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<title><![CDATA[Andrea's Buddy Blog]]></title>
<link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckPersonaPage=PersonaBlog&amp;sid=sitelife.wusa9.com</link>
<description><![CDATA[For anyone who is or has battled breast cancer and for people who want to live life to the fullest..]]></description>
<copyright><![CDATA[Copyright 2012, Asbury Park Press.com on behalf of AndreaRoane]]></copyright>
<lastBuildDate>Mon, 12 Dec 2011 14:10:00 GMT</lastBuildDate>
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        <title><![CDATA[A Well Deserved Honor For the First Permanent Director of the Office of Research on Women's Health at NIH]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a3662da61-0688-42fe-9dbe-95f11ff5d986&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Mon, 12 Dec 2011 14:10:00 GMT</pubDate>
        <description><![CDATA[<h1 class="title">Dr. Vivian W. Pinn to receive inaugural Bernadine Healy Award</h1><h2 class="subtitle">Given at 20th Annual Congress on Women's Health</h2><p><table border="0" cellspacing="0" cellpadding="0" width="218" align="right"><tbody><tr><td colspan="5"><img border="0" alt="" width="1" height="10" src="http://www.eurekalert.org/images/clear.gif" /></td></tr><tr><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2" height="4" valign="top" width="4" align="left"><img border="0" alt="" width="4" height="4" src="http://www.eurekalert.org/images/corner_tl.jpg" /></td><td bgcolor="#f2f2f2" height="4" width="210"><img border="0" alt="" width="1" height="10" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2" height="4" valign="top" width="4" align="right"><img border="0" alt="" width="4" height="4" src="http://www.eurekalert.org/images/corner_tr.jpg" /></td><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td></tr><tr><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2"><img border="0" alt="" width="4" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2"><center><a target="_self" href="http://www.eurekalert.org/multimedia/pub/38932.php?from=200602"><img border="0" alt="" src="http://www.eurekalert.org/multimedia/pub/rel/38932_rel.jpg" /></a> </center><p><a target="_self" href="http://www.eurekalert.org/multimedia/pub/38932.php?from=200602"><img border="0" alt="" src="http://www.eurekalert.org/images/eutube/icon_image_tiny.gif" /><font color="#2c56ac"> </font><span class="imagecaption" style="color:black;"><b><font size="1">IMAGE:</font></b></span></a> <font size="1"><span class="imagecaption">This is the design for the 20th Annual Congress on Women&rsquo;s Health.</span><br /></font></p><center><span class="imagecaption"><a target="_self" href="http://www.eurekalert.org/multimedia/pub/38932.php?from=200602"><font color="#2c56ac" size="1">Click here for more information.</font></a></span> </center><p>&nbsp;</p></td><td bgcolor="#f2f2f2"><img border="0" alt="" width="4" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td></tr><tr><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2" height="4" valign="bottom" width="4" align="left"><img border="0" alt="" width="4" height="4" src="http://www.eurekalert.org/images/corner_bl.jpg" /></td><td bgcolor="#f2f2f2" height="4" width="202"><img border="0" alt="" width="1" height="10" src="http://www.eurekalert.org/images/clear.gif" /></td><td bgcolor="#f2f2f2" height="4" valign="bottom" width="4" align="right"><img border="0" alt="" width="4" height="4" src="http://www.eurekalert.org/images/corner_br.jpg" /></td><td><img border="0" alt="" width="8" height="1" src="http://www.eurekalert.org/images/clear.gif" /></td></tr><tr><td colspan="5"><img border="0" alt="" width="1" height="10" src="http://www.eurekalert.org/images/clear.gif" /></td></tr></tbody></table></p><p>New Rochelle, NY -- Vivian W. Pinn, MD will be awarded the inaugural Bernadine Healy Award, to be presented at the 20th Annual Congress on Women's Health, March 16-18, 2012 in Washington, DC. Physicians, nurses, and allied healthcare providers from across the country will gather at the Congress to learn practical, clinical information, cutting-edge therapeutic protocols, advances in diagnosis and management, and innovative translational research advances that impact women's health care. Complete information is available on the Congress website.</p><p>The Bernadine Healy Award was created in honor of the work and memory of Bernadine Healy, MD, former National Institutes of Health (NIH) Director, Founding Editor of Journal of Women's Health, and a renowned advocate for women's health. Through her tireless passion and leadership, Dr. Healy encouraged discourse and exchange of information among health care professionals with the ultimate goal of promoting women's health as a high national priority.</p><p>Dr. Pinn recently retired as the first permanent director of the Office of Research on Women's Health (ORWH) at NIH, and has long been active in efforts to improve health and career opportunities for women and minorities and to raise awareness in the scientific community about the importance of sex and gender factors in basic science, clinical research, and health care. She most recently spearheaded a national effort to reexamine priorities for the women's health agenda for the 21st Century, involving advocates, scientists, policy makers, educators, and health care providers in a series of scientific meetings across the country that ultimately informed the ORWH's new strategic plan.</p><p>"There is no better way to honor Dr. Healy's memory than to recognize the contributions of Vivian Pinn, a truly visionary leader who has advanced women's health immeasurably," says Congress Co-Chair Wendy S. Klein, MD, Senior Deputy Director Emeritus of the VCU Institute for Women's Health and Deputy Editor of <i>Journal of Women's Health</i>.</p><p>The 20th Annual Congress on Women's Health is hosted by the VCU Institute for Women's Health and Journal of Women's Health, in collaboration with NIH Office of Research on Women's Health and National Cancer Institute. Dr. Klein and Co-Chair Susan G. Kornstein, MD, Executive Director of the VCU Institute for Women's Health and Editor-in-Chief of Journal of Women's Health, will bring together outstanding faculty of the highest caliber for an array of informative sessions focusing on the most clinically relevant topics in women's health including cardiology, oncology, endocrinology, menopause, infectious disease, reproductive health, bone health, psychiatry, and common clinical conditions.</p><p>The Congress will offer up to 24.5 credit hours for physicians, nurse practitioners, nurses, family physicians, and allied health care professionals. This activity is jointly sponsored by Global Education Group and Institute for Professional Education.</p>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Study finds side effects, complications, mastectomy more likely after partial breast irradiation]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a8212cb20-89e5-4e1b-af55-72b8d3b5d42e&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Tue, 06 Dec 2011 23:31:00 GMT</pubDate>
        <description><![CDATA[<p>San Antonio, TX - Accelerated partial breast irradiation (APBI) brachytherapy, the localized form of radiation therapy growing increasingly popular as a treatment choice for women with early-stage breast cancer, is associated with higher rate of later mastectomy, increased radiation-related toxicities and post-operative complications, compared to traditional whole breast irradiation (WBI), according to researchers from The University of Texas MD Anderson Cancer Center.</p><p>The retrospective study was presented in the CTRC-AACR San Antonio Breast Cancer Symposium's press briefing by Benjamin Smith, M.D., assistant professor in the Department of Radiation Oncology, and in the meeting's scientific session by Grace Smith, M.D., Ph.D., a resident in MD Anderson's Department of Radiation Oncology and the study's first author.</p><p>"Our study compared the two radiation therapy techniques available to women with early-stage breast cancer. We found that women treated with accelerated partial breast irradiation therapy have a two-fold increased risk for subsequent mastectomy, most likely because of tumor recurrence or local complications, as well as an increased risk for post-operative and radiation-related complications," said Ben Smith, the study's senior author.</p><p>There are numerous types of APBI; the MD Anderson study only looked at the brachytherapy technique, in which a form of radiation treatment involving insertion of a catheter containing a radioactive source to kill breast cancer cells that may remain after lumpectomy surgery. A specialized catheter is surgically inserted into the cavity left behind after tumor removal. APBI brachytherapy is performed a few weeks after a lumpectomy, twice daily over a course of five to seven days.</p><p>APBI brachytherapy has grown in popularity over the past decade, since earlier studies showed generally low cancer recurrence rates, though most prior studies have not directly compared the outcomes of APBI brachytherapy to traditional radiation therapy, explained Ben Smith.</p><p>The first commercially-available single catheter to deliver partial breast irradiation was approved by the FDA in 2002, escalating APBI's use, said Ben Smith.</p><p>The MD Anderson study was based on analysis of claim forms filed by 130,535 Medicare beneficiaries nationwide, who were diagnosed with cancer between 2000 and 2007.</p><p>"In our study of Medicare patients, we found a consistent increase in APBI brachytherapy, from less than 1 percent in 2000 to 13 percent in 2007. It's our guess that this trend has continued," said Smith.</p><p>There are benefits to the practicality APBI offers women, noted Ben Smith.</p><p>"For whole breast irradiation, the standard treatment time is between five and seven weeks, but studies have shown that some women experience delays or have obstacles completing their course of radiation. Treatment delays and incompletion are known to increase the risk of cancer recurrence in the breast. APBI brachytherapy is attractive because it has the potential to address those issues, because treatment only lasts one week."</p><p>However, it's also an invasive procedure with the greater potential for side-effects that are not associated with a non-invasive therapy, such as WBI, noted Smith.</p><p>For the retrospective population-based study, the MD Anderson team used Medicare claims to examine the treatment history of 130,535 women age 66 and older diagnosed with early-stage, invasive breast cancer between 2000 and 2007. All of the women were treated with breast-conserving surgery followed by either APBI, delivered by brachytherapy, or traditional radiation therapy.</p><p>The researchers analyzed for effectiveness of radiation (defined as the need for a later mastectomy), post-operative complications (infectious and non-infectious), and post-radiation complications (breast pain, fat necrosis and rib fracture).</p><p>At five years, the incidence of mastectomy was statistically significantly higher in the APBI brachytherapy-treatment group compared to that of the WBI, 4 percent and 2.2 percent, respectively. APBI brachytherapy was also found to be associated with a higher incidence of acute and late toxicities, compared to those of WBI - infectious complications, 16 and 10 percent, respectively; non-infectious complications, 16 percent and 8 percent, respectively; - and post-radiation complications - five-year incidence of rib fracture, 4 and 4 percent, respectively; fat necrosis, 9 and 4 percent, respectively; and breast pain, 15 percent and 12 percent, respectively.</p><p>The researchers note the study's limits, including that it was not randomized, the relatively-short follow up of patients and limited details regarding tumor characteristics were available.</p><p>Given the findings, communication between the patient and her physician is paramount so that a woman with breast cancer can make an informed, personalized decision, said Thomas A. Buchholz, M.D., professor and head of the Division of Radiation Oncology at MD Anderson.</p><p>"This is a very important, well-designed study in a large cohort of patients and provides the first comparison of these two popular radiation techniques after breast-conserving surgery," said Buchholz, also an author on the study. "It's important to note that in both groups, we found a relatively low risk of recurrence. Still, we have a responsibility to discuss potential risks and benefits with our patients, while we await definitive results from randomized trials."</p><p>National randomized trials comparing APBI brachytherapy to WBI are ongoing. MD Anderson will continue offering APBI to interested patients in the context of ongoing institutional and multi-institutional clinical protocols, says Buchholz.</p><p>&nbsp;</p><div align="center">###</div>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[The New Achilles Heel In Breast Cancer]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a3c087fe2-96d7-4672-b187-3c6a631308c1&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Thu, 01 Dec 2011 14:03:00 GMT</pubDate>
        <description><![CDATA[<h2 class="subtitle">Off-patent generic drug Metformin prevents cancer cells from using their mitochondria to grow and spread throughout the body</h2><p><table border="0" cellspacing="0" cellpadding="0" width="218" align="right"><tbody><tr><td colspan="5"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="1" height="10" /></td></tr><tr><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td><td bgcolor="#f2f2f2" height="4" valign="top" width="4" align="left"><img border="0" alt="" src="http://www.eurekalert.org/images/corner_tl.jpg" width="4" height="4" /></td><td bgcolor="#f2f2f2" height="4" width="210"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="1" height="10" /></td><td bgcolor="#f2f2f2" height="4" valign="top" width="4" align="right"><img border="0" alt="" src="http://www.eurekalert.org/images/corner_tr.jpg" width="4" height="4" /></td><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td></tr><tr><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td><td bgcolor="#f2f2f2"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="4" height="1" /></td><td bgcolor="#f2f2f2"><center><a href="http://www.eurekalert.org/multimedia/emb/38471.php?from=199744" target="_self"><img border="0" src="http://www.eurekalert.org/multimedia/emb/rel/38471_rel.jpg" alt="" /></a> </center><p><a href="http://www.eurekalert.org/multimedia/emb/38471.php?from=199744" target="_self"><img border="0" src="http://www.eurekalert.org/images/eutube/icon_image_tiny.gif" alt="" /><font color="#2c56ac"> </font><span class="imagecaption" style="color:black;"><b><font size="1">IMAGE:</font></b></span></a> <font size="1"><span class="imagecaption">This is Michael P. Lisanti, M.D., Ph.D., Professor and Chair of Stem Cell Biology &amp; Regenerative Medicine at Thomas Jefferson University.</span><br /></font></p><center><span class="imagecaption"><a href="http://www.eurekalert.org/multimedia/emb/38471.php?from=199744" target="_self"><font color="#2c56ac" size="1">Click here for more information.</font></a></span> </center><p>&nbsp;</p></td><td bgcolor="#f2f2f2"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="4" height="1" /></td><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td></tr><tr><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td><td bgcolor="#f2f2f2" height="4" valign="bottom" width="4" align="left"><img border="0" alt="" src="http://www.eurekalert.org/images/corner_bl.jpg" width="4" height="4" /></td><td bgcolor="#f2f2f2" height="4" width="202"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="1" height="10" /></td><td bgcolor="#f2f2f2" height="4" valign="bottom" width="4" align="right"><img border="0" alt="" src="http://www.eurekalert.org/images/corner_br.jpg" width="4" height="4" /></td><td><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="8" height="1" /></td></tr><tr><td colspan="5"><img border="0" alt="" src="http://www.eurekalert.org/images/clear.gif" width="1" height="10" /></td></tr></tbody></table></p><p>PHILADELPHIA -- Researchers at the <a href="http://www.kimmelcancercenter.org/"><font color="#2c56ac">Kimmel Cancer Center at Jefferson</font></a> have identified cancer cell mitochondria as the unsuspecting powerhouse and "Achilles' heel" of tumor growth, opening up the door for new therapeutic targets in breast cancer and other tumor types.</p><p>Reporting in the online Dec.1 issue of <i>Cell Cycle</i>, <a href="http://www.jefferson.edu/cancerbiology/faculty_profile.cfm?key=mpl001"><font color="#2c56ac">Michael P. Lisanti, M.D., Ph.D., Professor and Chair of Stem Cell Biology &amp; Regenerative Medicine</font></a> at <a href="http://www.jefferson.edu/"><font color="#2c56ac">Thomas Jefferson University</font></a>, and colleagues provide the first in vivo evidence that breast cancer cells perform enhanced mitochondrial oxidative phosphorylation (OXPHOS) to produce high amounts of energy.</p><p>"We and others have now shown that cancer is a 'parasitic disease' that steals energy from the host -- your body," Dr. Lisanti said, "but this is the first time we've shown in human breast tissue that cancer cell mitochondria are calling the shots and could ultimately be manipulated in our favor."</p><p>Mitochondria are the energy-producing power-plants in normal cells. However, cancer cells have amplified this energy-producing mechanism, with at least five times as much energy-producing capacity, compared with normal cells. Simply put, mitochondria are the powerhouse of cancer cells and they fuel tumor growth and metastasis.</p><p>The research presented in the study further supports the idea that blocking this activity with a mitochondrial inhibitor -- for instance, an off-patent generic drug used to treat diabetes known as Metformin -- can reverse tumor growth and chemotherapy resistance. This new concept could radically change how we treat cancer patients, and stimulate new metabolic strategies for cancer prevention and therapy.</p><p><b>Investigating the Powerhouse</b></p><p>Whether cancer cells have functional mitochondria has been a hotly debated topic for the past 85 years. It was argued that cancer cells don't use mitochondria, but instead use glycolysis exclusively; this is known as the Warburg Effect. But researchers at the Jefferson's KCC have shown that this inefficient method of producing energy actually takes place in the surrounding host stromal cells, rather then in epithelial cancer cells. This process then provides abundant mitochondrial fuel for cancer cells. They've coined this the "Reverse Warburg Effect," the opposite or reverse of the existing paradigm.</p><p>To study mitochondria's role directly, the researchers, including co-author and collaborator <a href="http://www.jefferson.edu/cancerbiology/faculty_profile.cfm?key=fxs002"><font color="#2c56ac">Federica Sotgia, Assistant Professor in the Department of Cancer Biology</font></a>, looked at mitochondrial function using COX activity staining in human breast cancer samples. Previously, this simple stain was only applied to muscle tissue, a mitochondrial-rich tissue.</p><p>Researchers found that human breast cancer epithelial cells showed amplified levels of mitochondrial activity. In contrast, adjacent stromal tissues showed little or no mitochondrial oxidative capacity, consistent with the new paradigm. These findings were further validated using a computer-based informatics approach with gene profiles from over 2,000 human breast cancer samples.</p><p>It is now clear that cancer cell mitochondria play a key role in "parasitic" energy transfer between normal fibroblasts and cancer cells, fueling tumor growth and metastasis.</p><p>"We have presented new evidence that cancer cell mitochondria are at the heart of tumor cell growth and metastasis," Dr. Lisanti said. "Metabolically, the drug Metformin prevents cancer cells from using their mitochondria, induces glycolysis and lactate production, and shifts cancer cells toward the conventional 'Warburg Effect'. This effectively starves the cancer cells to death".</p><p><b>Personalized Treatment</b></p><p>Although COX mitochondrial activity staining had never been applied to cancer tissues, it could now be used routinely to distinguish cancer cells from normal cells, and to establish negative margins during cancer surgery. And this is a very cost-effective test, since it has been used routinely for muscle-tissue for over 50 years, but not for cancer diagnosis.</p><p>What's more, it appears that upregulation of mitochondrial activity is a common feature of human breast cancer cells, and is associated with both estrogen receptor positive (ER+) and negative (ER-) disease. Outcome analysis indicated that this mitochondrial gene signature is also associated with an increased risk of tumor cell metastasis, particularly in ER-negative (ER-) patients.</p><p>"Mitochondria are the 'Achilles' heel' of tumor cells," Dr. Lisanti said. "And we believe that targeting mitochondrial metabolism has broad implications for both cancer diagnostics and therapeutics, and could be exploited in the pursuit of personalized cancer medicine."</p>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Updated Canadian Breast Cancer Screening Guidelines Stir Up Old Controversy]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a8b54649c-c479-4dd1-94ea-a5df862ec094&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Mon, 21 Nov 2011 17:01:00 GMT</pubDate>
        <description><![CDATA[<p><b style="mso-bidi-font-weight:normal;"><span style="mso-spacerun:yes;">Canadian Task Force on Preventive Health Care issues updated guidelines&nbsp;<br /><br />New breast cancer screening guidelines for women at average risk of breast cancer, published in CMAJ (Canadian Medical Association Journal) (pre-embargo link only) http://www.cmaj.ca/site/embargo/cmaj110334.pdf, recommend no routine mammography screening for women aged 40-49 and extend the screening interval from every 2 years, which is current clinical practice, to every 2 to 3 years for women aged 50-74. The guidelines also recommend against routine clinical breast exam and breast self-examination in asymptomatic women.<br /><br />The guidelines, aimed at physicians and policy-makers, provide recommendations for mammography, magnetic resonance imaging (MRI), breast self-exams and clinical breast exams by clinicians. They target average-risk women in three age groups (40&#56033;&#57245;, 50&#56033;&#57265; and 70&#56033;&#57270; years) who have not had breast cancer and do not have a family history of breast cancer in a mother, sister or daughter. <br /><br />"As the Guideline on Breast Cancer Screening was last updated in 2001 and breast cancer screening has since become a subject for discussion amongst doctors and patients, the revitalized Canadian Task Force selected breast cancer screening as the topic for its first guideline," said Dr. Marcello Tonelli, Chair of the Task Force on Preventive Health Care and Associate Professor at the University of Alberta, Department of Medicine, in Edmonton, Alberta. "We intend that this Guideline, which reflects the latest scientific evidence in breast cancer screening, be used to guide physicians and their patients regarding the optimum use of mammograms and breast examination."<br /><br />According to the guideline, outcomes of breast cancer screening such as tumour detection and mortality must be put into context of the harms and costs of false&ndash;positive tests, overdiagnosis and overtreatment. False&ndash;positive results can have a significant impact on the emotional well-being of patients and families. They can cause lifestyle disruptions and result in costs to both patients and the health care system. <br /><br />"Providing Canadians with guidelines that reflect the most current scientific evidence is our priority," said Dr. Tonelli. "We encourage every woman to discuss the risks and benefits of screening with their doctor before deciding on the best approach for them."<br /><br />Key recommendations:<br /><br />No routine mammography for women aged 40-49 because the risk of cancer is low in this group while the risk of false&ndash;positive results and overdiagnosis and overtreatment is higher<br /><br />Routine screening with mammography every two to three years for women aged 50-69<br /><br />Routine screening with mammography every two to three years for women aged 70-74<br /><br />No screening of average-risk women using MRI <br /><br />No routine clinical breast exams or breast self-exam to screen for breast cancer.<br /><br />"There was no evidence that screening with mammography reduces the risk of all-cause mortality," state the authors. "Although screening might permit surgery for breast cancer at an earlier stage than diagnosis of clinically evident cancer (thus permitting the use of less invasive procedures for some women), available trial data suggest that the overall risk of mastectomy is significantly increased among recipients of screening compared with women who have not undergone screening."<br /><br />In addition to the full guidelines, one-page information pieces are available for both physicians and patients on the task force website: www.canadiantaskforce.ca<br /><br />The Canadian Task Force on Preventive Health Care is an independent body of 14 primary care and prevention experts. The task force has been established by the Public Health Agency of Canada to develop clinical practice guidelines that support primary care providers in delivering preventive health care. <br /><br />In a related commentary http://www.cmaj.ca/site/embargo/cmaj111721.pdf, Dr. Peter G&oslash;tzsche, Nordic Cochrane Centre, Copenhagen, Denmark, writes, "these guidelines are more balanced and more in accordance with the evidence than any previous recommendations."<br /><br />He states that evidence does not support mammography screening and argues that screening is ineffective and even harmful because diagnosis of cancers that would otherwise be undetected lead to life-shortening treatments and mastectomies.<br /><br />"The main effect of screening is to produce patients with breast cancer from among healthy women who would have remained free of breast disease for the rest of their lives had they not undergone screening," writes Dr. G&oslash;tzsche. <br /><br />"The best method we have to reduce the risk of breast cancer is to stop the screening program," he concludes. "This could reduce the risk by one-third in the screened age group, as the level of overdiagnosis in countries with organized screening programs is about 50%."</span></b></p>]]></description>
        <guid>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a8b54649c-c479-4dd1-94ea-a5df862ec094&amp;sid=sitelife.wusa9.com</guid>
        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Working On New and Better Biomarkers To Improve Early Detection]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3aa78fd67b-5105-421e-825a-e5aa172e1066&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Thu, 17 Nov 2011 09:19:00 GMT</pubDate>
        <description><![CDATA[<p>Tumors can grow for 10 years or longer before currently available blood tests will detect them, a new mathematical model developed by Stanford University School of Medicine scientists indicates. The analysis, which was restricted to ovarian tumors but is broadly applicable across all solid tumor types, will be published online Nov. 16 in Science Translational Medicine.<br /><br />"The study's results can be viewed as both bad and good news," said Sanjiv "Sam" Gambhir, MD, PhD, professor and chair of radiology and the study's senior author. (Sharon Hori, PhD, a postdoctoral scholar in Gambhir's laboratory, is the lead author.)<br /><br />The bad news, Gambhir said, is that by the time a tumor reaches a detectable size using today's available blood tests, it is likely to have metastasized to other areas of the body, making it much more deadly than if it had been caught early on. "The good news is that we have, potentially, 10 or even 20 years to find the tumor before it reaches this size, if only we can improve our blood-based methods of detecting tumors," he said. "We think our mathematical model will help guide attempts to do that."<br /><br />The study advances previous research about the limits of current detection methods. For instance, it is strikingly consistent with a finding reported two years ago by Stanford biochemistry professor Patrick Brown, MD, PhD, that current ovarian cancer tests could not detect tumors early enough to make a significant dent in the mortality rate. There is a push to develop more-sensitive diagnostic tests and find better biomarkers, and Gambhir's new model could be an essential tool in this effort. It for the first time connects the size of a tumor with blood biomarker levels being shed by that tumor.<br /><br />To create their model, Gambhir and Hori used mathematical models originally developed to predict the concentration of drugs injected into the blood as they move in and out of the bloodstream. The investigators linked these to additional models of tumor cell growth.<br /><br />Tumors don't secrete drugs, but they can shed telltale molecules into surrounding tissue, from which those substances, known as biomarkers, diffuse into the blood. Some biomarkers may be made predominantly by tumor cells, while others exclusively by them. Either way, these substances can be measured in the blood as proxies for a tumor.<br /><br />Some biomarkers are in wide use today. One is the well-known PSA, for prostate cancer. Another is CA125, for ovarian cancer. But these and other currently used blood tests for cancer biomarkers weren't specifically developed for early detection, and are generally more effective for relatively noninvasive monitoring of the progress of late-stage tumors or their response to treatment. (Rising blood levels of the substance indicate that the tumor is growing, while declining levels denote possible shrinkage.)<br /><br />Both CA125 and PSA are also produced, albeit in smaller amounts, by healthy tissue, complicating efforts to detect cancer at an early stage when the tumor's output of the biomarker is relatively low.<br /><br />The new mathematical model employs separate equations, each governing the movement of a biomarker from one compartment into the next. Into these equations, one can plug known values &mdash; such as how fast a particular type of tumor grows, how much of the biomarker a tumor cell of this type sheds per hour and the minimum levels of the biomarker that must be present in the blood for a currently available assay to detect it.<br /><br />As a test case, Gambhir and Hori chose CA125, a well-studied biomarker shed into blood by ovarian tumors. Ovarian cancer is a notorious example of a condition for which early detection would make a huge difference in survival outcomes.<br /><br />CA125 is a protein made almost exclusively by ovarian tumor cells. The pharmacokinetics, metabolic fates, typical amounts secreted by an ovarian cell and other properties of CA125 are all well-known, as are ovarian tumors' typical growth rates, making it excellent for "road testing" with Gambhir and Hori's model. CA125 is by no means the ideal biomarker, said Gambhir, just one that can be used to help better understand ideal properties of biomarkers for early ovarian cancer detection.<br /><br />Applying their equations to CA125, Gambhir and Hori showed that before the currently best available test for CA125 could reliably detect an ovarian tumor, the tumor would need to reach a size of about 1.7 billion cells, or the volume of a cube with about a 2-cm edge. That would take about 10.1 to 12.6 years of development, at typical tumor-growth rates, from the first, single cancer cell.<br /><br />The model further calculated that a biomarker otherwise equivalent to CA125 but shed only by ovarian tumor cells would allow reliable detection within 7.7 years, when a tumor's size would be that of a tiny cube about one-sixth of an inch high.<br /><br />In the last decade, many potential new biomarkers for different cancers have been identified. There's no shortage of promising candidates &mdash; six for lung cancer alone, for example. But validating a biomarker in large clinical trials is a long, expensive process. So it is imperative to determine as efficiently as possible which, among many potential tumor biomarkers, is the best prospective candidate.<br /><br />"This model could take some of the guesswork out of it," Gambhir said. "It can be applied to all kinds of solid cancers and prospective biomarkers as long as we have enough data on, for instance, how much of it a tumor cell secretes per hour, how long the biomarker can circulate before it's degraded and how quickly tumor cells divide.<br /><br />"We can tweak one or another variable &mdash; for instance, whether a biomarker is also made in healthy tissues or just the tumor, or assume we could manage to boost the sensitivity of our blood tests by 10-fold or 100-fold &mdash; and see how much it advances our ability to detect the tumor earlier on."<br /><br />There are now new detection technologies capable of detecting biomarkers at concentrations as low as a few hundred molecules per mm (cc) of blood. A couple of years ago, Gambhir and his colleagues reported on one such developing technology: so-called magneto-nanosensors that can detect biomarkers with a 100-fold greater sensitivity than current methods.<br /><br />Better biomarker detection alone might shrink the time an ovarian tumor can grow before detection to about nine years, said Gambhir.<br /><br />A second priority is to come up with new and better biomarkers. "It's really important for us to find biomarkers that are made exclusively by tumor cells," he said.<br /><br />Under the right conditions (a highly sensitive assay measuring levels of a biomarker that is shed only by cancer cells), Gambhir said, the model predicts that a tiny tumor with a volume equivalent to a cube less than one-fifteenth of an inch on a side could be spotted.&nbsp;</p>]]></description>
        <guid>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3aa78fd67b-5105-421e-825a-e5aa172e1066&amp;sid=sitelife.wusa9.com</guid>
        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Tamoxifen's Effect on Male Breast Cancer Patients]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3ab1eb5903-4ebf-48ba-8c7a-9757c2008292&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Wed, 16 Nov 2011 00:31:00 GMT</pubDate>
        <description><![CDATA[<p>Male breast cancer patients stop taking tamoxifen early because of drug-related side effects<br /><br />The largest study to investigate the tolerability of the breast cancer drug tamoxifen in male breast cancer patients has shown that men stop taking their prescribed therapy early because of problems with side effects caused by the drug. <br /><br />The authors of the research paper, published today in the cancer journal Annals of Oncology [1], looked at records of 64 male breast cancer patients at their institution who had received tamoxifen for an average of four years and found that 53% (34) of the patients experienced one or more drug-related side effects. Of these 64 patients, 20.3% (13) of the men discontinued taking their prescribed tamoxifen therapy early because of the side effects. The research suggests that male breast cancer patients who discontinue tamoxifen therapy early may have an increased risk of the cancer recurring. <br /><br />Male breast cancer is a rare disease and the world age-standardised incidence rate is 0.4 per 100,000 in men compared with 66.7 per 100,000 in women [2]. Tamoxifen is the standard of care for the hormone treatment of men with breast cancer and works by blocking the growth-promoting action of the hormone oestrogen on the cancer cells. Almost all (90%) breast cancers in men are hormone-receptor-positive and drugs that target the hormone oestrogen are usually given after surgery. <br /><br />Dr Naveen Pemmaraju, who carried out the research under the direction of Dr Sharon Giordano at the Department of Breast Medical Oncology at the University of Texas MD Anderson Cancer Center, Houston, USA, said "This is the largest study to specifically assess tamoxifen-related side effects in men because in our institution we treated a relatively large number of male breast cancer patients. We found that, after adjusting for patient age and stage of the disease, the prognosis for men with breast cancer is similar to that of women. Tamoxifen has been shown to improve survival rates for breast cancer patients, so early discontinuations may have the potential to increase the risk of the cancer recurring in this group of male breast cancer patients.<br /><br />"Male breast cancer is a very rare and unique cancer affecting approximately 2,000 men in the USA per year. As there are so few male breast cancer cases, clinical practice and optimal treatment strategies have been extrapolated from female breast cancer patients with very little published evidence to guide clinical decisions. In our institution, we noted that several of our male patients were having difficulty with taking tamoxifen therapy, and these side effects appeared to be a little bit different to those reported with women receiving the same drug."<br /><br />Weight gain and loss of sex drive were the most frequently occurring tamoxifen-related side effects observed in the study. Of the 13 male patients who stopped taking tamoxifen early because of side effects, four of the discontinuation decisions (31%) were physician-directed (four thromboembolic events) and nine (69%) were patient-directed preferences based on the intolerable side-effects. Nine patients died after stopping tamoxifen early in the study. <br /><br /> Dr Pemmaraju said: "Tamoxifen is a hormonal treatment, specifically an anti-oestrogen. We think that men might experience some different side effects than women because men have a different hormonal environment than women (for instance they have more testosterone and less oestrogen). This difference in hormone levels could result in different side effects when using a drug that blocks hormones.<br /><br />"The results of this study should not change the recommendation for prescribing tamoxifen for male breast cancer patients. However, clinicians need to be aware of the possible side effects that men may experience when receiving tamoxifen so that the patients can be counselled appropriately," Dr Pemmaraju added. "This study also highlights the importance of funding and conducting research for rare disease so that we understand the true toxicities and benefits of treatment.<br /><br />"Our next step will be to prospectively collect data on the side effects that men get when they are prescribed to take tamoxifen for breast cancer. This follow-up study will be very important because it will provide much more detailed and comprehensive information on the tolerability profile of tamoxifen in male breast cancer patients," Dr Pemmaraju concluded.<br /><br />Male breast cancer is very rare and statistical records are not available for most European countries. In the UK, around 300 men are diagnosed with breast cancer each year compared with about 45,700 cases in women. In the US in 2011, about 2,140 new cases of invasive breast cancer will be diagnosed in men compared with 230,480 new cases in women and approximately 450 men will die from breast cancer compared with 39,520 women.<br /><br />###&nbsp;</p>]]></description>
        <guid>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3ab1eb5903-4ebf-48ba-8c7a-9757c2008292&amp;sid=sitelife.wusa9.com</guid>
        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Thoughts &amp; Feelings After Breast Cancer]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3acaa3be9b-e96e-4fa2-b9a3-09ceb720a213&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Tue, 15 Nov 2011 13:28:00 GMT</pubDate>
        <description><![CDATA[<p>Neurological and executive function impairment associated with breast cancer<br /><br />CHICAGO &ndash; Women who survive breast cancer show significant neurological impairment, and outcomes appear to be significantly poorer for those treated with chemotherapy, according to a report in the November issue of the Archives of Neurology, one of the JAMA/Archives journals.<br /><br />Breast cancer (BC) is one of the most common public health problems, with a worldwide estimated incidence of 39 per 100,000 individuals annually. Although primary BC has not been associated historically with neurological problems, a growing body of evidence suggests that patients are at increased risk for altered brain structure and function, according to background information in the article.<br /><br />Shelli R. Kesler, Ph.D., and colleagues at Stanford University School of Medicine, Stanford, Calif., conducted an observational study to determine whether profiles of brain activation differ among BC survivors treated with or without chemotherapy, compared with healthy control women. The study included 25 women with BC who received chemotherapy, 19 women with BC who did not receive chemotherapy, and 18 healthy female controls, all matched for age and other demographic variables. The women were asked to perform various tasks, and the researchers used functional MRI to measure activation in several areas of the brain.<br /><br />"Women with BC demonstrated significantly reduced activation in the left middle dorsolateral prefrontal cortex and premotor cortex compared with healthy controls," the authors report.<br /><br />"The chemotherapy group also demonstrated significantly reduced left caudal lateral prefrontal cortex activation and increased perseverative errors and reduced processing speed compared with the other two groups," they write.<br /><br />The study also found that the negative effects of chemotherapy on brain function may be exacerbated by such factors as increased age and lower educational level.<br /><br />"This study provides further evidence that primary BC may cause measurable brain injury," the authors conclude. "Women treated with chemotherapy may show additional prefrontal deficits and have difficulty compensating for neurobiological changes such that they also show impaired executive function."&nbsp;</p>]]></description>
        <guid>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3acaa3be9b-e96e-4fa2-b9a3-09ceb720a213&amp;sid=sitelife.wusa9.com</guid>
        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Computers Playing A Role In Breast Cancer Detection]]></title>
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        <pubDate>Thu, 10 Nov 2011 12:29:00 GMT</pubDate>
        <description><![CDATA[<p>Stanford team trains computer to evaluate breast cancer<br />STANFORD, Calif. &mdash; Since 1928, the way breast cancer characteristics are evaluated and categorized has remained largely unchanged. It is done by hand, under a microscope. Pathologists examine the tumors visually and score them according to a scale first developed eight decades ago. These scores help doctors assess the type and severity of the cancer and, accordingly, to calculate the patient's prognosis and course of treatment.<br /><br />In a paper to be published Nov. 9 in Science Translational Medicine, computer scientists at the Stanford School of Engineering and pathologists at the Stanford School of Medicine report their collaboration to train computers to analyze breast cancer microscopic images. The computer analyses were more accurate than those conducted by humans.<br /><br />Their model is called Computational Pathologist, or C-Path, a machine-learning-based method for automatically analyzing images of cancerous tissues and predicting patient survival.<br /><br />To train C-Path, the researchers used existing tissue samples taken from patients whose prognosis was known. The computers pored over images, measuring various tumor structures and trying to use those structures to predict patient survival. By comparing results against the known data, the computers adapted their models to better predict survival and gradually figured out what features of the cancers matter most and which matter less in predicting survival.<br /><br />"In essence, the computer learns," said Daphne Koller, PhD, professor of computer science and senior author of the paper.<br /><br />Medical science has long used three specific features for evaluating breast cancer cells &mdash; what percentage of the tumor is comprised of tube-like cells, the diversity of the nuclei in the outermost (epithelial) cells of the tumor and the frequency with which those cells divide (a process known as mitosis). These three factors are judged by sight with a microscope and scored qualitatively to stratify breast cancer patients into three groups that predict survival rates.<br /><br />"Pathologists have been trained to look at and evaluate specific cellular structures of known clinical importance, which get incorporated into the grade. However, tumors contain innumerable additional features, whose clinical significance has not previously been evaluated," said Andrew Beck, MD, a doctoral candidate in biomedical informatics and the paper's first author.<br /><br />"The computer strips away that bias and looks at thousands of factors to determine which matter most in predicting survival," said Koller.<br /><br />C-Path, in fact, assesses 6,642 cellular factors. Once trained using one group of patients, C-Path was asked to evaluate tissues of cancer patients it had not checked before and the result was compared against known data. Ultimately, C-Path yielded results that were a statistically significant improvement over human-based evaluation.<br /><br />What's more, the computers identified structural features in cancers that matter as much or more than those that pathologists have focused on traditionally. In fact, they discovered that the characteristics of the cancer cells and the surrounding cells, known as the stroma, were both important in predicting patient survival.<br /><br />"We built a model based on features of the stroma &mdash; the microenvironment between cancer cells &mdash; that was a stronger predictor of outcome than one built exclusively from features of epithelial cells," said Beck. "The stromal model was as predictive as the model built from both stromal and epithelial features."<br /><br />In the end, the Stanford findings add weight to what many scientists have been contending for some time: that cancer is an "ecosystem," and that clinically significant information can be obtained by careful analysis of the complete tumor microenvironment.<br /><br />"Through machine learning, we are coming to think of cancer more holistically, as a complex system rather than as a bunch of bad cells in a tumor," said Matt van de Rijn, MD, PhD, a professor of pathology and co-author of the study. "The computers are pointing us to what is significant, not the other way around."<br /><br />Van de Rijn does not see computers replacing pathologists. "We're looking at a future where computers and humans collaborate to improve results for patients across the world," he said.<br /><br />The impact of the Stanford work will be felt broadly and individually, the researchers said. In the widest sense, having computers that can evaluate cancers will bring world-class pathology to underserved areas where trained professionals have traditionally been scarce, improving the prognosis and treatment of breast cancer for millions in developing areas of the world.<br /><br />At the personal level, machine learning may reduce the variability in results. C-Path could improve the accuracy of prognoses for all breast cancer victims. It could, likewise, improve the screening of pre-cancerous cells that could help many women avoid cancer altogether. It might even be applied to predict the effectiveness of various forms of treatment and drug therapies.<br /><br />"If we can teach computers to look at a tumor tissue sample and predict survival, why not train them to predict from the same sample which courses of treatment or drugs a given patient might respond to best? Or even to look at samples of non-malignant cells to predict whether these benign tissues will turn cancerous," said Koller. "This is personalized medicine."<br /><br /><br />&nbsp;</p>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[Bosses, Get With It When A Breast Cancer Survivor Returns To Work]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3ad1775ae6-af02-49e2-914a-13659dabbf4e&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Tue, 08 Nov 2011 13:09:00 GMT</pubDate>
        <description><![CDATA[<h2 class="subtitle">Review covered the employment experiences of nearly 1,200 women from five countries</h2><p>Employers need to be more aware of the capabilities of women affected by breast cancer and provide them with better support, backed by employment directives and occupational health policies, according to a paper in the November issue of the <i>European Journal of Cancer Care</i>.</p><p>A review carried out by Dr Maggi Banning, from Brunel University, Uxbridge, UK, also showed that healthcare professionals need to provide breast cancer patients and survivors with better information about the best time to return to work.</p><p>Dr Banning reviewed ten studies on the employment experiences of 1,181 women affected by the disease from the USA, Canada, UK, Sweden and Denmark published between 1991 and 2010.</p><p>"Employment is an important factor in the lives of people with cancer as a return to work is often associated with a return to normality" says Dr Banning, a senior lecturer in clinical practice at the University.</p><p>"But it is clear that there are considerable differences in women's experiences of returning to work. Some positive working practices were reported, but other organisations were guilty of a culture of ignorance. Many of the negative experiences centred on the unrealistic expectations and inflexibility of some employers, lack of support from colleagues and mistaken assumptions about the woman's physical appearance."</p><p><b>Key findings of the study included:</b></p><p>Some women felt that returning to work was a welcome distraction from life as a cancer patient and provided a sense of normality, structure to their day, belonging, identity and social connections. However, others were apprehensive because of low perceptions of their physical fitness and work capacity after treatment and concerns about what their employer would expect of them.</p><p>Financial pressures were a common driver, with studies estimating that half the women could no longer afford to remain off work. Some women even missed scheduled treatment sessions as it would have meant taking time off work. Lack of sick pay and concerns about losing their job were also common.</p><p>While many women felt positive about returning to work, some reported that they had re-evaluated their lives after their diagnosis and felt that work no longer held the same importance it used to. The work aspirations of some women were also reduced.</p><p>Coping with cancer or the side effects of treatment, such as fatigue and sickness, often had an impact on the women's health. Loss of confidence and emotional issues also proved problematic for some women.</p><p>Women reported that employers' expectations of their work capacity varied, and while some studies found examples of supportive employers and colleagues, this was not always the case. Women in Europe appeared to have a more supportive work environment than those in the USA and Canada.</p><p>Some women took up different positions or were able to reduce their working hours so that they could receive treatment and recover from the side effects. However, in some cases, work modifications were refused and employers were openly hostile, insisting that they should resign from their jobs or retire.</p><p>A number of employers judged women by their physical appearance, not realising that up to a quarter of women experience residual fatigue for many months after treatment. Colleagues were also misled by women's physical appearance and this could to lead to lack of sympathy and work-related support.</p><p><b>Dr Banning has come up with a number of recommendations as a result of her review:</b></p><p>Employers need to be better educated to avoid the culture of ignorance that exists within some organisations when it comes to the capabilities of women affected by breast cancer.</p><p>There is room for improvement in the way that healthcare professionals and employers manage the return to work process.</p><p>Occupational health departments need to ensure that all cancer survivors have a fitness to work assessment before returning and need to provide managers with realistic guidelines of what they can expect from their employee.</p><p>Directives are also needed to influence and change welfare and employment policies to better support and manage the return to work process, including time off to attend treatments and follow-up appointments.</p><div align="center">###</div>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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        <title><![CDATA[A Knowledge Gap in Canada When It Comes To Breast Reconstruction After A Mastectomy]]></title>
                <link>http://www.wusa9.com/life/community/persona.aspx?U=8977f724bb534293b2789bfc37d6e6cf&amp;plckController=PersonaBlog&amp;plckScript=personaScript&amp;plckElementId=personaDest&amp;plckPersonaPage=BlogViewPost&amp;plckPostId=Blog%3a8977f724bb534293b2789bfc37d6e6cfPost%3a54995647-a63a-4734-a199-8359694f0cdd&amp;sid=sitelife.wusa9.com</link>
        <pubDate>Tue, 08 Nov 2011 13:07:00 GMT</pubDate>
        <description><![CDATA[<h1 class="title">Rates of breast reconstruction after mastectomy in Canada</h1><h2 class="subtitle">&nbsp;</h2><p>Few patients in Canada undergo breast reconstruction after mastectomy, despite its safety as a procedure and the positive psychological benefits, states a review article in <i>CMAJ</i> (<i>Canadian Medical Association Journal</i>).</p><p>The article reviews rates of breast reconstruction and factors that influence the practice of immediate reconstruction in patients with early stage breast cancer. However, information is lacking on the current rate and factors that influence this procedure in Canada.</p><p>Rates in Canada have been historically low, with a reconstruction rate of 7.7% in Ontario (1994/95) and 3.8% in Nova Scotia from 1991. In contrast, rates were higher in Australia (9.9%, 1982), Denmark (14%, 1999) and England (16.5%, 2006). In the United States, rates for breast reconstruction have increased from as low as 3.4% in 1985 to a high of 42% from 1997 in a network of tertiary cancer centres. Use of immediate reconstruction at the same time as mastectomy has also increased in the US, in part due to a recommendation by the Commission on Cancer of the American College of Surgeons in 2001 to incorporate this practice in the treatment of early stage breast cancer.</p><p>In general, older age, ethnicity, socioeconomic status and geography affect the use of breast reconstruction. Women older than 50 years are less likely to undergo reconstruction. This may be secondary to concerns of increased complications or comorbidities, although a US study found that the negative relationship between advanced age and decreased breast reconstruction remained significant after controlling for patient comorbidities. Women of lower socioeconomic status were less likely to have reconstruction. Women living in large urban centres were more likely to undergo breast reconstruction. For example, there were 10 reconstructions per 100 mastectomies in the Toronto area compared with 4.3 per 100 mastectomies in the rest of Ontario in 1994/1995. Other modifiable barriers to breast reconstruction in Canada include knowledge gaps and misperceptions held by referring physicians.</p><p>The stage of breast cancer is the most predictive clinical factor associated with reconstruction, because patients with advanced stage disease are significantly less likely to undergo reconstructive surgery than those with early stage disease.</p><p>"Although higher stage disease is not a contraindication for breast reconstruction, women or their physicians, or both, may not perceive this restorative procedure as a high priority compared with treatment," writes Dr. Toni Zhong, Department of Surgery and Surgical Oncology, University Health Network, University of Toronto, with coauthors.</p><p>"The optimal rate of breast reconstruction is not currently known for any jurisdiction, and the absence of such a benchmark limits useful research in this area," write the authors. "However, given the broad array of factors that influence the rate of breast reconstruction and the low rate of breast reconstruction in Canada compared with other jurisdictions, it is unlikely that our current practice has achieved an optimal rate."</p><p>The authors suggest that having a better understanding of the current rates of breast reconstruction and the different factors that influence access to breast reconstruction in Canada is key to addressing our current knowledge gap.</p>]]></description>
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        <dc:creator><![CDATA[AndreaRoane]]></dc:creator>
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