi Zhang, 
Hongping Fu, 
Yinghong Zhang, 
Dawei Wu
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Site‐Specific Olfactory Cleft Opacification Predicts Olfactory Function and Olfactory Training Outcome in Persistent Postinfection Olfactory Dysfunction</dc:title>
         <dc:identifier>10.1002/alr.70190</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70190</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70190?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70187?af=R</link>
         <pubDate>Wed, 27 May 2026 01:10:55 -0700</pubDate>
         <dc:date>2026-05-27T01:10:55-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70187</guid>
         <title>Endoscopically Confirmed False‐Positive β2‐Transferrin in the Postoperative Setting</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Noah Overbeck, 
Somtochi Okafor, 
Erin Yamamoto, 
Olabisi Sanusi, 
Mathew Geltzeiler
</dc:creator>
         <category>CLINICAL LETTER</category>
         <dc:title>Endoscopically Confirmed False‐Positive β2‐Transferrin in the Postoperative Setting</dc:title>
         <dc:identifier>10.1002/alr.70187</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70187</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70187?af=R</prism:url>
         <prism:section>CLINICAL LETTER</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70186?af=R</link>
         <pubDate>Wed, 27 May 2026 01:10:24 -0700</pubDate>
         <dc:date>2026-05-27T01:10:24-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70186</guid>
         <title>Letter to the Editor Regarding “Recovery of Parosmia Preferentially Influences Longitudinal Improvement of Quality of Life in C19OD”</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description/>
         <content:encoded/>
         <dc:creator>
Pei‐Shan Li
</dc:creator>
         <category>LETTER TO THE EDITOR</category>
         <dc:title>Letter to the Editor Regarding “Recovery of Parosmia Preferentially Influences Longitudinal Improvement of Quality of Life in C19OD”</dc:title>
         <dc:identifier>10.1002/alr.70186</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70186</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70186?af=R</prism:url>
         <prism:section>LETTER TO THE EDITOR</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70184?af=R</link>
         <pubDate>Wed, 13 May 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-05-13T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70184</guid>
         <title>Chronic Rhinosinusitis With Nasal Polyposis in EGPA: A Real‐Life Multidimensional Analysis Through Mepolizumab Dosing and Role of Adjunctive Endoscopic Sinus Surgery (ESS)</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare necrotizing vasculitis involving upper‐ and lower‐airways. Despite biologics, sinonasal disease often persists. Evidence on ENT trajectories under anti‐IL5 treatment and role of endoscopic sinus surgery (ESS) remains limited and is often described without standardized assessment tools. This study provides a systematic, multidimensional evaluation of sinonasal outcomes under biologic therapy and analyzes the role of ESS in a real‐life cohort.


Methods
We retrospectively analyzed 52 EGPA patients with a 24‐month follow‐up on mepolizumab. Sinonasal disease was assessed by Nasal Polyp Score (NPS), Lund–Kennedy Score (LKS), Lund–Mackay score (LMK), and SNOT‐22, while systemic activity was assessed by Birmingham Vasculitis Activity Score (BVAS). Patients were stratified by mepolizumab regimen (100 mg, 300 mg, and step‐down). Predictors of adjunctive ESS were explored through multivariate logistic regression.


Results
Systemic remission occurred in &gt;90% of patients, with marked eosinophil suppression (median 700 → 59.5 cells/µL) and BVAS = 0. Conversely, NPS and LKS remained stable [IQR]: (NPS 4 [3–5] → 4 [2–5]; LKS 6 [4–8] → 5 [2–7.75]. Polyps persisted in 64% and mucosal edema/discharge in 92% of population. Continuous 100 mg therapy showed the greatest endoscopic improvement. Higher baseline sinonasal burden, more extensive surgical history, and mepolizumab dose variation were associated with adjunctive ESS (28.8%), whereas BVAS and eosinophils showed no correlation with ENT severity.


Conclusion
Sinonasal disease may persist despite systemic remission, suggesting a partially independent inflammatory niche. Comprehensive assessment should combine systemic markers with dedicated ENT evaluation, while management may require integrated biologic–surgical strategies in chronic structural disease.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare necrotizing vasculitis involving upper- and lower-airways. Despite biologics, sinonasal disease often persists. Evidence on ENT trajectories under anti-IL5 treatment and role of endoscopic sinus surgery (ESS) remains limited and is often described without standardized assessment tools. This study provides a systematic, multidimensional evaluation of sinonasal outcomes under biologic therapy and analyzes the role of ESS in a real-life cohort.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We retrospectively analyzed 52 EGPA patients with a 24-month follow-up on mepolizumab. Sinonasal disease was assessed by Nasal Polyp Score (NPS), Lund–Kennedy Score (LKS), Lund–Mackay score (LMK), and SNOT-22, while systemic activity was assessed by Birmingham Vasculitis Activity Score (BVAS). Patients were stratified by mepolizumab regimen (100 mg, 300 mg, and &lt;i&gt;step-down&lt;/i&gt;). Predictors of adjunctive ESS were explored through multivariate logistic regression.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Systemic remission occurred in &amp;gt;90% of patients, with marked eosinophil suppression (median 700 → 59.5 cells/µL) and BVAS = 0. Conversely, NPS and LKS remained stable [IQR]: (NPS 4 [3–5] → 4 [2–5]; LKS 6 [4–8] → 5 [2–7.75]. Polyps persisted in 64% and mucosal edema/discharge in 92% of population. Continuous 100 mg therapy showed the greatest endoscopic improvement. Higher baseline sinonasal burden, more extensive surgical history, and mepolizumab dose variation were associated with adjunctive ESS (28.8%), whereas BVAS and eosinophils showed no correlation with ENT severity.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Sinonasal disease may persist despite systemic remission, suggesting a partially independent inflammatory niche. Comprehensive assessment should combine systemic markers with dedicated ENT evaluation, while management may require integrated biologic–surgical strategies in chronic structural disease.&lt;/p&gt;</content:encoded>
         <dc:creator>
Bright Oworae Howardson, 
Giulia Danè, 
Luca Moroni, 
Marco Lanzillotta, 
Umberto Tanzini, 
Gabriele D. Gallina, 
Adriana Cariddi, 
Biancamaria Venerandi, 
Lorenzo Dagna, 
Leone Giordano, 
Apostolos Karligkiotis
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Chronic Rhinosinusitis With Nasal Polyposis in EGPA: A Real‐Life Multidimensional Analysis Through Mepolizumab Dosing and Role of Adjunctive Endoscopic Sinus Surgery (ESS)</dc:title>
         <dc:identifier>10.1002/alr.70184</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70184</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70184?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70183?af=R</link>
         <pubDate>Tue, 12 May 2026 04:30:32 -0700</pubDate>
         <dc:date>2026-05-12T04:30:32-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70183</guid>
         <title>Female‐Specific Risk of TAS2R Variants in Chronic Rhinosinusitis: A Hospital‐Based Cohort Study From the Taiwan Precision Medicine Initiative</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Bitter taste receptors (T2Rs) function in the innate immune defense of the sinonasal mucosa; however, the genetic association between the TAS2R gene family and chronic rhinosinusitis (CRS) remains understudied in Asian populations. This study aimed to investigate the impact of these genetic variants on CRS susceptibility using a large East Asian Han Chinese genomic database.


Methods
This retrospective case‒control study analyzed the Taiwan Precision Medicine Initiative dataset. We included 826 patients with CRS and 8260 control subjects. Controls were screened using ICD codes to exclude other upper airway disorders and were matched 1:10 to cases by age and sex. Univariable and multivariable logistic regression models, adjusted for relevant clinical covariates, were used to evaluate the independent effects of TAS2R genetic variants. We also conducted stratified analyses based on biological sex and clinical CRS phenotypes.


Results
Multivariable analysis identified TAS2R38 (rs77730028: adjusted odds ratio [aOR] = 1.363, p &lt; 0.001) and TAS2R42 (rs1669424: aOR = 1.143, p = 0.039) as independent risk factors for CRS, whereas TAS2R1 (rs385: aOR = 0.912, p = 0.019) demonstrated a significant protective effect. Our study revealed a marked sexual dimorphism: these genetic associations were almost exclusively driven by the female cohort (in females, the risk effect of TAS2R38 reached an aOR of 1.709, p &lt; 0.001, with no significant association observed in males). The risk effect of TAS2R38 remained consistent across both patients with CRS with nasal polyps and those without nasal polyps.


Conclusion
Genetic variations within the TAS2R family significantly influence the risk of developing CRS in the Han Chinese population, demonstrating a specific female‐driven effect. These findings help classify CRS endotypes and suggest that biological sex should be considered in future precision medicine and targeted therapeutic strategies.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Bitter taste receptors (T2Rs) function in the innate immune defense of the sinonasal mucosa; however, the genetic association between the &lt;i&gt;TAS2R&lt;/i&gt; gene family and chronic rhinosinusitis (CRS) remains understudied in Asian populations. This study aimed to investigate the impact of these genetic variants on CRS susceptibility using a large East Asian Han Chinese genomic database.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This retrospective case‒control study analyzed the Taiwan Precision Medicine Initiative dataset. We included 826 patients with CRS and 8260 control subjects. Controls were screened using ICD codes to exclude other upper airway disorders and were matched 1:10 to cases by age and sex. Univariable and multivariable logistic regression models, adjusted for relevant clinical covariates, were used to evaluate the independent effects of &lt;i&gt;TAS2R&lt;/i&gt; genetic variants. We also conducted stratified analyses based on biological sex and clinical CRS phenotypes.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Multivariable analysis identified &lt;i&gt;TAS2R38&lt;/i&gt; (rs77730028: adjusted odds ratio [aOR] = 1.363, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001) and &lt;i&gt;TAS2R42&lt;/i&gt; (rs1669424: aOR = 1.143, &lt;i&gt;p&lt;/i&gt; = 0.039) as independent risk factors for CRS, whereas &lt;i&gt;TAS2R1&lt;/i&gt; (rs385: aOR = 0.912, &lt;i&gt;p&lt;/i&gt; = 0.019) demonstrated a significant protective effect. Our study revealed a marked sexual dimorphism: these genetic associations were almost exclusively driven by the female cohort (in females, the risk effect of &lt;i&gt;TAS2R38&lt;/i&gt; reached an aOR of 1.709, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001, with no significant association observed in males). The risk effect of &lt;i&gt;TAS2R38&lt;/i&gt; remained consistent across both patients with CRS with nasal polyps and those without nasal polyps.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Genetic variations within the &lt;i&gt;TAS2R&lt;/i&gt; family significantly influence the risk of developing CRS in the Han Chinese population, demonstrating a specific female-driven effect. These findings help classify CRS endotypes and suggest that biological sex should be considered in future precision medicine and targeted therapeutic strategies.&lt;/p&gt;</content:encoded>
         <dc:creator>
Rong‐San Jiang, 
Man‐Wei Hua, 
I‐Chieh Chen, 
Yi‐Ming Chen, 
Shun‐Hung Lin, 
Kuan‐Yu Lai, 
Yi‐Chen Chen
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Female‐Specific Risk of TAS2R Variants in Chronic Rhinosinusitis: A Hospital‐Based Cohort Study From the Taiwan Precision Medicine Initiative</dc:title>
         <dc:identifier>10.1002/alr.70183</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70183</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70183?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70182?af=R</link>
         <pubDate>Mon, 11 May 2026 08:19:58 -0700</pubDate>
         <dc:date>2026-05-11T08:19:58-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70182</guid>
         <title>Lost and Found: Is Olfactory Recovery More Promising After COVID‐19 Than Other Causes, Even 2 Years Later?</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Olfactory dysfunction is a hallmark feature of COVID‐19, yet the potential for recovery with long‐standing COVID‐19‐related smell loss (CRSL) remains uncertain, particularly when treatment is initiated years later. This study evaluated olfactory outcomes in patients with CRSL compared with non‐COVID‐19‐related smell loss (non‐CRSL), with emphasis on delayed treatment initiation.


Methods
This retrospective cohort study included 104 patients evaluated at a tertiary clinic between January 2023 and February 2025, comprising 47 patients with CRSL and 57 with non‐CRSL. All patients completed serial Sniffin’ Sticks testing (threshold, discrimination, and identification [TDI]) at ≥2 visits. Minimal clinically important difference (MCID) was defined as a ≥5.5‐point increase in TDI score. All patients received olfactory training combined with twice‐daily steroid nasal irrigation. Subgroup analyses examined delayed treatment initiation (&gt;2 years), treatment adherence, and COVID‐19 vaccination status.


Results
Baseline TDI scores were higher in the CRSL group than in the non‐CRSL group (19.6 ± 6.3 vs. 16.8 ± 6.8; p &lt; 0.05). The CRSL group demonstrated significant improvement in TDI scores at follow‐up (19.6 ± 6.3 to 23.9 ± 6.5; p &lt; 0.001), with 46% achieving MCID, whereas the non‐CRSL group showed no significant change. Among CRSL patients initiating therapy &gt;2 years after onset (n = 36; mean 30.8 ± 5.5 months), 50% achieved MCID. Treatment adherence was strongly associated with improvement, whereas COVID‐19 vaccination showed a favorable but attenuated association after adjustment.


Conclusions
Clinically meaningful olfactory recovery remains achievable with long‐standing CRSL, even when treatment is initiated &gt;2 years after onset. Prospective studies are needed to clarify causal relationships given known spontaneous recovery in post‐viral olfactory dysfunction.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Olfactory dysfunction is a hallmark feature of COVID-19, yet the potential for recovery with long-standing COVID-19-related smell loss (CRSL) remains uncertain, particularly when treatment is initiated years later. This study evaluated olfactory outcomes in patients with CRSL compared with non-COVID-19-related smell loss (non-CRSL), with emphasis on delayed treatment initiation.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This retrospective cohort study included 104 patients evaluated at a tertiary clinic between January 2023 and February 2025, comprising 47 patients with CRSL and 57 with non-CRSL. All patients completed serial Sniffin’ Sticks testing (threshold, discrimination, and identification [TDI]) at ≥2 visits. Minimal clinically important difference (MCID) was defined as a ≥5.5-point increase in TDI score. All patients received olfactory training combined with twice-daily steroid nasal irrigation. Subgroup analyses examined delayed treatment initiation (&amp;gt;2 years), treatment adherence, and COVID-19 vaccination status.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Baseline TDI scores were higher in the CRSL group than in the non-CRSL group (19.6 ± 6.3 vs. 16.8 ± 6.8; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). The CRSL group demonstrated significant improvement in TDI scores at follow-up (19.6 ± 6.3 to 23.9 ± 6.5; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), with 46% achieving MCID, whereas the non-CRSL group showed no significant change. Among CRSL patients initiating therapy &amp;gt;2 years after onset (&lt;i&gt;n&lt;/i&gt; = 36; mean 30.8 ± 5.5 months), 50% achieved MCID. Treatment adherence was strongly associated with improvement, whereas COVID-19 vaccination showed a favorable but attenuated association after adjustment.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Clinically meaningful olfactory recovery remains achievable with long-standing CRSL, even when treatment is initiated &amp;gt;2 years after onset. Prospective studies are needed to clarify causal relationships given known spontaneous recovery in post-viral olfactory dysfunction.&lt;/p&gt;</content:encoded>
         <dc:creator>
John W. Hunsicker, 
Mabel Berg, 
Nicolaus Knight, 
Jessica W. Grayson, 
Bradford A. Woodworth, 
Justin H. Turner, 
Do‐Yeon Cho
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Lost and Found: Is Olfactory Recovery More Promising After COVID‐19 Than Other Causes, Even 2 Years Later?</dc:title>
         <dc:identifier>10.1002/alr.70182</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70182</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70182?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70179?af=R</link>
         <pubDate>Wed, 06 May 2026 09:01:33 -0700</pubDate>
         <dc:date>2026-05-06T09:01:33-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70179</guid>
         <title>Dupilumab Alleviates IL‐13‐Induced Nasal Epithelial Barrier Dysfunction by Regulating Claudin‐10 Expression</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Backgrounds
Nasal epithelial barrier impairment is a crucial pathology in chronic rhinosinusitis with nasal polyps (CRSwNP). However, the mechanisms driving tight junctions (TJs) disruption remain unclear. We aimed to elucidate the role of IL‐13 in TJs breakdown and epithelial remodeling, and to evaluate whether dupilumab can restore epithelial integrity under Type‐2 inflammatory conditions.


Methods
Differentially expressed TJs‐related genes were identified by integrating the GSE136825 dataset with clinical samples from 23 healthy controls and 73 CRSwNP patients. The effects of IFN‐γ, IL‐13, IL‐17A, and dupilumab on epithelial barrier function and claudin‐10 (CLDN10) expression were investigated in seven human nasal epithelial cells using transepithelial electrical resistance (TER), RT‐qPCR, WB, and immunofluorescence. Statistical analyses were performed using the chi‐square test, one‐way ANOVA, Wilcoxon signed‐rank test, and Spearman's rank correlation.


Results
CLDN10 was identified as the most significantly downregulated TJs in CRSwNP and negatively correlated with eosinophil infiltration (r = −0.4414, p &lt; 0.0001). In vitro, IL‐13 markedly reduced CLDN10 and TER levels, and induced epithelial remodeling with fewer club cells and ciliated cells and more goblet cells (all p &lt; 0.05). Additionally, dupilumab effectively mitigated IL‐13‐induced CLDN10 loss, restored barrier integrity, and normalized epithelial alarmins, including IL‐25 and TSLP expression (all p &lt; 0.05).


Conclusions
IL‐13‐driven Type‐2 inflammation disrupts nasal epithelial barrier integrity by downregulating CLDN10 and altering epithelial cell differentiation. Dupilumab counteracts these effects by restoring CLDN10 expression and epithelial barrier function, highlighting CLDN10 as a crucial mediator of barrier dysfunction and a potential therapeutic target in CRSwNP.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Backgrounds&lt;/h2&gt;
&lt;p&gt;Nasal epithelial barrier impairment is a crucial pathology in chronic rhinosinusitis with nasal polyps (CRSwNP). However, the mechanisms driving tight junctions (TJs) disruption remain unclear. We aimed to elucidate the role of IL-13 in TJs breakdown and epithelial remodeling, and to evaluate whether dupilumab can restore epithelial integrity under Type-2 inflammatory conditions.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Differentially expressed TJs-related genes were identified by integrating the GSE136825 dataset with clinical samples from 23 healthy controls and 73 CRSwNP patients. The effects of IFN-γ, IL-13, IL-17A, and dupilumab on epithelial barrier function and claudin-10 (CLDN10) expression were investigated in seven human nasal epithelial cells using transepithelial electrical resistance (TER), RT-qPCR, WB, and immunofluorescence. Statistical analyses were performed using the chi-square test, one-way ANOVA, Wilcoxon signed-rank test, and Spearman's rank correlation.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;CLDN10 was identified as the most significantly downregulated TJs in CRSwNP and negatively correlated with eosinophil infiltration (&lt;i&gt;r&lt;/i&gt; = −0.4414, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001). In vitro, IL-13 markedly reduced CLDN10 and TER levels, and induced epithelial remodeling with fewer club cells and ciliated cells and more goblet cells (all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). Additionally, dupilumab effectively mitigated IL-13-induced CLDN10 loss, restored barrier integrity, and normalized epithelial alarmins, including IL-25 and TSLP expression (all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05).&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;IL-13-driven Type-2 inflammation disrupts nasal epithelial barrier integrity by downregulating CLDN10 and altering epithelial cell differentiation. Dupilumab counteracts these effects by restoring CLDN10 expression and epithelial barrier function, highlighting CLDN10 as a crucial mediator of barrier dysfunction and a potential therapeutic target in CRSwNP.&lt;/p&gt;</content:encoded>
         <dc:creator>
Zhi‐Qun Huang, 
Jing Liu, 
Li‐Ying Sun, 
Qing Luo, 
Jie‐Qing Yu, 
Li Shen, 
Yi‐Shan Xiong, 
Ran‐Ran Yin, 
De‐Yun Wang, 
Jing Ye
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Dupilumab Alleviates IL‐13‐Induced Nasal Epithelial Barrier Dysfunction by Regulating Claudin‐10 Expression</dc:title>
         <dc:identifier>10.1002/alr.70179</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70179</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70179?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70176?af=R</link>
         <pubDate>Tue, 05 May 2026 08:00:34 -0700</pubDate>
         <dc:date>2026-05-05T08:00:34-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70176</guid>
         <title>Distribution of Eosinophils Across Multiple Paranasal Sinuses Within Patients With Chronic Rhinosinusitis With Nasal Polyps</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
A single nasal polyp is frequently used for research purposes. We intended to investigate whether a single nasal polyp reflects the total inflammatory load in patients with chronic rhinosinusitis with nasal polyps (CRSwNP).


Methods
We intended to prospectively collect polyps from four sites of 30 subjects during surgery for CRSwNP. We collected the most anterior located polyp and polyps of the posterior ethmoidal area on each side. A pathologist, blinded to the sampling sites, quantified the tissue eosinophilic count in the three most dense high‐power fields with hematoxylin and eosin staining. We investigated the coefficient of variation within subjects and compared differences across the four sites with the Friedman's test. Moreover, we examined how many subjects had more or less than 10 eosinophils across all four sites and could be characterized as eosinophilic‐ or non‐eosinophilic CRSwNP according to recent guidelines.


Results
The mean coefficient of variation was high (82%). The tissue eosinophilic count differed significantly across the four sites when sorted from the lowest to the highest tissue eosinophilic count (Friedman's test; p &lt; 0.001), with significant differences between each rank (Wilcoxon signed‐rank test; all p &lt; 0.001). The median tissue eosinophilic counts across the four different sites, when sorted from the lowest to the highest rank, were 7, 27, 52, and 161 eosinophils. Only 14 of 30 subjects had more or fewer than 10 eosinophils across all sites.


Conclusion
The distribution of eosinophils may differ substantially across the paranasal sinuses. Investigation of a single nasal polyp may not reflect the total inflammatory load.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;A single nasal polyp is frequently used for research purposes. We intended to investigate whether a single nasal polyp reflects the total inflammatory load in patients with chronic rhinosinusitis with nasal polyps (CRSwNP).&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We intended to prospectively collect polyps from four sites of 30 subjects during surgery for CRSwNP. We collected the most anterior located polyp and polyps of the posterior ethmoidal area on each side. A pathologist, blinded to the sampling sites, quantified the tissue eosinophilic count in the three most dense high-power fields with hematoxylin and eosin staining. We investigated the coefficient of variation within subjects and compared differences across the four sites with the Friedman's test. Moreover, we examined how many subjects had more or less than 10 eosinophils across all four sites and could be characterized as eosinophilic- or non-eosinophilic CRSwNP according to recent guidelines.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;The mean coefficient of variation was high (82%). The tissue eosinophilic count differed significantly across the four sites when sorted from the lowest to the highest tissue eosinophilic count (Friedman's test; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), with significant differences between each rank (Wilcoxon signed-rank test; all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001). The median tissue eosinophilic counts across the four different sites, when sorted from the lowest to the highest rank, were 7, 27, 52, and 161 eosinophils. Only 14 of 30 subjects had more or fewer than 10 eosinophils across all sites.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;The distribution of eosinophils may differ substantially across the paranasal sinuses. Investigation of a single nasal polyp may not reflect the total inflammatory load.&lt;/p&gt;</content:encoded>
         <dc:creator>
Aris I. Giotakis, 
Athanasios Ioannidis, 
Efthymios Kyrodimos, 
Efthymios Koniaris, 
Evangelos I. Giotakis, 
Dimitra Riga
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Distribution of Eosinophils Across Multiple Paranasal Sinuses Within Patients With Chronic Rhinosinusitis With Nasal Polyps</dc:title>
         <dc:identifier>10.1002/alr.70176</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70176</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70176?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70163?af=R</link>
         <pubDate>Fri, 17 Apr 2026 04:59:38 -0700</pubDate>
         <dc:date>2026-04-17T04:59:38-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70163</guid>
         <title>Prospective Real‐World Outcomes of Endoscopic Sinus Surgery and Dupilumab in Severe Chronic Rhinosinusitis With Nasal Polyps</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
Chronic rhinosinusitis with nasal polyps (CRSwNP) is a heterogeneous inflammatory disease treated with endoscopic sinus surgery (ESS) or targeted biologic therapy such as dupilumab. Prospective real‐world data guiding treatment decisions remain limited.


Materials and Methods
We conducted a single‐center, prospective, real‐world observational cohort study of adults with severe CRSwNP treated with ESS or dupilumab following structured shared decision‐making. All patients met EPOS diagnostic criteria and were followed for 12 months. Standardized assessments were performed at baseline and every 3 months, including disease‐specific quality of life (SNOT‐22), olfaction (UPSIT‐40), nasal congestion score (NCS), and endoscopic nasal polyp score (NPS). CRS exacerbations were prospectively monitored using biweekly symptom surveys, with endoscopic culture obtained during exacerbations with mucopurulence. Longitudinal outcomes were analyzed using mixed‐effects models, and bacterial exacerbation incidence was evaluated using regression and survival analyses.


Results
Fifty adults completed 12‐month follow‐up (dupilumab, n = 20; ESS, n = 30). Both treatments resulted in significant improvements across patient‐reported and objective outcomes, exceeding minimal clinically important differences. ESS was associated with more rapid early improvement, whereas dupilumab demonstrated more durable improvement in symptoms, olfaction, and nasal congestion. CRS exacerbations and culture‐confirmed bacterial infections occurred less frequently in dupilumab‐treated patients, with lower cumulative bacterial burden and longer infection‐free survival. Staphylococcus aureus was the most common pathogen and more frequent among ESS‐treated patients. Bacterial infection was associated with persistently higher symptom burden and worse longitudinal outcomes.


Conclusions
ESS and dupilumab both provide meaningful benefit in severe CRSwNP, with distinct temporal response patterns. Reduced exacerbations and bacterial infections—particularly S. aureus—were associated with more favorable disease trajectories, underscoring the importance of infection control in individualized treatment selection.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis with nasal polyps (CRSwNP) is a heterogeneous inflammatory disease treated with endoscopic sinus surgery (ESS) or targeted biologic therapy such as dupilumab. Prospective real-world data guiding treatment decisions remain limited.&lt;/p&gt;
&lt;h2&gt;Materials and Methods&lt;/h2&gt;
&lt;p&gt;We conducted a single-center, prospective, real-world observational cohort study of adults with severe CRSwNP treated with ESS or dupilumab following structured shared decision-making. All patients met EPOS diagnostic criteria and were followed for 12 months. Standardized assessments were performed at baseline and every 3 months, including disease-specific quality of life (SNOT-22), olfaction (UPSIT-40), nasal congestion score (NCS), and endoscopic nasal polyp score (NPS). CRS exacerbations were prospectively monitored using biweekly symptom surveys, with endoscopic culture obtained during exacerbations with mucopurulence. Longitudinal outcomes were analyzed using mixed-effects models, and bacterial exacerbation incidence was evaluated using regression and survival analyses.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Fifty adults completed 12-month follow-up (dupilumab, &lt;i&gt;n&lt;/i&gt; = 20; ESS, &lt;i&gt;n &lt;/i&gt;= 30). Both treatments resulted in significant improvements across patient-reported and objective outcomes, exceeding minimal clinically important differences. ESS was associated with more rapid early improvement, whereas dupilumab demonstrated more durable improvement in symptoms, olfaction, and nasal congestion. CRS exacerbations and culture-confirmed bacterial infections occurred less frequently in dupilumab-treated patients, with lower cumulative bacterial burden and longer infection-free survival. &lt;i&gt;Staphylococcus aureus&lt;/i&gt; was the most common pathogen and more frequent among ESS-treated patients. Bacterial infection was associated with persistently higher symptom burden and worse longitudinal outcomes.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;ESS and dupilumab both provide meaningful benefit in severe CRSwNP, with distinct temporal response patterns. Reduced exacerbations and bacterial infections—particularly &lt;i&gt;S. aureus&lt;/i&gt;—were associated with more favorable disease trajectories, underscoring the importance of infection control in individualized treatment selection.&lt;/p&gt;</content:encoded>
         <dc:creator>
Nirushan Narendran, 
Joseph Irish, 
Shireen Samargandy, 
Tara Carr, 
Christopher H. Le, 
Eugene H. Chang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Prospective Real‐World Outcomes of Endoscopic Sinus Surgery and Dupilumab in Severe Chronic Rhinosinusitis With Nasal Polyps</dc:title>
         <dc:identifier>10.1002/alr.70163</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70163</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70163?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70171?af=R</link>
         <pubDate>Fri, 17 Apr 2026 04:57:26 -0700</pubDate>
         <dc:date>2026-04-17T04:57:26-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70171</guid>
         <title>Leptin May Promote Eosinophilic CRSwNP Progression by Enhancing Eosinophil Chemotaxis and Angiogenesis Under a Type 2 Inflammatory Milieu</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis with nasal polyp (CRSwNP) is a heterogeneous Type 2 inflammatory disease characterized by enhanced eosinophilic infiltration. Both innate and adaptive immunity are involved in the onset and progression of CRSwNP. Increased serum leptin levels are associated with various allergic conditions; however, the biological role of leptin in allergic immune cells requires further investigation.


Objective
To investigate the effects of leptin on immune cells, including eosinophils, basophils, and mast cells, in CRSwNP.


Methods
Leptin was used to stimulate eosinophils and eosinophilic cell lines, followed by analyses of gene expression, migration, and angiogenic capacity. Immunometabolic profile of CRSwNP, serum leptin, and galectin‐10 levels were analyzed in conjunction with the gene expression profiles of nasal polyps. Furthermore, the biological effects of leptin on eosinophils were assessed using RNA sequencing and functional analyses, including a transwell migration assay and an angiogenesis assay via co‐culture with human umbilical vein endothelial cells (HUVEC).


Results
Increased serum leptin and galectin‐10 levels were associated with Type 2 inflammatory markers and correlated with CRSwNP severity. RNA sequencing revealed upregulation of chemokine ligands in eosinophilic cell lines. Leptin induced plasminogen activator inhibitor 1 (PAI‐1) expression in eosinophils but not in basophils or neutrophils. Leptin pretreatment substantially enhanced migration toward both C–C motif chemokine ligand (CCL) 11 and CCL26 in eosinophilic cell lines. The leptin‐primed eosinophilic cell line promoted angiogenesis, as demonstrated in co‐culture with HUVECs.


Conclusion
Leptin promotes eosinophil migration and angiogenesis, potentially via chemokine ligands and PAI‐1 induction, and may promote CRSwNP progression under a Type 2 inflammatory milieu.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis with nasal polyp (CRSwNP) is a heterogeneous Type 2 inflammatory disease characterized by enhanced eosinophilic infiltration. Both innate and adaptive immunity are involved in the onset and progression of CRSwNP. Increased serum leptin levels are associated with various allergic conditions; however, the biological role of leptin in allergic immune cells requires further investigation.&lt;/p&gt;
&lt;h2&gt;Objective&lt;/h2&gt;
&lt;p&gt;To investigate the effects of leptin on immune cells, including eosinophils, basophils, and mast cells, in CRSwNP.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Leptin was used to stimulate eosinophils and eosinophilic cell lines, followed by analyses of gene expression, migration, and angiogenic capacity. Immunometabolic profile of CRSwNP, serum leptin, and galectin-10 levels were analyzed in conjunction with the gene expression profiles of nasal polyps. Furthermore, the biological effects of leptin on eosinophils were assessed using RNA sequencing and functional analyses, including a transwell migration assay and an angiogenesis assay via co-culture with human umbilical vein endothelial cells (HUVEC).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Increased serum leptin and galectin-10 levels were associated with Type 2 inflammatory markers and correlated with CRSwNP severity. RNA sequencing revealed upregulation of chemokine ligands in eosinophilic cell lines. Leptin induced plasminogen activator inhibitor 1 (PAI-1) expression in eosinophils but not in basophils or neutrophils. Leptin pretreatment substantially enhanced migration toward both C–C motif chemokine ligand (CCL) 11 and CCL26 in eosinophilic cell lines. The leptin-primed eosinophilic cell line promoted angiogenesis, as demonstrated in co-culture with HUVECs.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Leptin promotes eosinophil migration and angiogenesis, potentially via chemokine ligands and PAI-1 induction, and may promote CRSwNP progression under a Type 2 inflammatory milieu.&lt;/p&gt;</content:encoded>
         <dc:creator>
Yuki Sonoda, 
Yohei Sato, 
Yoshimasa Imoto, 
Mayumi Tamari, 
Shigeharu Fujieda
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Leptin May Promote Eosinophilic CRSwNP Progression by Enhancing Eosinophil Chemotaxis and Angiogenesis Under a Type 2 Inflammatory Milieu</dc:title>
         <dc:identifier>10.1002/alr.70171</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70171</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70171?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70165?af=R</link>
         <pubDate>Tue, 14 Apr 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-04-14T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70165</guid>
         <title>Temperature‐Controlled Radiofrequency for Severe Nasal Airway Obstruction: A Non‐Inferiority Comparison With Surgical Intervention</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
Temperature‐controlled radiofrequency (TCRF), septoplasty (ST) with turbinate reduction, and functional rhinoplasty (FR) are treatment options for nasal airway obstruction (NAO) and nasal valve dysfunction (NVD), but no direct comparison of these procedures has been performed.


Methods
This prospective, open‐label, non‐inferiority (NI) trial, conducted at 29 US sites, used a prespecified NI margin and inverse probability of treatment weighting to simulate randomization and facilitate an unbiased comparison of TCRF to ST and FR in adults with Nasal Obstruction Symptom Evaluation scores ≥ 55 and NVD. NI was determined using a 15% difference in the 3‐month responder rate (≥ 24‐point NOSE score improvement) for TCRF compared to ST and FR. Additional analyses included return to work/regular activities (RTW) and adverse events (AEs).


Results
A total of 174 patients were treated (116 TCRF and 58 surgery [35 ST, 23 FR]). At 3 months, TCRF was non‐inferior to surgery with a 90.5% responder rate compared to 94.3% for ST (mean difference: 0.04 [95% CI, −0.02 to 0.11]; p &lt; 0.001) and 95.7% for FR (mean difference: −0.12 [95% CI, −0.23 to 0]; p &lt; 0.001). TCRF median RTW was 1 day versus 5.5 and 7.5 days for ST and FR, respectively. TCRF had fewer AEs than surgery (6.9% TCRF patients vs. 19.0% for surgical arms combined).


Conclusions
TCRF patient treatment response was non‐inferior to ST and FR, with fewer AEs and faster RTW. These findings support TCRF as a minimally invasive alternative to nasal surgery for patients with NAO and NVD.


Trial Registration
ClinicalTrials.gov identifier: NCT06922955

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;Temperature-controlled radiofrequency (TCRF), septoplasty (ST) with turbinate reduction, and functional rhinoplasty (FR) are treatment options for nasal airway obstruction (NAO) and nasal valve dysfunction (NVD), but no direct comparison of these procedures has been performed.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This prospective, open-label, non-inferiority (NI) trial, conducted at 29 US sites, used a prespecified NI margin and inverse probability of treatment weighting to simulate randomization and facilitate an unbiased comparison of TCRF to ST and FR in adults with Nasal Obstruction Symptom Evaluation scores ≥ 55 and NVD. NI was determined using a 15% difference in the 3-month responder rate (≥ 24-point NOSE score improvement) for TCRF compared to ST and FR. Additional analyses included return to work/regular activities (RTW) and adverse events (AEs).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;A total of 174 patients were treated (116 TCRF and 58 surgery [35 ST, 23 FR]). At 3 months, TCRF was non-inferior to surgery with a 90.5% responder rate compared to 94.3% for ST (mean difference: 0.04 [95% CI, −0.02 to 0.11]; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001) and 95.7% for FR (mean difference: −0.12 [95% CI, −0.23 to 0]; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001). TCRF median RTW was 1 day versus 5.5 and 7.5 days for ST and FR, respectively. TCRF had fewer AEs than surgery (6.9% TCRF patients vs. 19.0% for surgical arms combined).&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;TCRF patient treatment response was non-inferior to ST and FR, with fewer AEs and faster RTW. These findings support TCRF as a minimally invasive alternative to nasal surgery for patients with NAO and NVD.&lt;/p&gt;
&lt;h2&gt;Trial Registration&lt;/h2&gt;
&lt;p&gt;ClinicalTrials.gov identifier: NCT06922955&lt;/p&gt;</content:encoded>
         <dc:creator>
Greg Davis, 
Zeeshan Aziz, 
Jose Barrera, 
William Blythe, 
Chris Davis, 
Steven Davis, 
Thomas Higgins, 
Charles Lano, 
Gregory Levitin, 
Frederick Lopatin, 
Samuel Oyer, 
Stacey Silvers, 
Ariel Waitzman, 
Randall Ow
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Temperature‐Controlled Radiofrequency for Severe Nasal Airway Obstruction: A Non‐Inferiority Comparison With Surgical Intervention</dc:title>
         <dc:identifier>10.1002/alr.70165</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70165</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70165?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70166?af=R</link>
         <pubDate>Fri, 10 Apr 2026 08:05:08 -0700</pubDate>
         <dc:date>2026-04-10T08:05:08-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70166</guid>
         <title>Extent of Sinus Surgery Is Associated With Disease Control in Biologic Treated Type 2 Dominant CRS</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
A greater benefit of biologics is observed after surgery in Type 2 chronic rhinosinusitis with nasal polyps (CRSwNP). However, the extent of surgery remains undefined in many studies. This study evaluated the extent of surgery on disease control in patients receiving biologics for refractory Type 2 dominant CRSwNP.


Methods
A cross‐sectional study was performed on patients with CRSwNP treated with biologics for ≥ 6 months at a tertiary center. All patients had undergone prior sinus surgery, which included a sphenoethmoidectomy and then extension via Draf I, IIa, IIb, IIc, or III. Disease control was defined as having a SNOT‐22 ≤ 30, endoscopic modified Lund–Mackay ≤ 4, and the absence of rescue therapy within 6 months. Comparisons were made across surgical and biologic groups, and logistic regression was used to identify factors associated with disease control.


Results
A total of 159 patients were assessed (age 50.9 ± 12.8 years, 45.3% female). Disease control was achieved in 49.1% of patients. Disease control was greater with extended surgery (Draf III 60.8% [49.7%–70.8%] vs. Draf IIc 68.3% [53.0%–80.4%] vs. Draf IIa 8.7% [2.4%–26.8%] vs. Draf I 0% [0.0%–19.4%]; p &lt; 0.001). The control was similar across biologic types (anti‐IL‐4αR 63.3% [45.5%–78.1%] vs. anti‐IL‐5/5R 45.7% [37.3%–54.3%]; p = 0.083). On regression, extended surgery (Draf III + IIc) was associated with disease control (Draf III/IIc vs. Draf IIa/I OR: 110.2 [12.7–14,682.5]) but not biologic type (anti‐IL‐4αR vs. anti‐IL‐5/5R OR: 2.2 [0.7–7.2]). However, class switching had already occurred in 15.1% of patients initially treated with anti‐IL‐5/5R.


Conclusions
Disease control was greatest in CRSwNP patients who had both extended sinus surgery and optimized biologic treatment.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;A greater benefit of biologics is observed after surgery in Type 2 chronic rhinosinusitis with nasal polyps (CRSwNP). However, the extent of surgery remains undefined in many studies. This study evaluated the extent of surgery on disease control in patients receiving biologics for refractory Type 2 dominant CRSwNP.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A cross-sectional study was performed on patients with CRSwNP treated with biologics for ≥ 6 months at a tertiary center. All patients had undergone prior sinus surgery, which included a sphenoethmoidectomy and then extension via Draf I, IIa, IIb, IIc, or III. Disease control was defined as having a SNOT-22 ≤ 30, endoscopic modified Lund–Mackay ≤ 4, and the absence of rescue therapy within 6 months. Comparisons were made across surgical and biologic groups, and logistic regression was used to identify factors associated with disease control.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;A total of 159 patients were assessed (age 50.9 ± 12.8 years, 45.3% female). Disease control was achieved in 49.1% of patients. Disease control was greater with extended surgery (Draf III 60.8% [49.7%–70.8%] vs. Draf IIc 68.3% [53.0%–80.4%] vs. Draf IIa 8.7% [2.4%–26.8%] vs. Draf I 0% [0.0%–19.4%]; &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001). The control was similar across biologic types (anti-IL-4αR 63.3% [45.5%–78.1%] vs. anti-IL-5/5R 45.7% [37.3%–54.3%]; &lt;i&gt;p&lt;/i&gt; = 0.083). On regression, extended surgery (Draf III + IIc) was associated with disease control (Draf III/IIc vs. Draf IIa/I OR: 110.2 [12.7–14,682.5]) but not biologic type (anti-IL-4αR vs. anti-IL-5/5R OR: 2.2 [0.7–7.2]). However, class switching had already occurred in 15.1% of patients initially treated with anti-IL-5/5R.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Disease control was greatest in CRSwNP patients who had both extended sinus surgery and optimized biologic treatment.&lt;/p&gt;</content:encoded>
         <dc:creator>
Nicholas J. Campion, 
Peta‐Lee Sacks, 
Lu Hui Png, 
Ruoxin Hua, 
Rhea Darbari Kaul, 
Raquel Alvarado, 
Christine Choy, 
Raymond Sacks, 
Peter Earls, 
Raewyn G. Campbell, 
Larry Kalish, 
Richard J. Harvey
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Extent of Sinus Surgery Is Associated With Disease Control in Biologic Treated Type 2 Dominant CRS</dc:title>
         <dc:identifier>10.1002/alr.70166</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70166</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70166?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70147?af=R</link>
         <pubDate>Fri, 03 Apr 2026 05:34:22 -0700</pubDate>
         <dc:date>2026-04-03T05:34:22-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70147</guid>
         <title>Oral Steroid Use and Asthma Comorbidity in Central Compartment Atopic Disease: The Predictive Role of Olfactory Dysfunction and Eosinophilia</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Central compartment atopic disease (CCAD) is a distinct phenotype of chronic rhinosinusitis with nasal polyps (CRSwNP), characterized by central nasal cavity inflammation. Although well described in Western populations, data from East Asia remain limited. We aimed to characterize CCAD's clinical features, identify predictors of postoperative oral corticosteroid (OCS) use, and explore CCAD's association with comorbid asthma.


Methods
In this propensity score‐matched case‐control study, patients with bilateral CRSwNP were classified as CCAD or non‐CCAD using endoscopic findings. Clinical characteristics, laboratory markers, and surgical outcomes were compared. Subgroup analysis within CCAD evaluated predictors of postoperative OCS use and comorbid asthma.


Results
Compared with non‐CCAD CRSwNP, CCAD patients had more severe subjective olfactory dysfunction (p = 0.035) and a distinct allergic inflammatory profile, including higher blood and tissue eosinophils, serum immunoglobulin E, and eosinophil cationic protein. Within the CCAD cohort, patients requiring postoperative OCS use had greater tissue eosinophilia; a threshold of ≥ 21 cells/high‐power field independently predicted OCS need (hazard ratio = 12.4, 95% confidence interval = 1.6–93.4, p = 0.015). Comorbid asthma was associated with higher Lund–Mackay scores and blood eosinophilia (p = 0.012 and p = 0.007, respectively).


Conclusions
CCAD is associated with greater subjective olfactory dysfunction and a distinct allergic inflammatory profile. Tissue eosinophilia independently predicts postoperative corticosteroid use, while advanced disease and elevated blood eosinophils predict comorbid asthma. These findings support risk stratification and personalized postoperative management in CCAD.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Central compartment atopic disease (CCAD) is a distinct phenotype of chronic rhinosinusitis with nasal polyps (CRSwNP), characterized by central nasal cavity inflammation. Although well described in Western populations, data from East Asia remain limited. We aimed to characterize CCAD's clinical features, identify predictors of postoperative oral corticosteroid (OCS) use, and explore CCAD's association with comorbid asthma.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;In this propensity score-matched case-control study, patients with bilateral CRSwNP were classified as CCAD or non-CCAD using endoscopic findings. Clinical characteristics, laboratory markers, and surgical outcomes were compared. Subgroup analysis within CCAD evaluated predictors of postoperative OCS use and comorbid asthma.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Compared with non-CCAD CRSwNP, CCAD patients had more severe subjective olfactory dysfunction (&lt;i&gt;p&lt;/i&gt; = 0.035) and a distinct allergic inflammatory profile, including higher blood and tissue eosinophils, serum immunoglobulin E, and eosinophil cationic protein. Within the CCAD cohort, patients requiring postoperative OCS use had greater tissue eosinophilia; a threshold of ≥ 21 cells/high-power field independently predicted OCS need (hazard ratio = 12.4, 95% confidence interval = 1.6–93.4, &lt;i&gt;p&lt;/i&gt; = 0.015). Comorbid asthma was associated with higher Lund–Mackay scores and blood eosinophilia (&lt;i&gt;p&lt;/i&gt; = 0.012 and &lt;i&gt;p&lt;/i&gt; = 0.007, respectively).&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;CCAD is associated with greater subjective olfactory dysfunction and a distinct allergic inflammatory profile. Tissue eosinophilia independently predicts postoperative corticosteroid use, while advanced disease and elevated blood eosinophils predict comorbid asthma. These findings support risk stratification and personalized postoperative management in CCAD.&lt;/p&gt;</content:encoded>
         <dc:creator>
Lin Hsu, 
Chia‐Chen Wu, 
Hsiang‐Sheng Wang, 
Chien‐Cheng Chen, 
Ta‐Jen Lee, 
Po‐Hung Chang, 
Yi‐Wei Chen, 
Yu‐Ning Tsao, 
Hsiang‐An Hsueh, 
Ya‐Cheng Tang, 
Chia‐Hsiang Fu
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Oral Steroid Use and Asthma Comorbidity in Central Compartment Atopic Disease: The Predictive Role of Olfactory Dysfunction and Eosinophilia</dc:title>
         <dc:identifier>10.1002/alr.70147</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70147</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70147?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70146?af=R</link>
         <pubDate>Tue, 31 Mar 2026 07:48:54 -0700</pubDate>
         <dc:date>2026-03-31T07:48:54-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70146</guid>
         <title>Biofilm Exoproteins From Staphylococcus Species Impede Re‐Epithelialization of Nasal Epithelial Cells During Wound Healing and Cease Ciliary Beat Frequency</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
Chronic rhinosinusitis (CRS) is an inflammatory disease with many different contributing factors, including bacterial infection. CRS patients are typically managed with medical therapies; however, these treatments frequently fail, leaving surgery as the only viable option. Despite surgical intervention, patients may experience ongoing clinical manifestations of inflammation and infection, frequently associated with Staphylococcus species colonization. This study explored the influence of Staphylococcus on the wound healing process and ciliary function in vitro.


Methods
Exoproteins were extracted from biofilm forms of 15 Staphylococcus isolates obtained from five patients (4 CRS and 1 control patient), each colonized by Staphylococcus aureus, Staphylococcus epidermidis, and Staphylococcus lugdunensis. Human nasal epithelial cells (HNECs) were cultured in monolayers for wound healing assays and at an air–liquid interface (ALI) for ciliary beat frequency measurements. Wound closure, cytotoxicity, interleukin‐6 (IL‐6), and reactive oxygen species (ROS) release were measured after 30 h post‐wound creation.


Results
Biofilm exoproteins from all three Staphylococcus species hindered the re‐epithelialization of HNECs at 5 and 10 µg/mL with S. aureus exoproteins having significantly stronger effects on impairing wound closure compared to S. lugdunensis exoproteins. S. aureus exerted the most pronounced cytotoxic effect compared to the control. Furthermore, all Staphylococcus species reduced ROS release by HNECs while S. epidermidis and S. lugdunensis induced higher IL‐6 levels compared to control. In HNEC‐ALI cultures, ciliary beat frequency was significantly reduced by all staphylococci 5 h after application of exoproteins.


Conclusion
Staphylococcal biofilm exoproteins hindered mucociliary function and re‐epithelialization of the nasal epithelium, caused cytotoxicity, elicited inflammation, and concurrently reduced ROS release.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis (CRS) is an inflammatory disease with many different contributing factors, including bacterial infection. CRS patients are typically managed with medical therapies; however, these treatments frequently fail, leaving surgery as the only viable option. Despite surgical intervention, patients may experience ongoing clinical manifestations of inflammation and infection, frequently associated with &lt;i&gt;Staphylococcus&lt;/i&gt; species colonization. This study explored the influence of &lt;i&gt;Staphylococcus&lt;/i&gt; on the wound healing process and ciliary function in vitro.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Exoproteins were extracted from biofilm forms of 15 &lt;i&gt;Staphylococcus&lt;/i&gt; isolates obtained from five patients (4 CRS and 1 control patient), each colonized by &lt;i&gt;Staphylococcus aureus, Staphylococcus epidermidis&lt;/i&gt;, and &lt;i&gt;Staphylococcus lugdunensis&lt;/i&gt;. Human nasal epithelial cells (HNECs) were cultured in monolayers for wound healing assays and at an air–liquid interface (ALI) for ciliary beat frequency measurements. Wound closure, cytotoxicity, interleukin-6 (IL-6), and reactive oxygen species (ROS) release were measured after 30 h post-wound creation.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Biofilm exoproteins from all three &lt;i&gt;Staphylococcus&lt;/i&gt; species hindered the re-epithelialization of HNECs at 5 and 10 µg/mL with &lt;i&gt;S. aureus&lt;/i&gt; exoproteins having significantly stronger effects on impairing wound closure compared to &lt;i&gt;S. lugdunensis&lt;/i&gt; exoproteins. &lt;i&gt;S. aureus&lt;/i&gt; exerted the most pronounced cytotoxic effect compared to the control. Furthermore, all &lt;i&gt;Staphylococcus&lt;/i&gt; species reduced ROS release by HNECs while &lt;i&gt;S. epidermidis&lt;/i&gt; and &lt;i&gt;S. lugdunensis&lt;/i&gt; induced higher IL-6 levels compared to control. In HNEC-ALI cultures, ciliary beat frequency was significantly reduced by all staphylococci 5 h after application of exoproteins.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Staphylococcal biofilm exoproteins hindered mucociliary function and re-epithelialization of the nasal epithelium, caused cytotoxicity, elicited inflammation, and concurrently reduced ROS release.&lt;/p&gt;</content:encoded>
         <dc:creator>
Sintayehu Ambachew, 
Mahnaz Ramezanpour, 
Clare M. Cooksley, 
Emma F. Barry, 
Lindsay Durr, 
Kevin Aaron Fenix, 
P. J. Wormald, 
Alkis J. Psaltis, 
Sarah Vreugde
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Biofilm Exoproteins From Staphylococcus Species Impede Re‐Epithelialization of Nasal Epithelial Cells During Wound Healing and Cease Ciliary Beat Frequency</dc:title>
         <dc:identifier>10.1002/alr.70146</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70146</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70146?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70148?af=R</link>
         <pubDate>Tue, 31 Mar 2026 07:45:45 -0700</pubDate>
         <dc:date>2026-03-31T07:45:45-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70148</guid>
         <title>Interspecies Biofilm Dynamics Among Staphylococci: Inflammatory Contributions to Chronic Rhinosinusitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
Staphylococcus species are frequently isolated from the sinonasal niche of chronic rhinosinusitis (CRS) patients. While Staphylococcus aureus is often associated with recalcitrant CRS, Staphylococcus epidermidis and Staphylococcus lugdunensis are largely deemed commensal. The purpose of this study was to investigate interspecies interactions and how those might influence inflammation and susceptibility to antibiotics.


Methods
Twelve staphylococcal isolates were harvested from six CRS patients, each infected with S. aureus and S. epidermidis, or with S. aureus and S. lugdunensis. Bacteria were cultured to allow biofilm formation in direct and indirect interspecies interactions, followed by measuring their biofilm biomass, antibiotic sensitivity, and toxicity and inflammatory potential when applied to human nasal epithelial cells (HNECs).


Results
S. epidermidis produced up to 7.4‐fold higher biomass than S. aureus in monocultures, with a reduction in S. epidermidis biomass under indirect coculture conditions with S. aureus biofilm (p &lt; 0.05). In contrast, the biofilm biomass values of both S. lugdunensis and S. aureus were higher under indirect coculture conditions compared to monocultures for 2/3 paired isolates (p &lt; 0.05). S. epidermidis monocultures and S. aureus/S. epidermidis cocultures were less toxic to HNECs than S. aureus monocultures. S. aureus and S. lugdunensis monocultures and S. aureus/S. lugdunensis cocultures induced interleukin‐6 (IL‐6) and toxicity to a similar extent versus controls. An increased tolerance to amoxicillin was observed for 2/3 S. epidermidis biofilm and for 3/3 S. lugdunensis biofilm when in indirect contact with S. aureus biofilm (p &lt; 0.05).


Conclusion
Overall, staphylococcal interactions were highly strain specific, with S. aureus influencing the biofilm‐forming capacity and increasing the tolerance to amoxicillin of both S. epidermidis and S. lugdunensis. S. epidermidis but not S. lugdunensis could mitigate S. aureus induced epithelial cytotoxicity. These findings support the complex nature of interactions among staphylococci with S. aureus and potentially S. lugdunensis having a pathogenic role and S. epidermidis a protective role within polymicrobial biofilms. Our findings have implications for the inflammatory potential and response to therapy of mixed biofilms.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;&lt;i&gt;Staphylococcus&lt;/i&gt; species are frequently isolated from the sinonasal niche of chronic rhinosinusitis (CRS) patients. While &lt;i&gt;Staphylococcus aureus&lt;/i&gt; is often associated with recalcitrant CRS, &lt;i&gt;Staphylococcus epidermidis&lt;/i&gt; and &lt;i&gt;Staphylococcus lugdunensis&lt;/i&gt; are largely deemed commensal. The purpose of this study was to investigate interspecies interactions and how those might influence inflammation and susceptibility to antibiotics.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Twelve staphylococcal isolates were harvested from six CRS patients, each infected with &lt;i&gt;S. aureus&lt;/i&gt; and &lt;i&gt;S. epidermidis&lt;/i&gt;, or with &lt;i&gt;S. aureus&lt;/i&gt; and &lt;i&gt;S. lugdunensis&lt;/i&gt;. Bacteria were cultured to allow biofilm formation in direct and indirect interspecies interactions, followed by measuring their biofilm biomass, antibiotic sensitivity, and toxicity and inflammatory potential when applied to human nasal epithelial cells (HNECs).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;&lt;i&gt;S. epidermidis&lt;/i&gt; produced up to 7.4-fold higher biomass than &lt;i&gt;S. aureus&lt;/i&gt; in monocultures, with a reduction in &lt;i&gt;S. epidermidis&lt;/i&gt; biomass under indirect coculture conditions with &lt;i&gt;S. aureus&lt;/i&gt; biofilm (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). In contrast, the biofilm biomass values of both &lt;i&gt;S. lugdunensis&lt;/i&gt; and &lt;i&gt;S. aureus&lt;/i&gt; were higher under indirect coculture conditions compared to monocultures for 2/3 paired isolates (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). &lt;i&gt;S. epidermidis&lt;/i&gt; monocultures and &lt;i&gt;S. aureus&lt;/i&gt;/&lt;i&gt;S. epidermidis&lt;/i&gt; cocultures were less toxic to HNECs than &lt;i&gt;S. aureus&lt;/i&gt; monocultures. &lt;i&gt;S. aureus&lt;/i&gt; and &lt;i&gt;S. lugdunensis&lt;/i&gt; monocultures and &lt;i&gt;S. aureus/S. lugdunensis&lt;/i&gt; cocultures induced interleukin-6 (IL-6) and toxicity to a similar extent versus controls. An increased tolerance to amoxicillin was observed for 2/3 &lt;i&gt;S. epidermidis&lt;/i&gt; biofilm and for 3/3 &lt;i&gt;S. lugdunensis&lt;/i&gt; biofilm when in indirect contact with &lt;i&gt;S. aureus&lt;/i&gt; biofilm (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Overall, staphylococcal interactions were highly strain specific, with &lt;i&gt;S. aureus&lt;/i&gt; influencing the biofilm-forming capacity and increasing the tolerance to amoxicillin of both &lt;i&gt;S. epidermidis&lt;/i&gt; and &lt;i&gt;S. lugdunensis&lt;/i&gt;. &lt;i&gt;S. epidermidis&lt;/i&gt; but not &lt;i&gt;S. lugdunensis&lt;/i&gt; could mitigate &lt;i&gt;S. aureus&lt;/i&gt; induced epithelial cytotoxicity. These findings support the complex nature of interactions among staphylococci with &lt;i&gt;S. aureus&lt;/i&gt; and potentially &lt;i&gt;S. lugdunensis&lt;/i&gt; having a pathogenic role and &lt;i&gt;S. epidermidis&lt;/i&gt; a protective role within polymicrobial biofilms. Our findings have implications for the inflammatory potential and response to therapy of mixed biofilms.&lt;/p&gt;</content:encoded>
         <dc:creator>
Sintayehu Ambachew, 
Mahnaz Ramezanpour, 
Clare M. Cooksley, 
Sholeh Feizi, 
Muhammed Awad, 
Kevin Aaron Fenix, 
Peter‐John Wormald, 
Alkis J. Psaltis, 
Sarah Vreugde
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Interspecies Biofilm Dynamics Among Staphylococci: Inflammatory Contributions to Chronic Rhinosinusitis</dc:title>
         <dc:identifier>10.1002/alr.70148</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70148</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70148?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70149?af=R</link>
         <pubDate>Tue, 31 Mar 2026 07:44:41 -0700</pubDate>
         <dc:date>2026-03-31T07:44:41-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70149</guid>
         <title>Recovery of Parosmia Preferentially Influences Longitudinal Improvement of Quality of Life in C19OD</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Persistent COVID‐associated olfactory dysfunction (C19OD) negatively impacts quality of life (QoL). This prospective longitudinal cohort study sought to determine which aspects of chemosensory recovery may preferentially influence QoL improvement in this population.


Methods
Individuals with C19OD (N = 100) completed chemosensory and QoL assessment with Sniffin’ Sticks, Taste Assessment, Questionnaire of Olfactory Disorders‐Negative Statements (QOD‐NS), and QOD‐PAR at baseline and 1 year. Multivariable analyses assessed baseline and longitudinal associations between chemosensory dysfunction and QOD‐NS.


Results
QoL associated with TDI (Coef.; [CI]; p‐value: −0.32; [−0.62, −0.032]; 0.030), threshold (−0.82; [−1.5, −0.14]; 0.019), QOD‐Par (−1.0; [−0.20, −1.9]; 0.016), and self‐reported gustatory dysfunction (GD) (−7.4; [−14, −0.46]; 0.037) at baseline assessment, though quantitative GD did not associate with QoL. Longitudinally, improvements in discrimination (−1.2; [−2.3, −0.18]; 0.023) and QOD‐Par (−2.5; [−0.99, −4.1]; 0.002) scores were associated with improved QoL. Individuals with improved parosmia symptoms experienced a 12.86 (12.99, 0.040) QOD‐NS point improvement from baseline compared to 5.91 (7.98, &lt; 0.001) for those with persistent parosmia.


Conclusions
Independent of mental health, chemosensory function independently drives QoL in C19OD. Parosmia, low odor threshold, and patient‐reported GD are all associated with poorer QoL at baseline. Longitudinally, the ability to differentiate among odors is an important correlate of improvement of smell‐related QoL in C19OD patients, while parosmia is the strongest driver of longitudinal recovery of smell‐related QoL in C19OD. Trending domain‐specific olfactory performance in C19OD may allow for improved patient counseling and QoL prognosis.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Persistent COVID-associated olfactory dysfunction (C19OD) negatively impacts quality of life (QoL). This prospective longitudinal cohort study sought to determine which aspects of chemosensory recovery may preferentially influence QoL improvement in this population.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Individuals with C19OD (&lt;i&gt;N&lt;/i&gt; = 100) completed chemosensory and QoL assessment with Sniffin’ Sticks, Taste Assessment, Questionnaire of Olfactory Disorders-Negative Statements (QOD-NS), and QOD-PAR at baseline and 1 year. Multivariable analyses assessed baseline and longitudinal associations between chemosensory dysfunction and QOD-NS.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;QoL associated with TDI (Coef.; [CI]; &lt;i&gt;p&lt;/i&gt;-value: −0.32; [−0.62, −0.032]; 0.030), threshold (−0.82; [−1.5, −0.14]; 0.019), QOD-Par (−1.0; [−0.20, −1.9]; 0.016), and self-reported gustatory dysfunction (GD) (−7.4; [−14, −0.46]; 0.037) at baseline assessment, though quantitative GD did not associate with QoL. Longitudinally, improvements in discrimination (−1.2; [−2.3, −0.18]; 0.023) and QOD-Par (−2.5; [−0.99, −4.1]; 0.002) scores were associated with improved QoL. Individuals with improved parosmia symptoms experienced a 12.86 (12.99, 0.040) QOD-NS point improvement from baseline compared to 5.91 (7.98, &amp;lt; 0.001) for those with persistent parosmia.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Independent of mental health, chemosensory function independently drives QoL in C19OD. Parosmia, low odor threshold, and patient-reported GD are all associated with poorer QoL at baseline. Longitudinally, the ability to differentiate among odors is an important correlate of improvement of smell-related QoL in C19OD patients, while parosmia is the strongest driver of longitudinal recovery of smell-related QoL in C19OD. Trending domain-specific olfactory performance in C19OD may allow for improved patient counseling and QoL prognosis.&lt;/p&gt;</content:encoded>
         <dc:creator>
Tiana M. Saak, 
Jeremy P. Tervo, 
Brandon J. Vilarello, 
Patricia T. Jacobson, 
Francesco F. Caruana, 
Liam W. Gallagher, 
David A. Gudis, 
Davangere P. Devanand, 
Jonathan B. Overdevest
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Recovery of Parosmia Preferentially Influences Longitudinal Improvement of Quality of Life in C19OD</dc:title>
         <dc:identifier>10.1002/alr.70149</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70149</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70149?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70141?af=R</link>
         <pubDate>Fri, 13 Mar 2026 23:29:40 -0700</pubDate>
         <dc:date>2026-03-13T11:29:40-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70141</guid>
         <title>Allergic Rhinitis Amplifies Asthma Risk in Patients With Chronic Rhinosinusitis: A Large‐Scale Retrospective Cohort Analysis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis (CRS) and allergic rhinitis (AR) are two highly prevalent airway diseases in the United States. While the coexistence of CRS and asthma is well recognized, less is known about the development of new‐onset asthma in CRS, particularly in the context of comorbid AR. This study assessed the impact of CRS and AR on incident asthma using a large electronic health record (EHR) database.


Methods
We conducted a retrospective cohort study using the TriNetX US Collaborative Network, a federated EHR platform encompassing over 100 million patients. Adults ≥ 18 years between January 2009 and December 2019 with CRS were compared to controls without CRS. A second analysis compared patients with CRS and concurrent AR to those with CRS alone. Supplemental analyses substituted chronic rhinosinusitis with nasal polyps (CRSwNP) for CRS. Propensity score matching balanced cohorts on demographics and comorbidities. Primary outcomes were new‐onset asthma and asthma exacerbations, assessed at 1, 2, and 5 years.


Results
After matching, pre‐existing CRS was associated with higher risk of new‐onset asthma (adjusted relative risk [aRR] = 1.42, 95% CI 1.36–1.48) and exacerbations (aRR = 1.87, 95% CI 1.75–2.00) at 1 year versus CRS controls, with similar trends at 2 and 5 years. Coexisting AR further amplified risk: patients with CRS + AR had increased asthma incidence relative to CRS alone at 1 year (aRR = 1.69, 95% CI 1.65–1.73), 2 years (aRR = 1.65, 95% CI 1.62–1.68), and 5 years (aRR = 1.58, 95% CI 1.56–1.60), with more than doubled exacerbation risk across all time points. Directionally similar findings were observed in CRSwNP analyses.


Conclusions
CRS is associated with increased risk of incident asthma and subsequent exacerbations, and coexisting AR identifies a higher‐risk phenotype within CRS. These findings highlight the need for phenotype‐informed studies to determine whether targeted upper‐airway management can mitigate downstream asthma burden.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis (CRS) and allergic rhinitis (AR) are two highly prevalent airway diseases in the United States. While the coexistence of CRS and asthma is well recognized, less is known about the development of new-onset asthma in CRS, particularly in the context of comorbid AR. This study assessed the impact of CRS and AR on incident asthma using a large electronic health record (EHR) database.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We conducted a retrospective cohort study using the TriNetX US Collaborative Network, a federated EHR platform encompassing over 100 million patients. Adults ≥ 18 years between January 2009 and December 2019 with CRS were compared to controls without CRS. A second analysis compared patients with CRS and concurrent AR to those with CRS alone. Supplemental analyses substituted chronic rhinosinusitis with nasal polyps (CRSwNP) for CRS. Propensity score matching balanced cohorts on demographics and comorbidities. Primary outcomes were new-onset asthma and asthma exacerbations, assessed at 1, 2, and 5 years.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;After matching, pre-existing CRS was associated with higher risk of new-onset asthma (adjusted relative risk [aRR] = 1.42, 95% CI 1.36–1.48) and exacerbations (aRR = 1.87, 95% CI 1.75–2.00) at 1 year versus CRS controls, with similar trends at 2 and 5 years. Coexisting AR further amplified risk: patients with CRS + AR had increased asthma incidence relative to CRS alone at 1 year (aRR = 1.69, 95% CI 1.65–1.73), 2 years (aRR = 1.65, 95% CI 1.62–1.68), and 5 years (aRR = 1.58, 95% CI 1.56–1.60), with more than doubled exacerbation risk across all time points. Directionally similar findings were observed in CRSwNP analyses.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;CRS is associated with increased risk of incident asthma and subsequent exacerbations, and coexisting AR identifies a higher-risk phenotype within CRS. These findings highlight the need for phenotype-informed studies to determine whether targeted upper-airway management can mitigate downstream asthma burden.&lt;/p&gt;</content:encoded>
         <dc:creator>
Austin J. Lee, 
Mohamad R. Chaaban
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Allergic Rhinitis Amplifies Asthma Risk in Patients With Chronic Rhinosinusitis: A Large‐Scale Retrospective Cohort Analysis</dc:title>
         <dc:identifier>10.1002/alr.70141</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70141</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70141?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70136?af=R</link>
         <pubDate>Fri, 13 Mar 2026 00:00:00 -0700</pubDate>
         <dc:date>2026-03-13T12:00:00-07:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70136</guid>
         <title>Determining the Minimal Clinically Important Difference of the 40‐Item Smell Identification Test in People With Cystic Fibrosis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis (CRS) and olfactory dysfunction (OD) are highly prevalent among people with cystic fibrosis (PwCF) and negatively impact quality of life. The 40‐item Smell Identification Test (SIT) is widely used to assess psychophysical olfaction, but a CF‐specific minimal clinically important difference (MCID) has not been established. This study aimed to determine the SIT MCID in PwCF treated with elexacaftor/tezacaftor/ivacaftor (ETI) and/or endoscopic sinus surgery (ESS).


Methods
Data from three prospective, multi‐institutional observational studies were pooled. Participants were ≥12 years old with confirmed CF and CRS who completed SIT at baseline and ≥1 follow‐up (3, 6, 9, 12, or 24 months). Distribution‐based MCIDs were calculated using four methods: standard error of measurement (SEM), minimal detectable change (MDC = 1.96 × SEM), 0.5 × baseline standard deviation (SD), and 0.5 × SD of change scores (ΔSD).


Results
A total of 122 participants were enrolled (mean age 32.9 years, 54% female). Of these, 99 contributed follow‐up SIT scores (79 ETI, 20 ESS). SIT scores remained stable with ETI, with a small but statistically significant decline at 6 months (−1.4, p = 0.02). ESS was associated with mean gains of 3.1–4.5 points at early follow‐up, though these did not reach significance. Pooled distribution‐based MCID estimates ranged from 2 to 4 points, with an overall threshold of 3.1 (95% CI: 2.1–4.1).


Conclusions
This CF‐specific SIT threshold provides a clinically interpretable cut‐off for assessing olfaction. These findings establish a foundation for future work and highlight the importance of developing disease‐specific MCIDs to guide clinical care and research.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis (CRS) and olfactory dysfunction (OD) are highly prevalent among people with cystic fibrosis (PwCF) and negatively impact quality of life. The 40-item Smell Identification Test (SIT) is widely used to assess psychophysical olfaction, but a CF-specific minimal clinically important difference (MCID) has not been established. This study aimed to determine the SIT MCID in PwCF treated with elexacaftor/tezacaftor/ivacaftor (ETI) and/or endoscopic sinus surgery (ESS).&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Data from three prospective, multi-institutional observational studies were pooled. Participants were ≥12 years old with confirmed CF and CRS who completed SIT at baseline and ≥1 follow-up (3, 6, 9, 12, or 24 months). Distribution-based MCIDs were calculated using four methods: standard error of measurement (SEM), minimal detectable change (MDC = 1.96 × SEM), 0.5 × baseline standard deviation (SD), and 0.5 × SD of change scores (ΔSD).&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;A total of 122 participants were enrolled (mean age 32.9 years, 54% female). Of these, 99 contributed follow-up SIT scores (79 ETI, 20 ESS). SIT scores remained stable with ETI, with a small but statistically significant decline at 6 months (−1.4, &lt;i&gt;p&lt;/i&gt; = 0.02). ESS was associated with mean gains of 3.1–4.5 points at early follow-up, though these did not reach significance. Pooled distribution-based MCID estimates ranged from 2 to 4 points, with an overall threshold of 3.1 (95% CI: 2.1–4.1).&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;This CF-specific SIT threshold provides a clinically interpretable cut-off for assessing olfaction. These findings establish a foundation for future work and highlight the importance of developing disease-specific MCIDs to guide clinical care and research.&lt;/p&gt;</content:encoded>
         <dc:creator>
Eugene Oh, 
Jessa E. Miller, 
Michelle J. Lee, 
Anna Zemke, 
David Baraghoshi, 
Matthew J. Strand, 
Jeremiah A. Alt, 
Todd E. Bodner, 
Michael Chang, 
Naweed I. Chowdhury, 
Patricia H. Eshaghian, 
Anne E. Getz, 
Jennifer L. Goralski, 
David A. Gudis, 
Peter H. Hwang, 
Ashoke Khanwalkar, 
Adam J. Kimple, 
Jivianne T. Lee, 
Douglas A. Li, 
Jess C. Mace, 
Jayakar V. Nayak, 
Jonathan B. Overdevest, 
Zara Patel, 
Daniella K. Safatian, 
Rodney J. Schlosser, 
Brent Senior, 
Amanda L. Stapleton, 
Timothy L. Smith, 
Zachary M. Soler, 
Jeffrey D. Suh, 
Grant A. Turner, 
Marilene B. Wang, 
Milene T. Saavedra, 
Jennifer L. Taylor‐Cousar, 
Daniel M. Beswick
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Determining the Minimal Clinically Important Difference of the 40‐Item Smell Identification Test in People With Cystic Fibrosis</dc:title>
         <dc:identifier>10.1002/alr.70136</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70136</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70136?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70126?af=R</link>
         <pubDate>Thu, 05 Mar 2026 00:31:34 -0800</pubDate>
         <dc:date>2026-03-05T12:31:34-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70126</guid>
         <title>Endoscopic Posterior Nasal Neurectomy Versus Radiofrequency Ablation in Refractory Allergic Rhinitis: A 2‐Year Randomized Controlled Trial of Clinical Outcomes and Immunomodulatory Responses</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Endoscopic posterior nasal nerve (PNN) neurectomy and temperature‐controlled radiofrequency ablation are validated interventions for medication‐refractory allergic rhinitis (AR), but direct comparisons of their long‐term efficacy, safety, and mechanisms remain lacking.


Methods
In this prospective, multicenter, randomized, patient‐blinded study, 174 adults with moderate‐to‐severe persistent AR were allocated to PNN neurectomy (n = 89) or ablation (n = 85). The primary endpoint was the percentage of participants achieving the minimal clinically important difference (MCID) for the 24‐h reflective total nasal symptom score (rTNSS) at 24 months.


Results
The rTNSS MCID responder rate at 24 months was 86.5% (95% confidence interval [CI], 80.0–95.0%) in the neurectomy group and 84.9% (95% CI, 78.0–94.0%) in the ablation group, with no significant between‐group difference (p = 0.453). Both groups demonstrated substantial and parallel improvements in quality of life. Neurectomy provided greater and more durable control of rhinorrhea (1–24 months, all p &lt; 0.05), nasal congestion (24 months, p &lt; 0.001), and nasal itching (24 months, p = 0.046), alongside a greater reduction in unilateral nasal resistance (right side, p = 0.014). Both groups showed convergent systemic neuroimmune reprogramming at 1 year, with suppression of substance P, interleukin (IL)‐31, IL‐33, IL‐4, IL‐13, and IL‐6, and increased transforming growth factor‐β (TGF‐β)and immunoglobulin G4 (IgG4). No serious adverse events occurred; mild transitory events were reported only with neurectomy (3.4%).


Conclusion
Both techniques are effective and safe for refractory AR over 2 years. Although overall outcomes are comparable, neurectomy offers superior and sustained control of rhinorrhea, nasal congestion, and nasal itching. Treatment can be individualized based on symptom profile.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Endoscopic posterior nasal nerve (PNN) neurectomy and temperature-controlled radiofrequency ablation are validated interventions for medication-refractory allergic rhinitis (AR), but direct comparisons of their long-term efficacy, safety, and mechanisms remain lacking.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;In this prospective, multicenter, randomized, patient-blinded study, 174 adults with moderate-to-severe persistent AR were allocated to PNN neurectomy (&lt;i&gt;n&lt;/i&gt; = 89) or ablation (&lt;i&gt;n&lt;/i&gt; = 85). The primary endpoint was the percentage of participants achieving the minimal clinically important difference (MCID) for the 24-h reflective total nasal symptom score (rTNSS) at 24 months.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;The rTNSS MCID responder rate at 24 months was 86.5% (95% confidence interval [CI], 80.0–95.0%) in the neurectomy group and 84.9% (95% CI, 78.0–94.0%) in the ablation group, with no significant between-group difference (&lt;i&gt;p&lt;/i&gt; = 0.453). Both groups demonstrated substantial and parallel improvements in quality of life. Neurectomy provided greater and more durable control of rhinorrhea (1–24 months, all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05), nasal congestion (24 months, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.001), and nasal itching (24 months, &lt;i&gt;p&lt;/i&gt; = 0.046), alongside a greater reduction in unilateral nasal resistance (right side, &lt;i&gt;p&lt;/i&gt; = 0.014). Both groups showed convergent systemic neuroimmune reprogramming at 1 year, with suppression of substance P, interleukin (IL)-31, IL-33, IL-4, IL-13, and IL-6, and increased transforming growth factor-β (TGF-β)and immunoglobulin G4 (IgG4). No serious adverse events occurred; mild transitory events were reported only with neurectomy (3.4%).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Both techniques are effective and safe for refractory AR over 2 years. Although overall outcomes are comparable, neurectomy offers superior and sustained control of rhinorrhea, nasal congestion, and nasal itching. Treatment can be individualized based on symptom profile.&lt;/p&gt;</content:encoded>
         <dc:creator>
Rui Zheng, 
Xuekun Huang, 
Shuo Wu, 
Zhaohui Shi, 
Kai Wang, 
Huijun Qiu, 
Tian Yuan, 
Chuanliang Zhao, 
Jianhui Zhao, 
Weihao Wang, 
Zhenhao Xiao, 
Jianfeng Liu, 
Shaoqing Yu, 
Qintai Yang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Endoscopic Posterior Nasal Neurectomy Versus Radiofrequency Ablation in Refractory Allergic Rhinitis: A 2‐Year Randomized Controlled Trial of Clinical Outcomes and Immunomodulatory Responses</dc:title>
         <dc:identifier>10.1002/alr.70126</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70126</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70126?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70133?af=R</link>
         <pubDate>Thu, 05 Mar 2026 00:00:00 -0800</pubDate>
         <dc:date>2026-03-05T12:00:00-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70133</guid>
         <title>Effect of Laser Posterior Nasal Neurolysis for the Treatment of Chronic Rhinitis: A Randomized Controlled Trial</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
To determine the safety and efficacy of laser ablation of the posterior nasal nerve (PNN) for the treatment of chronic rhinitis.


Methods
This study was a single‐center, prospective, single‐blinded, randomized sham‐controlled trial. Patients with a 24‐h reflective Total Nasal Symptom Score (rTNSS) ≧ 5, rhinorrhea ≧ 2, and congestion ≧ 1, were randomized 2:1 to active PNN treatment with a CO2 laser device or a sham procedure. Outcome measures included the rTNSS, Nasal Obstruction Symptom Evaluation (NOSE), Pittsburgh Sleep Quality Index (PSQI), and Epworth Sleepiness Scale (ESS). The primary endpoint was the change in scores at 3 months.


Results
Patients had a mean baseline rTNSS of 8.5 (95% CI, 7.9–9.1) and 8.2 (95% CI, 7.4–8.9) (p = 0.589) in the active treatment (n = 43) and sham control (n = 22) arms, respectively. At 3 months, the active treatment arm had a significantly greater decrease in rTNSS −4.7 (95% CI, −5.5 to −3.9) versus −2.6 (95% CI, −3.4 to −1.8) (p = 0.002). While the responder rate (RR, defined as ≧30% improvement rTNSS) was not significantly higher in the active treatment arm (81.4% vs. 63.6%, p = 0.119), post‐hoc analysis of RR (≧ 50% improvement) showed a significantly higher rate of 65.1% versus 31.8% (p = 0.011). There were greater improvements in the PSQI and ESS scores for the active arm over the sham arm at follow‐ups. (p = 0.041 and 0.005, respectively).


Conclusions
The CO2 laser posterior nasal neurolysis of the PNN area is associated with minimal adverse events and is superior to a sham procedure in reducing the symptom burden of chronic rhinitis.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;To determine the safety and efficacy of laser ablation of the posterior nasal nerve (PNN) for the treatment of chronic rhinitis.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This study was a single-center, prospective, single-blinded, randomized sham-controlled trial. Patients with a 24-h reflective Total Nasal Symptom Score (rTNSS) ≧ 5, rhinorrhea ≧ 2, and congestion ≧ 1, were randomized 2:1 to active PNN treatment with a CO&lt;sub&gt;2&lt;/sub&gt; laser device or a sham procedure. Outcome measures included the rTNSS, Nasal Obstruction Symptom Evaluation (NOSE), Pittsburgh Sleep Quality Index (PSQI), and Epworth Sleepiness Scale (ESS). The primary endpoint was the change in scores at 3 months.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Patients had a mean baseline rTNSS of 8.5 (95% CI, 7.9–9.1) and 8.2 (95% CI, 7.4–8.9) (&lt;i&gt;p&lt;/i&gt; = 0.589) in the active treatment (&lt;i&gt;n&lt;/i&gt; = 43) and sham control (n = 22) arms, respectively. At 3 months, the active treatment arm had a significantly greater decrease in rTNSS −4.7 (95% CI, −5.5 to −3.9) versus −2.6 (95% CI, −3.4 to −1.8) (&lt;i&gt;p&lt;/i&gt; = 0.002). While the responder rate (RR, defined as ≧30% improvement rTNSS) was not significantly higher in the active treatment arm (81.4% vs. 63.6%, &lt;i&gt;p&lt;/i&gt; = 0.119), post-hoc analysis of RR (≧ 50% improvement) showed a significantly higher rate of 65.1% versus 31.8% (&lt;i&gt;p&lt;/i&gt; = 0.011). There were greater improvements in the PSQI and ESS scores for the active arm over the sham arm at follow-ups. (&lt;i&gt;p = &lt;/i&gt;0.041 and 0.005, respectively).&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;The CO&lt;sub&gt;2&lt;/sub&gt; laser posterior nasal neurolysis of the PNN area is associated with minimal adverse events and is superior to a sham procedure in reducing the symptom burden of chronic rhinitis.&lt;/p&gt;</content:encoded>
         <dc:creator>
Jyun‐Yi Liao, 
En‐Ying Wang, 
Ying‐Shuo Hsu, 
Ming‐Shao Tsai, 
Cheng‐Jung Wu, 
Chia‐Hao Chang, 
Yi‐Li Hwang, 
Han‐Lo Teng, 
Jun‐Wei Hsieh, 
Chien‐Yu Huang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Effect of Laser Posterior Nasal Neurolysis for the Treatment of Chronic Rhinitis: A Randomized Controlled Trial</dc:title>
         <dc:identifier>10.1002/alr.70133</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70133</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70133?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70131?af=R</link>
         <pubDate>Mon, 02 Mar 2026 05:19:38 -0800</pubDate>
         <dc:date>2026-03-02T05:19:38-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70131</guid>
         <title>Using Local sIgE Threshold to Refine the Diagnosis of Local Allergic Rhinitis</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Local allergic rhinitis (LAR) is a chronic rhinitis (CR) phenotype with localized IgE production but no systemic atopy. Diagnosis relies on the nasal allergen challenge (NAC), but its correlation with the underlying immunological endotype is unclear, necessitating a more reliable biomarker. Therefore, this study was conducted to evaluate a local specific immunoglobulin E (sIgE) threshold for diagnosing house dust mite (HDM)‐sensitized LAR and compare its immunological relevance to the conventional NAC‐based method.


Methods
This prospective study enrolled 181 CR patients without systemic atopy and 146 healthy controls. All CR patients underwent NAC. Local sIgE levels of Dermatophagoides pteronyssinus and Dermatophagoides farinae were measured in nasal secretions. A diagnostic threshold was established using the 95th percentile from the healthy cohort. The NAC and sIgE‐based stratifications were then compared by analyzing patients’ nasal cytokine profiles.


Results
Classification based on NAC positivity did not reveal significant differences in local sIgE or a consistent type 2 inflammatory signature. In contrast, stratification using the established local sIgE threshold (≥ 0.14 kUA/L) identified a local sIgE‐high group with significantly elevated levels of type 2 cytokines (IL‐4, IL‐5, CCL5, and CCL11) compared to the sIgE‐low group (all p &lt; 0.05). Furthermore, local sIgE levels positively correlated with these type 2 cytokines in the sIgE‐high group.


Conclusion
A local sIgE threshold reliably identifies an immunologically distinct LAR endotype, aligning diagnosis with its type 2 pathophysiology. This biomarker‐driven approach offers a precise tool to refine diagnostic algorithms and improve patient selection for targeted therapies.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Local allergic rhinitis (LAR) is a chronic rhinitis (CR) phenotype with localized IgE production but no systemic atopy. Diagnosis relies on the nasal allergen challenge (NAC), but its correlation with the underlying immunological endotype is unclear, necessitating a more reliable biomarker. Therefore, this study was conducted to evaluate a local specific immunoglobulin E (sIgE) threshold for diagnosing house dust mite (HDM)-sensitized LAR and compare its immunological relevance to the conventional NAC-based method.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This prospective study enrolled 181 CR patients without systemic atopy and 146 healthy controls. All CR patients underwent NAC. Local sIgE levels of &lt;i&gt;Dermatophagoides pteronyssinus&lt;/i&gt; and &lt;i&gt;Dermatophagoides farinae&lt;/i&gt; were measured in nasal secretions. A diagnostic threshold was established using the 95th percentile from the healthy cohort. The NAC and sIgE-based stratifications were then compared by analyzing patients’ nasal cytokine profiles.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Classification based on NAC positivity did not reveal significant differences in local sIgE or a consistent type 2 inflammatory signature. In contrast, stratification using the established local sIgE threshold (≥ 0.14 kUA/L) identified a local sIgE-high group with significantly elevated levels of type 2 cytokines (IL-4, IL-5, CCL5, and CCL11) compared to the sIgE-low group (all &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05). Furthermore, local sIgE levels positively correlated with these type 2 cytokines in the sIgE-high group.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;A local sIgE threshold reliably identifies an immunologically distinct LAR endotype, aligning diagnosis with its type 2 pathophysiology. This biomarker-driven approach offers a precise tool to refine diagnostic algorithms and improve patient selection for targeted therapies.&lt;/p&gt;</content:encoded>
         <dc:creator>
Zengxiao Zhang, 
Xu Zhang, 
Jingyun Li, 
Yu Song, 
Lin Xi, 
Yu Zhang, 
Luo Zhang, 
Yuan Zhang
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Using Local sIgE Threshold to Refine the Diagnosis of Local Allergic Rhinitis</dc:title>
         <dc:identifier>10.1002/alr.70131</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70131</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70131?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70130?af=R</link>
         <pubDate>Mon, 02 Mar 2026 00:00:00 -0800</pubDate>
         <dc:date>2026-03-02T12:00:00-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70130</guid>
         <title>Olfactory Bulb Volume Reflects Olfactory Dysfunction and Network Organization: Insights From the Population‐Based Rhineland Study</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Olfactory dysfunction is common in aging and an early symptom of neurodegenerative diseases, but how structural (olfactory bulb [OB] volume) and functional (olfactory network [OFN] functional connectivity [FC]) brain features interact to shape odor identification ability remains unclear. Therefore, we assessed the interrelations among OB volume, OFN FC, and odor identification ability in a large population‐based cohort.


Methods
Using cross‐sectional data from 5605 participants of the Rhineland Study (age range: 30–95 years), we extracted OB volume and OFN FC from 3T MRI scans. Odor identification was examined with the 12‐item “Sniffin’ Sticks” test. Using linear regression, we examined the relations between OB volume, OFN FC, and odor identification.


Results
A smaller OB was associated with worse odor identification (standardized β = 0.09, 95% confidence interval: 0.06–0.12). This association was stronger in men and strongest in older individuals of both sexes. Only in participants with a large OB, lower OFN FC was significantly associated with worse odor identification (standardized β between 0.03 and 0.12), especially among older participants (62–95 years) and in memory‐related regions (hippocampus, amygdala, and orbitofrontal cortex).


Conclusion
Our findings demonstrate the importance of OB volume in detecting olfactory dysfunction. Moreover, they reveal that the OB contributes to odor identification both directly and by modulating central network function, offering new insights into olfactory dysfunction as a potential biomarker for neurodegeneration.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Olfactory dysfunction is common in aging and an early symptom of neurodegenerative diseases, but how structural (olfactory bulb [OB] volume) and functional (olfactory network [OFN] functional connectivity [FC]) brain features interact to shape odor identification ability remains unclear. Therefore, we assessed the interrelations among OB volume, OFN FC, and odor identification ability in a large population-based cohort.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;Using cross-sectional data from 5605 participants of the Rhineland Study (age range: 30–95 years), we extracted OB volume and OFN FC from 3T MRI scans. Odor identification was examined with the 12-item “Sniffin’ Sticks” test. Using linear regression, we examined the relations between OB volume, OFN FC, and odor identification.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;A smaller OB was associated with worse odor identification (standardized &lt;i&gt;β&lt;/i&gt; = 0.09, 95% confidence interval: 0.06–0.12). This association was stronger in men and strongest in older individuals of both sexes. Only in participants with a large OB, lower OFN FC was significantly associated with worse odor identification (standardized &lt;i&gt;β&lt;/i&gt; between 0.03 and 0.12), especially among older participants (62–95 years) and in memory-related regions (hippocampus, amygdala, and orbitofrontal cortex).&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Our findings demonstrate the importance of OB volume in detecting olfactory dysfunction. Moreover, they reveal that the OB contributes to odor identification both directly and by modulating central network function, offering new insights into olfactory dysfunction as a potential biomarker for neurodegeneration.&lt;/p&gt;</content:encoded>
         <dc:creator>
Weiyi Zeng, 
Konstantinos Melas, 
Santiago Estrada, 
N. Ahmad Aziz, 
Monique M. B. Breteler
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Olfactory Bulb Volume Reflects Olfactory Dysfunction and Network Organization: Insights From the Population‐Based Rhineland Study</dc:title>
         <dc:identifier>10.1002/alr.70130</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70130</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70130?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70125?af=R</link>
         <pubDate>Mon, 02 Mar 2026 00:00:00 -0800</pubDate>
         <dc:date>2026-03-02T12:00:00-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70125</guid>
         <title>Dosing Interval Extension of Dupilumab in CRSwNP: Five‐Year Real World Outcomes</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis with nasal polyps (CRSwNP) is a persistent, often Type 2‐mediated inflammatory disease that markedly impairs quality of life. While dupilumab provides rapid improvement, there is limited evidence on long‐term outcomes beyond 2 years, and the clinical impact of dosing‐interval extension remains unclear. We therefore set out to evaluate long‐term real‐world outcomes of dupilumab therapy in CRSwNP and assess the effectiveness and safety of dosing‐interval extension after achieving disease control.


Methods
This retrospective single‐center cohort included 224 adults with CRSwNP (37% with nonsteroidal anti‐inflammatory drug‐exacerbated respiratory disease) treated with dupilumab for up to 4.5 years with outcomes modeled to 5 years. Longitudinal changes in polyp size, symptom burden, olfaction, asthma control, and Type 2 biomarkers were analyzed using mixed‐effects models. Outcomes were then compared between patients who maintained standard 2‐week dosing and those who voluntarily extended dosing intervals after achieving stable control.


Results
Dupilumab led to significant improvements in polyp burden, olfactory function, and quality of life peaking within 6 months, with sustained benefit through 5 years according to longitudinal modeling. Forty percent of patients extended dosing intervals without loss of efficacy and reported fewer treatment‐related adverse events. Overall, 16% experienced side effects, most commonly musculoskeletal complaints, followed by skin reactions and injection site reactions.


Conclusion
Long‐term dupilumab therapy provided durable disease control and excellent safety. Personalized dosing‐interval extension maintained efficacy and reduced treatment burden, supporting its potential role in optimizing long‐term management of CRSwNP, especially in patients with troublesome side effects.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis with nasal polyps (CRSwNP) is a persistent, often Type 2-mediated inflammatory disease that markedly impairs quality of life. While dupilumab provides rapid improvement, there is limited evidence on long-term outcomes beyond 2 years, and the clinical impact of dosing-interval extension remains unclear. We therefore set out to evaluate long-term real-world outcomes of dupilumab therapy in CRSwNP and assess the effectiveness and safety of dosing-interval extension after achieving disease control.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This retrospective single-center cohort included 224 adults with CRSwNP (37% with nonsteroidal anti-inflammatory drug-exacerbated respiratory disease) treated with dupilumab for up to 4.5 years with outcomes modeled to 5 years. Longitudinal changes in polyp size, symptom burden, olfaction, asthma control, and Type 2 biomarkers were analyzed using mixed-effects models. Outcomes were then compared between patients who maintained standard 2-week dosing and those who voluntarily extended dosing intervals after achieving stable control.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Dupilumab led to significant improvements in polyp burden, olfactory function, and quality of life peaking within 6 months, with sustained benefit through 5 years according to longitudinal modeling. Forty percent of patients extended dosing intervals without loss of efficacy and reported fewer treatment-related adverse events. Overall, 16% experienced side effects, most commonly musculoskeletal complaints, followed by skin reactions and injection site reactions.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Long-term dupilumab therapy provided durable disease control and excellent safety. Personalized dosing-interval extension maintained efficacy and reduced treatment burden, supporting its potential role in optimizing long-term management of CRSwNP, especially in patients with troublesome side effects.&lt;/p&gt;</content:encoded>
         <dc:creator>
Nicholas J. Campion, 
Dioni‐Pinelopi Petsiou, 
Florian C. Fally, 
Karina Berbalk, 
Noah F. Melamed, 
Aldine Tu, 
Christina Morgenstern, 
Fana Alem Kidane, 
Mohammed Zghaebi, 
Linda Liu, 
Minghao Pan, 
Tina J. Bartosik, 
Victoria Stanek, 
Katarina Gangl, 
Julia Eckl‐Dorna, 
Sven Schneider
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Dosing Interval Extension of Dupilumab in CRSwNP: Five‐Year Real World Outcomes</dc:title>
         <dc:identifier>10.1002/alr.70125</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70125</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70125?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70128?af=R</link>
         <pubDate>Fri, 27 Feb 2026 07:14:41 -0800</pubDate>
         <dc:date>2026-02-27T07:14:41-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70128</guid>
         <title>Uncovering Cystic Fibrosis Carrier: Insights From a Heterozygous CFTR‐F508del Rabbit Model</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis (CRS) is a heterogeneous inflammatory disorder frequently associated with impaired mucociliary clearance and bacterial infection. Individuals carrying a single cystic fibrosis transmembrane conductance regulator (CFTR) mutation exhibit partial CFTR dysfunction and are increasingly recognized as being at risk for CRS; however, the sinonasal phenotype and host–pathogen interactions in CF carriers remain poorly defined.


Methods
We characterized heterozygous ΔF508 CF rabbits (heterozygous, n = 6) compared with wild‐type (WT) (n = 5). Baseline sinonasal structure was assessed by computed tomography and histology. CFTR function was measured by nasal potential difference (NPD) and Ussing chamber analysis of primary epithelial cultures, with or without CFTR modulators. Bacterial sinusitis was induced using Pseudomonas aeruginosa (PA14), followed by longitudinal imaging, bacterial quantification, histology, and PA14 RNA sequencing.


Results
Heterozygous rabbits demonstrated significant sinus hypoplasia compared with WT (mm3: heterozygous 77.9 vs. WT 108.1 mm3, p &lt; 0.01) without spontaneous sinusitis. NPD revealed ∼50% reduction in chloride transport relative to WT (∆mV: heterozygous −15.5 vs. WT −35.8, p &lt; 0.01). CFTR modulation partially restored chloride secretion in epithelial cells from heterozygous to ∼80% of WT (p &lt; 0.0001). Following P. aeruginosa inoculation, heterozygous rabbits exhibited higher bacterial burden (p &lt; 0.05), persistent radiographic opacification (week 4, p &lt; 0.01), and delayed histologic recovery. PA14 RNAseq revealed a distinct transcriptional profile in the heterozygous sinonasal environment.


Conclusions
Heterozygous ΔF508 CF rabbits recapitulate key sinonasal features relevant to CF carriers, including reduced CFTR function, altered host defense, and impaired infection clearance. This model provides a translational platform for investigating CRS pathogenesis and evaluating CFTR‐targeted therapies in CF carriers.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis (CRS) is a heterogeneous inflammatory disorder frequently associated with impaired mucociliary clearance and bacterial infection. Individuals carrying a single cystic fibrosis transmembrane conductance regulator (CFTR) mutation exhibit partial CFTR dysfunction and are increasingly recognized as being at risk for CRS; however, the sinonasal phenotype and host–pathogen interactions in CF carriers remain poorly defined.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We characterized heterozygous &lt;i&gt;ΔF508&lt;/i&gt; CF rabbits (heterozygous, &lt;i&gt;n&lt;/i&gt; = 6) compared with wild-type (WT) (&lt;i&gt;n&lt;/i&gt; = 5). Baseline sinonasal structure was assessed by computed tomography and histology. CFTR function was measured by nasal potential difference (NPD) and Ussing chamber analysis of primary epithelial cultures, with or without CFTR modulators. Bacterial sinusitis was induced using &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; (PA14), followed by longitudinal imaging, bacterial quantification, histology, and PA14 RNA sequencing.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Heterozygous rabbits demonstrated significant sinus hypoplasia compared with WT (mm&lt;sup&gt;3&lt;/sup&gt;: heterozygous 77.9 vs. WT 108.1 mm&lt;sup&gt;3&lt;/sup&gt;, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.01) without spontaneous sinusitis. NPD revealed ∼50% reduction in chloride transport relative to WT (∆mV: heterozygous −15.5 vs. WT −35.8, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.01). CFTR modulation partially restored chloride secretion in epithelial cells from heterozygous to ∼80% of WT (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.0001). Following &lt;i&gt;P. aeruginosa&lt;/i&gt; inoculation, heterozygous rabbits exhibited higher bacterial burden (&lt;i&gt;p&lt;/i&gt; &amp;lt; 0.05), persistent radiographic opacification (week 4, &lt;i&gt;p&lt;/i&gt; &amp;lt; 0.01), and delayed histologic recovery. PA14 RNAseq revealed a distinct transcriptional profile in the heterozygous sinonasal environment.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Heterozygous &lt;i&gt;ΔF508&lt;/i&gt; CF rabbits recapitulate key sinonasal features relevant to CF carriers, including reduced CFTR function, altered host defense, and impaired infection clearance. This model provides a translational platform for investigating CRS pathogenesis and evaluating CFTR-targeted therapies in CF carriers.&lt;/p&gt;</content:encoded>
         <dc:creator>
Do‐Yeon Cho, 
Alexis E. McFeely, 
Daniel Skinner, 
Shaoyan Zhang, 
Justin Hedvat, 
Weslee Ping‐ay, 
Daniel M. Beswick, 
Justin H. Turner, 
Bradford A. Woodworth, 
Jie Xu
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Uncovering Cystic Fibrosis Carrier: Insights From a Heterozygous CFTR‐F508del Rabbit Model</dc:title>
         <dc:identifier>10.1002/alr.70128</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70128</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70128?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70121?af=R</link>
         <pubDate>Fri, 20 Feb 2026 03:42:26 -0800</pubDate>
         <dc:date>2026-02-20T03:42:26-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70121</guid>
         <title>Cost Utility Analysis of Fluticasone Exhalation Delivery System Versus Budesonide Nasal Irrigation for Chronic Rhinosinusitis With Nasal Polyps</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Chronic rhinosinusitis with nasal polyps (CRSwNP) is managed after sinus surgery with topical corticosteroids. Given limited distribution of nasal steroid sprays, patients have the option of either steroid nasal irrigation (SNI) or exhalation delivery system with fluticasone (EDS‐FLU). This study evaluates the cost‐effectiveness of EDS‐FLU compared to SNI for CRSwNP.


Methods
A cohort‐style Markov decision‐tree economic model with a 33‐year time horizon was developed in TreeAgePro. Because EDS‐FLU is not currently covered by Medicare, costs of medications were estimated using retail pricing. A willingness‐to‐pay threshold of $50,000/quality adjusted life year (QALY) was used to determine cost‐effectiveness. One‐way and probabilistic sensitivity analysis was conducted using 10,000 Monte Carlo simulations.


Results
EDS‐FLU had an incremental benefit of 0.41 QALYs compared to SNI. In base case analysis, EDS‐FLU costs $140,966.63 after the study period, whereas SNI costs $40,817.50. With an ICER of $244,185.37/QALY, SNI is the more cost‐effective strategy. Probabilistic sensitivity analysis reported SNI as the cost‐effective strategy in 98.50% of simulations.


Conclusions
Compared to EDS‐FLU, SNI is the cost‐effective strategy for treating CRSwNP following FESS. Changes in drug pricing and improvements in patient selection may cause adjustments in the most cost‐effective strategy for CRSwNP management.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis with nasal polyps (CRSwNP) is managed after sinus surgery with topical corticosteroids. Given limited distribution of nasal steroid sprays, patients have the option of either steroid nasal irrigation (SNI) or exhalation delivery system with fluticasone (EDS-FLU). This study evaluates the cost-effectiveness of EDS-FLU compared to SNI for CRSwNP.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A cohort-style Markov decision-tree economic model with a 33-year time horizon was developed in TreeAgePro. Because EDS-FLU is not currently covered by Medicare, costs of medications were estimated using retail pricing. A willingness-to-pay threshold of $50,000/quality adjusted life year (QALY) was used to determine cost-effectiveness. One-way and probabilistic sensitivity analysis was conducted using 10,000 Monte Carlo simulations.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;EDS-FLU had an incremental benefit of 0.41 QALYs compared to SNI. In base case analysis, EDS-FLU costs $140,966.63 after the study period, whereas SNI costs $40,817.50. With an ICER of $244,185.37/QALY, SNI is the more cost-effective strategy. Probabilistic sensitivity analysis reported SNI as the cost-effective strategy in 98.50% of simulations.&lt;/p&gt;
&lt;h2&gt;Conclusions&lt;/h2&gt;
&lt;p&gt;Compared to EDS-FLU, SNI is the cost-effective strategy for treating CRSwNP following FESS. Changes in drug pricing and improvements in patient selection may cause adjustments in the most cost-effective strategy for CRSwNP management.&lt;/p&gt;</content:encoded>
         <dc:creator>
Daniel Xiao, 
Martin J. Citardi, 
William C. Yao, 
Amber U. Luong
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Cost Utility Analysis of Fluticasone Exhalation Delivery System Versus Budesonide Nasal Irrigation for Chronic Rhinosinusitis With Nasal Polyps</dc:title>
         <dc:identifier>10.1002/alr.70121</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70121</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70121?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70123?af=R</link>
         <pubDate>Fri, 20 Feb 2026 03:40:12 -0800</pubDate>
         <dc:date>2026-02-20T03:40:12-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70123</guid>
         <title>Altered Nasal Microbiota in Sinonasal Tumors: A Comparative Analysis of Malignant and Benign Sinonasal Tumors</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Although shifts in nasal microbiota have been well‐documented in inflammatory upper airway conditions, microbiota tumor‐associated alterations remain uncharacterized. This study is the first to compare sinonasal microbiota profiles of patients with malignant tumors (MT), benign tumors (BT), and controls, offering insights into tumor‐associated microbiomes.


Methods
This prospective, cross‐sectional, observational study assessed intraoperative sinus swabs from 70 adult research participants (MT = 23, BT = 15, control = 32). Sinonasal microbial communities were characterized using 16S rRNA gene amplicon sequencing to determine if microbial community structures differed between groups.


Results
Tumor‐associated sinonasal microbiota profiles showed clear dysbiosis, with reduced relative abundance of beneficial microbes and increased putative pathogenic taxa. Both MT and BT had significantly lower microbial diversity and distinct compositions compared to controls. MT samples had significantly higher relative abundance of Firmicutes and reduced relative abundance of Actinobacteria. These phylum‐level alterations were accompanied by elevated proinflammatory microbial taxa, paired with reduced relative abundance of keystone, beneficial taxa consistent with healthy nasal microbiomes. Microbial communities in BT and MT samples were similar, but Alcaligenes was more abundant, and Corynebacterium was less abundant in MT than in BT.


Conclusion
This study observed that sinonasal microbial communities in MT exhibited marked dysbiosis with a reduction in the relative abundance of putative sinonasal commensal taxa compared to controls. These alterations were present to a lesser extent in BT. Future investigations should aim to determine whether these microbial shifts contribute to tumor development or represent secondary effects, with an aim to quantify their impact on outcomes and guide therapeutic strategies.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Although shifts in nasal microbiota have been well-documented in inflammatory upper airway conditions, microbiota tumor-associated alterations remain uncharacterized. This study is the first to compare sinonasal microbiota profiles of patients with malignant tumors (MT), benign tumors (BT), and controls, offering insights into tumor-associated microbiomes.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;This prospective, cross-sectional, observational study assessed intraoperative sinus swabs from 70 adult research participants (MT = 23, BT = 15, control = 32). Sinonasal microbial communities were characterized using 16S rRNA gene amplicon sequencing to determine if microbial community structures differed between groups.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Tumor-associated sinonasal microbiota profiles showed clear dysbiosis, with reduced relative abundance of beneficial microbes and increased putative pathogenic taxa. Both MT and BT had significantly lower microbial diversity and distinct compositions compared to controls. MT samples had significantly higher relative abundance of Firmicutes and reduced relative abundance of Actinobacteria. These phylum-level alterations were accompanied by elevated proinflammatory microbial taxa, paired with reduced relative abundance of keystone, beneficial taxa consistent with healthy nasal microbiomes. Microbial communities in BT and MT samples were similar, but &lt;i&gt;Alcaligenes&lt;/i&gt; was more abundant, and &lt;i&gt;Corynebacterium&lt;/i&gt; was less abundant in MT than in BT.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;This study observed that sinonasal microbial communities in MT exhibited marked dysbiosis with a reduction in the relative abundance of putative sinonasal commensal taxa compared to controls. These alterations were present to a lesser extent in BT. Future investigations should aim to determine whether these microbial shifts contribute to tumor development or represent secondary effects, with an aim to quantify their impact on outcomes and guide therapeutic strategies.&lt;/p&gt;</content:encoded>
         <dc:creator>
Evan A. Patel, 
Phillip A. Engen, 
Glen D. Souza, 
Sarah Khalife, 
Donyea Moore, 
Lauren Kret, 
Pedro Escobedo, 
Stefan J. Green, 
Ankur Naqib, 
Peter Filip, 
Peter Papagiannopoulos, 
Bobby A. Tajudeen, 
Mahboobeh Mahdavinia, 
Pete S. Batra
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Altered Nasal Microbiota in Sinonasal Tumors: A Comparative Analysis of Malignant and Benign Sinonasal Tumors</dc:title>
         <dc:identifier>10.1002/alr.70123</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70123</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70123?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70112?af=R</link>
         <pubDate>Fri, 13 Feb 2026 09:20:11 -0800</pubDate>
         <dc:date>2026-02-13T09:20:11-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70112</guid>
         <title>Effect of Budesonide Nasal Irrigation in Patients With Chronic Rhinosinusitis With Nasal Polyps Without Prior Sinus Surgery: A Randomized, Double‐Blind, Placebo‐Controlled Study</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
The indication for nasal irrigation with corticosteroids after sinus surgery in patients with Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) is well established, as surgery facilitates distribution throughout the sinonasal cavity. However, it remains unknown whether this approach could also provide therapeutic benefit prior to surgery. This study aims to compare the effect of budesonide versus saline nasal irrigation in surgically naive CRSwNP patients.


Methods
A randomized, double‐blind, placebo‐controlled parallel‐group study was conducted in 52 patients with diffuse type 2 CRSwNP with no previous sinus surgery. Patients were randomized to receive either 1 mg budesonide or saline nasal irrigation twice daily for four weeks. The primary outcome was the change in the 22‐item Sinonasal Outcome Test (SNOT‐22). Secondary outcomes included the Visual Analogue Scale (VAS), Nasal Polyp Score (NPS), and the Connecticut (CCCRC) olfactory test.


Results
A total of 52 patients were randomized (mean age 50.1 ± 12.9 years; 51.9% female). The intention‐to‐treat (ITT) analysis showed that the budesonide nasal irrigation group demonstrated a significantly greater improvement in SNOT‐22 (mean difference: 18.1 points [95% CI: 3.4 to 32.8; p = 0.017]), VAS (mean difference 2.24 points [95% CI: 0.35 to 4.13; p = 0.018]) and NPS (mean difference: 0.73 points [95% CI: 0.25 to 1.21]; p = 0.003). No significant differences were observed between groups in CCCRC.


Conclusion
Budesonide nasal irrigation may be an important tool for controlling sinonasal symptoms in patients with CRSwNP who are not candidates for sinus surgery or while awaiting surgical treatment.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;The indication for nasal irrigation with corticosteroids after sinus surgery in patients with Chronic Rhinosinusitis with Nasal Polyps (CRSwNP) is well established, as surgery facilitates distribution throughout the sinonasal cavity. However, it remains unknown whether this approach could also provide therapeutic benefit prior to surgery. This study aims to compare the effect of budesonide versus saline nasal irrigation in surgically naive CRSwNP patients.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A randomized, double-blind, placebo-controlled parallel-group study was conducted in 52 patients with diffuse type 2 CRSwNP with no previous sinus surgery. Patients were randomized to receive either 1 mg budesonide or saline nasal irrigation twice daily for four weeks. The primary outcome was the change in the 22-item Sinonasal Outcome Test (SNOT-22). Secondary outcomes included the Visual Analogue Scale (VAS), Nasal Polyp Score (NPS), and the Connecticut (CCCRC) olfactory test.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;A total of 52 patients were randomized (mean age 50.1 ± 12.9 years; 51.9% female). The intention-to-treat (ITT) analysis showed that the budesonide nasal irrigation group demonstrated a significantly greater improvement in SNOT-22 (mean difference: 18.1 points [95% CI: 3.4 to 32.8; &lt;i&gt;p =&lt;/i&gt; 0.017]), VAS (mean difference 2.24 points [95% CI: 0.35 to 4.13; &lt;i&gt;p =&lt;/i&gt; 0.018]) and NPS (mean difference: 0.73 points [95% CI: 0.25 to 1.21]; &lt;i&gt;p =&lt;/i&gt; 0.003). No significant differences were observed between groups in CCCRC.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Budesonide nasal irrigation may be an important tool for controlling sinonasal symptoms in patients with CRSwNP who are not candidates for sinus surgery or while awaiting surgical treatment.&lt;/p&gt;</content:encoded>
         <dc:creator>
Juliana Sant'Ana, 
Isabela Pontes, 
Caio Floriano, 
Renato Rios, 
Marlos Cortez, 
Marcel Miyake
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Effect of Budesonide Nasal Irrigation in Patients With Chronic Rhinosinusitis With Nasal Polyps Without Prior Sinus Surgery: A Randomized, Double‐Blind, Placebo‐Controlled Study</dc:title>
         <dc:identifier>10.1002/alr.70112</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70112</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70112?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70113?af=R</link>
         <pubDate>Fri, 06 Feb 2026 06:49:19 -0800</pubDate>
         <dc:date>2026-02-06T06:49:19-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70113</guid>
         <title>Moderate to Vigorous Physical Activity and Chronic Rhinosinusitis Risk: A Longitudinal Fitbit Study</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Introduction
Chronic rhinosinusitis (CRS) is an inflammatory condition of the sinonasal mucosa. While physical activity is known to modulate systemic inflammation, its role in CRS prevention remains unclear. This study evaluates the association between moderate to vigorous physical activity (MVPA) and CRS using longitudinal Fitbit data.


Methods
We conducted a retrospective cohort study within the All of Us Research Program using Fitbit‐derived activity data linked to electronic health records. Adults with ≥ 1 year of valid data were eligible. MVPA was averaged across “strict weeks” (7 valid days, &gt; 100 steps/day) and categorized as &lt; 75, 75–150, 150–225, 225–300, or &gt; 300 min. CRS was defined using ICD‐10 coding. Propensity score matching was performed on demographics, obesity, and smoking status. Kaplan–Meier curves, Cochran–Mantel–Haenszel odds ratios, and fixed‐effects models assessed associations between MVPA and CRS.


Results
The matched cohort included 583 CRSsNP cases and 583 controls. Kaplan–Meier survival analysis demonstrated significant separation across MVPA groups (p = 0.0099), with higher activity associated with lower cumulative incidence. Participants exercising 75–150 min/week had nearly twice the odds of CRS compared with those exercising 150–225 min (OR = 1.95, 95% CI 1.07–3.55). Timing models showed earlier diagnoses among the least active group (− 152 weeks, 95% CI − 169 to − 134) and later diagnoses among those exercising &gt; 300 min/week (+ 260 weeks, 95% CI + 200 to + 320). Continuous modeling revealed an inverse dose‐response with a plateau beyond 300 min.


Conclusion
Regular MVPA is associated with reduced CRS incidence and prolonged disease‐free years, supporting physical activity as a possible modifiable risk factor for CRS.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Introduction&lt;/h2&gt;
&lt;p&gt;Chronic rhinosinusitis (CRS) is an inflammatory condition of the sinonasal mucosa. While physical activity is known to modulate systemic inflammation, its role in CRS prevention remains unclear. This study evaluates the association between moderate to vigorous physical activity (MVPA) and CRS using longitudinal Fitbit data.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;We conducted a retrospective cohort study within the All of Us Research Program using Fitbit-derived activity data linked to electronic health records. Adults with ≥ 1 year of valid data were eligible. MVPA was averaged across “strict weeks” (7 valid days, &amp;gt; 100 steps/day) and categorized as &amp;lt; 75, 75–150, 150–225, 225–300, or &amp;gt; 300 min. CRS was defined using ICD-10 coding. Propensity score matching was performed on demographics, obesity, and smoking status. Kaplan–Meier curves, Cochran–Mantel–Haenszel odds ratios, and fixed-effects models assessed associations between MVPA and CRS.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;The matched cohort included 583 CRSsNP cases and 583 controls. Kaplan–Meier survival analysis demonstrated significant separation across MVPA groups (&lt;i&gt;p&lt;/i&gt; = 0.0099), with higher activity associated with lower cumulative incidence. Participants exercising 75–150 min/week had nearly twice the odds of CRS compared with those exercising 150–225 min (OR = 1.95, 95% CI 1.07–3.55). Timing models showed earlier diagnoses among the least active group (− 152 weeks, 95% CI − 169 to − 134) and later diagnoses among those exercising &amp;gt; 300 min/week (+ 260 weeks, 95% CI + 200 to + 320). Continuous modeling revealed an inverse dose-response with a plateau beyond 300 min.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;Regular MVPA is associated with reduced CRS incidence and prolonged disease-free years, supporting physical activity as a possible modifiable risk factor for CRS.&lt;/p&gt;</content:encoded>
         <dc:creator>
Heli Majeethia, 
Aakash Agarwal, 
Ahmed Abdou, 
Jagan Dwarampudi, 
Justina Varghese, 
Renjie Hu, 
Zain Mehdi, 
Tania Banerjee, 
Vivek Pandrangi, 
Arthur Wu, 
Dennis Tang, 
Masayoshi Takashima, 
Omar G. Ahmed
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Moderate to Vigorous Physical Activity and Chronic Rhinosinusitis Risk: A Longitudinal Fitbit Study</dc:title>
         <dc:identifier>10.1002/alr.70113</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70113</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70113?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
      </item>
      <item>
         <link>https://onlinelibrary.wiley.com/doi/10.1002/alr.70114?af=R</link>
         <pubDate>Fri, 06 Feb 2026 00:00:00 -0800</pubDate>
         <dc:date>2026-02-06T12:00:00-08:00</dc:date>
         <source url="https://onlinelibrary.wiley.com/journal/20426984?af=R">Wiley-Online-Library: International Forum of Allergy &amp; Rhinology: Table of Contents</source>
         <prism:coverDate/>
         <prism:coverDisplayDate/>
         <guid isPermaLink="false">10.1002/alr.70114</guid>
         <title>Rationale of New Grading System: Central Compartment Atopic Disease</title>
         <description>International Forum of Allergy &amp;amp;Rhinology, EarlyView. </description>
         <dc:description>
ABSTRACT

Background
Central compartment atopic disease (CCAD) has recently been recognized as a distinct phenotype within the spectrum of type 2–dominant chronic rhinosinusitis (CRS). Although international guidelines highlight polypoid changes in the central nasal cavity, standardized diagnostic and classification criteria are still lacking. This study aims to develop and internally validate a consensus‐based classification system through expert agreement.


Methods
A two‐round modified Delphi study was conducted with 10 international rhinology experts. Participants evaluated the need for a specific grading framework, the relative diagnostic value of nasal endoscopy versus radiology, and the clarity and applicability of the proposed criteria (Grades 0–IV). Six representative endoscopic and radiologic cases were used in each round to assess interpretive accuracy and interobserver agreement. Consensus was predefined as ≥ 80% of ratings in the top two categories (4–5) on a 5‐point Likert scale.


Results
Eighty percent of experts identified nasal endoscopy as the primary diagnostic tool in the first Delphi round. The interpretive accuracy of the preliminary grading system was high, with all panelists correctly recognizing the proposed distinctions. Interobserver agreement was substantial (κ = 0.72). In the second round, refined definitions improved overall consensus and reproducibility. Endoscopy was reaffirmed as the cornerstone of diagnosis, while radiology played a complementary role. Diagnostic clarity and agreement increased, reaching κ = 0.80.


Conclusion
The consensus process confirmed nasal endoscopy as the key diagnostic method for CCAD, supported by substantial interobserver reproducibility. The refined definitions improved clarity and agreement, facilitating differentiation from other CRS phenotypes and establishing a reliable framework for future research.

</dc:description>
         <content:encoded>
&lt;h2&gt;ABSTRACT&lt;/h2&gt;
&lt;h2&gt;Background&lt;/h2&gt;
&lt;p&gt;Central compartment atopic disease (CCAD) has recently been recognized as a distinct phenotype within the spectrum of type 2–dominant chronic rhinosinusitis (CRS). Although international guidelines highlight polypoid changes in the central nasal cavity, standardized diagnostic and classification criteria are still lacking. This study aims to develop and internally validate a consensus-based classification system through expert agreement.&lt;/p&gt;
&lt;h2&gt;Methods&lt;/h2&gt;
&lt;p&gt;A two-round modified Delphi study was conducted with 10 international rhinology experts. Participants evaluated the need for a specific grading framework, the relative diagnostic value of nasal endoscopy versus radiology, and the clarity and applicability of the proposed criteria (Grades 0–IV). Six representative endoscopic and radiologic cases were used in each round to assess interpretive accuracy and interobserver agreement. Consensus was predefined as ≥ 80% of ratings in the top two categories (4–5) on a 5-point Likert scale.&lt;/p&gt;
&lt;h2&gt;Results&lt;/h2&gt;
&lt;p&gt;Eighty percent of experts identified nasal endoscopy as the primary diagnostic tool in the first Delphi round. The interpretive accuracy of the preliminary grading system was high, with all panelists correctly recognizing the proposed distinctions. Interobserver agreement was substantial (&lt;i&gt;κ&lt;/i&gt; = 0.72). In the second round, refined definitions improved overall consensus and reproducibility. Endoscopy was reaffirmed as the cornerstone of diagnosis, while radiology played a complementary role. Diagnostic clarity and agreement increased, reaching &lt;i&gt;κ&lt;/i&gt; = 0.80.&lt;/p&gt;
&lt;h2&gt;Conclusion&lt;/h2&gt;
&lt;p&gt;The consensus process confirmed nasal endoscopy as the key diagnostic method for CCAD, supported by substantial interobserver reproducibility. The refined definitions improved clarity and agreement, facilitating differentiation from other CRS phenotypes and establishing a reliable framework for future research.&lt;/p&gt;</content:encoded>
         <dc:creator>
Ramón Moreno‐Luna, 
Carmen Palma‐Martínez, 
Serafin Sánchez‐Gómez, 
Isam Alobid, 
Daniel Martin‐Jimenez, 
José Miguel Villacampa‐Aubá, 
Christian Calvo‐Henríquez, 
Alfonso Del Cuvillo, 
Alfonso Santamaría‐Gadea, 
Jaime González‐García, 
Richard J. Harvey, 
John M. DelGaudio
</dc:creator>
         <category>ORIGINAL ARTICLE</category>
         <dc:title>Rationale of New Grading System: Central Compartment Atopic Disease</dc:title>
         <dc:identifier>10.1002/alr.70114</dc:identifier>
         <prism:publicationName>International Forum of Allergy &amp; Rhinology</prism:publicationName>
         <prism:doi>10.1002/alr.70114</prism:doi>
         <prism:url>https://onlinelibrary.wiley.com/doi/10.1002/alr.70114?af=R</prism:url>
         <prism:section>ORIGINAL ARTICLE</prism:section>
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