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      <title>Cancer Test copy</title>
      <description>Pipes Output</description>
      <link>http://pipes.yahoo.com/pipes/pipe.info?_id=dc3a835959a1a32841aee8e6ae85f2ad</link>
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      <pubDate>Thu, 01 Oct 2015 00:12:34 +0000</pubDate>
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      <item>
         <title>Concept-elicitation phase for the development of the pediatric patient-reported outcome version of the Common Terminology Criteria for Adverse Events</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29702</link>
         <description>BACKGROUND
Symptoms arising from disease or treatment are subjective experiences. Insight into pediatric oncology treatment side effects or symptoms is ideally obtained from direct inquiry to the ill child. A concept-elicitation phase in a patient-reported outcome (PRO) instrument design provides an opportunity to elicit children's voices to shape cancer symptom selection and terminology.


METHODS
Through semistructured, one-on-one, voice-recorded interviews, symptom data were collected from 96 children with cancer between the ages of 7 and 20 years who were undergoing oncologic treatment at 7 pediatric oncology sites in the United States and Canada.


RESULTS
The mean number of symptoms reported per child over the prior 7 days was 1.49 (range, 0-7; median, 1; standard deviation, 1.56). The most common symptoms across all age groups were tiredness or fatigue, nausea or vomiting, aches or pains, and weakness. There was not a statistically significant correlation between self-reported wellness and the number of reported symptoms (r = –0.156, n = 65, P = .215) or the number of symptoms reported by age group or diagnosis type. Forty participants reported experiencing a change in their body in the past week, with one-third of these changes unanticipated. Only through direct questions about feelings were emotional symptoms revealed because 90.6% of interviewees who discussed feelings (48 of 53) did so only in the context of direct questioning on feelings. Adolescents were more likely than younger children to discuss feelings as part of the interview.


CONCLUSIONS
Concept elicitation from children and adolescents has the potential to enable researchers to develop age-appropriate, accurately representative PRO measures. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Wed, 30 Sep 2015 15:31:26 +0000</pubDate>
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      <item>
         <title>Defining the role of radiofrequency ablation and stereotactic ablative radiotherapy in patients with high-risk, early-stage non-small cell lung cancer</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29698</link>
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         <pubDate>Wed, 30 Sep 2015 08:46:25 +0000</pubDate>
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      <item>
         <title>Reply to defining the role of radiofrequency ablation and stereotactic ablative radiotherapy in patients with high-risk, early-stage non-small cell lung cancer</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29699</link>
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         <pubDate>Wed, 30 Sep 2015 08:46:04 +0000</pubDate>
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      </item>
      <item>
         <title>The Angelina effect revisited: Exploring a media-related impact on public awareness</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29461</link>
         <description>BACKGROUND
In 2013, Angelina Jolie's double mastectomy and publication of her personal treatment choice for BRCA1 positivity generated considerable media attention. To the authors’ knowledge, the current study is the first prospective survey conducted among the general public to measure a quantifiable media-related effect on public awareness.


METHODS
The authors analyzed the changes in the general public's awareness of reconstructive options in breast cancer among 2 female population-matched cohorts aged 18 to 65 years (1000 participants in each cohort) before (March 2013; poll 1) and after (June 2013; poll 2) the announcement of Ms. Jolie's mastectomy in May 2013.


RESULTS
There was an observed increase in public awareness: significantly more women from poll 2 were aware of reconstructive breast surgery being possible after breast cancer-related mastectomy, notably with regard to autologous tissue and single-stage reconstructions. Approximately 20% of the women in poll 2 (205 women) indicated that media coverage regarding Ms. Jolie affected their interest in breast cancer. A question that was exclusive to poll 2 revealed a preference for autologous (66.2%) versus implant-based (8.2%) reconstructions, with the remainder indicating no preference (25.6%). None of the stratification variables were found to be associated with the above findings.


CONCLUSIONS
To the best of the authors’ knowledge, this is the first prospective study to demonstrate a statistically significant impact of a celebrity announcement on public awareness regarding breast cancer treatment. The results underscore the importance of a media-related impact for professionals in the health care sector, which can serve as a tipping point for raising awareness and improving knowledge concerning a specific disease among the general public. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Mon, 28 Sep 2015 07:47:54 +0000</pubDate>
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      <item>
         <title>Specialized survivor clinic attendance is associated with decreased rates of emergency department visits in adult survivors of childhood cancer</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29679</link>
         <description>BACKGROUND
Survivors of childhood cancer are at considerable risk of experiencing treatment-related adverse health outcomes. To provide survivors with specialized care focused on these risks during adulthood, the government of Ontario funded a provincial network of specialized survivor clinics in 1999. The aim of this study was to determine whether prior attendance at survivor clinics by adult survivors of childhood cancer was associated with rates of emergency department (ED) visits.


METHODS
This was a population-based, retrospective cohort study using multiple linked administrative health databases. The cohort consisted of all adult survivors of childhood cancer diagnosed between January 1, 1986 and December 31, 2005 in Ontario, Canada. A recurrent event regression model was used to evaluate the association between prior attendance at survivor clinics and the rate of ED visits; adjustments were made for individual, demographic, treatment, and provider characteristics.


RESULTS
The study consisted of 3912 adult survivors of childhood cancer. Individuals who had at least 1 prior visit to a survivor clinic had a 19% decreased rate of ED visits in comparison with individuals who had not visited a survivor clinic (adjusted relative rate, 0.81; 95% confidence interval, 0.78-0.85). Each additional prior visit to a survivor clinic was associated with a 5% decrease in the rate of ED visits (adjusted relative rate, 0.95; 95% confidence interval, 0.93-0.96). These results were independent of whether or not survivors received care from a primary care physician.


CONCLUSIONS
Attendance at a specialized survivor clinic was significantly associated with decreased ED visits among adult survivors of childhood cancer. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Fri, 25 Sep 2015 08:16:03 +0000</pubDate>
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      <item>
         <title>Specialty care for adult survivors of childhood cancer</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29683</link>
         <description>As adult survivors of childhood cancer age, they are at risk for serious morbidity related to their cancer therapy. How best to manage this high-risk population, which is often unaware of the risks and is followed by primary care clinicians unfamiliar with cancer therapy, remains understudied. In an intriguing study, Sutradhar et al report that attendance at a specialized survivor clinic results in fewer emergency department visits.</description>
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         <pubDate>Fri, 25 Sep 2015 08:15:37 +0000</pubDate>
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      <item>
         <title>Case-linked analysis of clinical trial enrollment among adolescents and young adults at a National Cancer Institute-Designated comprehensive cancer center</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29669</link>
         <description>BACKGROUND
Poor accrual to cancer clinical trials may contribute to the lower improvement in survival observed for adolescents and young adults (AYAs) (those aged 15-39 years) with cancer. This has been difficult to quantify without reliable mechanisms to link incident cases with study enrollments. Using unique resources available at their National Cancer Institute-designated comprehensive cancer center, the authors compared the percentage of AYAs, children, and older adults enrolled onto cancer clinical trials and determined predictors of enrollment.


METHODS
Patients diagnosed with cancer from January 2008 through December 2012 at 1 pediatric and 2 adult University of Southern California hospitals were identified through the California Cancer Registry and individually linked to institutional trial enrollment databases. The availability of clinical trials was assessed.


RESULTS
Across the center, the enrollment percentage for AYAs (6%) was equal to that of older adults (6%), but was less than that for children (22%) (P &amp;lt; .01). Within the children's hospital, the AYA enrollment percentage was also less than that for children (15% vs 23%, respectively; P&amp;lt;.01). On multivariate analysis, diagnosis and site of care were found to be predictive of AYA enrollment onto therapeutic and nontherapeutic studies. Hispanic and Asian/Pacific Islander individuals were more likely to enroll onto nontherapeutic studies compared with non-Hispanic whites, but no racial/ethnic difference was observed for therapeutic studies.


CONCLUSIONS
In the current study, the percentages of AYAs and older adults enrolled onto therapeutic trials were low but similar. Diagnosis, site of care, and race/ethnicity appear to be predictive of enrollment. Prospective mechanisms must be instituted to capture reasons for nonenrollment of AYAs and develop corrective interventions. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Tue, 22 Sep 2015 10:32:54 +0000</pubDate>
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      </item>
      <item>
         <title>Antiviral therapy and hepatocellular carcinogenesis</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29696</link>
         <guid isPermaLink="false"></guid>
         <pubDate>Fri, 18 Sep 2015 11:33:15 +0000</pubDate>
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      </item>
      <item>
         <title>Reply to antiviral therapy and hepatocellular carcinogenesis</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29694</link>
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         <pubDate>Fri, 18 Sep 2015 11:32:52 +0000</pubDate>
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      <item>
         <title>Minimal clinically important difference and Edmonton Symptom Assessment Scale</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29695</link>
         <guid isPermaLink="false"></guid>
         <pubDate>Fri, 18 Sep 2015 11:30:52 +0000</pubDate>
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      </item>
      <item>
         <title>Reply to minimal clinically important difference and Edmonton Symptom Assessment Scale</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29690</link>
         <guid isPermaLink="false"></guid>
         <pubDate>Fri, 18 Sep 2015 11:30:06 +0000</pubDate>
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      <item>
         <title>The effect of Paget disease on axillary lymph node metastases and survival in invasive ductal carcinoma</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29687</link>
         <description>BACKGROUND
The objective of this study was to examine the effect of Paget disease (PD) on axillary lymph node metastases and survival in patients who had concomitant invasive ductal carcinoma (PD-IDC).


METHODS
The Surveillance, Epidemiology, and End Results (SEER) database was used to identify women who were diagnosed with PD-IDC from 2000 to 2011, comparing baseline demographic and tumor characteristics with those who were diagnosed with IDC alone during the same period. Multivariable logistic regression was used to examine the association of PD-IDC with axillary lymph node metastasis, and breast cancer-specific survival and overall survival were compared between the PD-IDC and IDC groups using the Kaplan-Meier method and Cox proportional hazards regression.


RESULTS
The study cohort included 1102 patients with PD-IDC and 302,242 controls with IDC alone. PD-IDC tumors were more likely to be centrally located (26.9% vs 5.5%; P &amp;lt; .001), high grade (63.5% vs 40.3%; P &amp;lt; .001), &amp;gt;2 cm in greatest dimension (47.1% vs 35.7%; P &amp;lt; .001), and estrogen/progesterone receptor-negative (45.2% vs 22.1%; P &amp;lt; .001). In adjusted analyses, patients with PD-IDC had higher odds of axillary lymph node metastasis (odds ratio, 1.83; P &amp;lt; .001). The unadjusted 10-year breast cancer-specific and overall survival rates were lower for the PD-IDC group compared with the IDC-alone group, although, after adjusting for disease stage, tumor characteristics, and local therapy, no significant differences in mortality risk were observed between the 2 groups (hazard ratio, 0.91; P = .24).


CONCLUSIONS
PD-IDC is associated with an increased risk of axillary lymph node metastasis, but not with inferior survival, compared with IDC alone after adjustment for other disease factors. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Wed, 16 Sep 2015 10:18:25 +0000</pubDate>
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      <item>
         <title>Outcomes of postchemotherapy retroperitoneal lymph node dissection following high-dose chemotherapy with stem cell transplantation</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29678</link>
         <description>BACKGROUND
Characterizing the role of postchemotherapy retroperitoneal lymph node dissection (PC-RPLND) after high-dose chemotherapy (HDCT) has been limited by small sample sizes. This study reports on survival after HDCT with stem cell support and PC-RPLND as well as histologic findings in the retroperitoneum.


METHODS
The prospectively maintained testicular cancer database of Indiana University was queried for patients receiving HDCT with stem cell transplantation before PC-RPLND. The cause and date of death were obtained through patient chart review and contact with referring physicians. The Kaplan-Meier method was used to evaluate overall survival (OS). The log-rank test was used for tests of significance. A multivariate, backward, stepwise Cox regression model was built to evaluate predictors of overall mortality.


RESULTS
A total of 92 patients were included in the study. In the entire cohort, the retroperitoneal (RP) histology findings at the time of PC-RPLND were necrosis (26%), teratoma (34%), and cancer (38%). Sixty-six patients (72%) harbored either a teratoma or active cancer in the RP specimen at PC-RPLND. The median follow-up for the entire cohort was 80.6 months. A total of 28 patients (30%) died during follow-up. The 5-year OS rate of the entire cohort was 70%. The most significant predictor of death was PC-RPLND performed in the desperation setting with elevated markers.


CONCLUSIONS
Despite these patients being heavily pretreated with multiple cycles of chemotherapy, including HDCT, approximately three-fourths were found to have a teratoma and/or active cancer in the retroperitoneum. This underscores the importance of PC-RPLND for rendering patients free of disease and providing a potential for cure. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Tue, 15 Sep 2015 13:13:32 +0000</pubDate>
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      <item>
         <title>Cost-effectiveness analysis of neurocognitive-sparing treatments for brain metastases</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29642</link>
         <description>BACKGROUND
Decisions regarding how to treat patients who have 1 to 3 brain metastases require important tradeoffs between controlling recurrences, side effects, and costs. In this analysis, the authors compared novel treatments versus usual care to determine the incremental cost-effectiveness ratio from a payer's (Medicare) perspective.


METHODS
Cost-effectiveness was evaluated using a microsimulation of a Markov model for 60 one-month cycles. The model used 4 simulated cohorts of patients aged 65 years with 1 to 3 brain metastases. The 4 cohorts had a median survival of 3, 6, 12, and 24 months to test the sensitivity of the model to different prognoses. The treatment alternatives evaluated included stereotactic radiosurgery (SRS) with 3 variants of salvage after recurrence (whole-brain radiotherapy [WBRT], hippocampal avoidance WBRT [HA-WBRT], SRS plus WBRT, and SRS plus HA-WBRT). The findings were tested for robustness using probabilistic and deterministic sensitivity analyses.


RESULTS
Traditional radiation therapies remained cost-effective for patients in the 3-month and 6-month cohorts. In the cohorts with longer median survival, HA-WBRT and SRS plus HA-WBRT became cost-effective relative to traditional treatments. When the treatments that involved HA-WBRT were excluded, either SRS alone or SRS plus WBRT was cost-effective relative to WBRT alone. The deterministic and probabilistic sensitivity analyses confirmed the robustness of these results.


CONCLUSIONS
HA-WBRT and SRS plus HA-WBRT were cost-effective for 2 of the 4 cohorts, demonstrating the value of controlling late brain toxicity with this novel therapy. Cost-effectiveness depended on patient life expectancy. SRS was cost-effective in the cohorts with short prognoses (3 and 6 months), whereas HA-WBRT and SRS plus HA-WBRT were cost-effective in the cohorts with longer prognoses (12 and 24 months). Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Tue, 15 Sep 2015 13:13:11 +0000</pubDate>
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         <title>Pretreatment depression as a prognostic indicator of survival and nutritional status in patients with head and neck cancer</title>
         <link>http://onlinelibrary.wiley.com/resolve/doi?DOI=10.1002%2Fcncr.29693</link>
         <description>BACKGROUND
The emotional status of cancer patients is associated with disease course and treatment outcomes. In this study, the authors evaluated associations between the presence of pretreatment depression and pretreatment quality of life (QOL), nutritional status, and survival outcomes in patients with head and neck squamous cell carcinoma (HNSCC).


METHODS
For this prospective study, 241 patients with previously untreated HNSCC who underwent curative treatments were enrolled. Patients completed the Beck Depression Inventory (BDI)-II, the European Organization for Research and Treatment of Cancer (EORTC) 30-item Core QOL Questionnaire (QLQ-C30), and the EORTC QLQ Head and Neck Cancer module (QLQ-H&amp;N35). EORTC QLQ scores were compared between depressive and nondepressive patients, as determined according to pretreatment BDI-II scores ≥14 and &amp;lt;14, respectively. Univariate and multivariate analyses were performed to assess whether the presence of depression was associated with overall survival, disease-free survival (DFS), or posttreatment changes in nutritional status and laboratory data.


RESULTS
Pretreatment depression was present in 60 patients (24.9%). In depressive and nondepressive patients, the 3-year overall survival rates were 70.8% and 82.7%, respectively (P = .045), and the 3-year DFS rates were 63.5% and 79.1%, respectively (P = .015). After controlling for clinical factors, the presence of depression was predictive of 3-year DFS (P = .032). EORTC QLQ-C30 and QLQ-HN35 scores on all items except feeding tube, nutritional supplement, and problem with mouth opening differed between depressive and nondepressive patients (P &amp;lt; .05). Depressive patients had lower pretreatment serum albumin levels than nondepressive patients (P &amp;lt; .05).


CONCLUSIONS
There was a significant correlation between pretreatment depression and pretreatment QOL, nutritional status, and survival outcomes in patients with HNSCC. Cancer 2015. © 2015 American Cancer Society.</description>
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         <pubDate>Tue, 15 Sep 2015 13:12:44 +0000</pubDate>
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