{"id":39792,"date":"2014-09-30T01:42:20","date_gmt":"2014-09-30T05:42:20","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/crizotinib-treatment-effective-against-ros1-positive-lung-cancer-study-suggests\/"},"modified":"2014-09-30T01:42:20","modified_gmt":"2014-09-30T05:42:20","slug":"crizotinib-treatment-effective-against-ros1-positive-lung-cancer-study-suggests","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/crizotinib-treatment-effective-against-ros1-positive-lung-cancer-study-suggests\/","title":{"rendered":"Crizotinib treatment effective against ROS1-positive lung cancer, study suggests"},"content":{"rendered":"<p><p>  Treatment with the targeted therapy drug crizotinib effectively  halts the growth of lung tumors driven by rearrangements of the  ROS1 gene. In an article receiving Online First publication in  the New England Journal of Medicine to coincide with a  presentation at the European Society for Medical Oncology  meeting, an international research team reports that crizotinib  treatment led to significant tumor shrinkage in 36 of 50 study  participants and suppressed tumor growth in another 9.<\/p>\n<p>    \"Prior to this study, there were a handful of reports    describing marked responses to crizotinib in individual    patients with ROS1-positive lung tumors,\" says Alice Shaw, MD,    PhD, of the Massachusetts General Hospital (MGH) Cancer Center,    lead author of the NEJM report. \"This is the first definitive    study to establish crizotinib's activity in a large group of    patients with ROS1-positive lung cancer and to confirm that    ROS1 is a bona fide therapeutic target in those patients.\"  <\/p>\n<p>    Crizotinib currently is FDA-approved to treat non-small-cell    lung cancers (NSCLC) driven by rearrangments in the ALK gene,    which make up around 4 percent of cases. An MGH Cancer Center    report published in 2012 reported that 1 to 2 percent of NSCLCs    are driven by rearrangements in ROS1, which encodes a protein    with significant structural similarities to that encoded by the    ALK gene.  <\/p>\n<p>    The current study, an expansion of the original phase 1    crizotinib trial, enrolled 50 patients with ROS1-positive    NSCLC, beginning in late 2010. Patients received twice daily    doses of crizotinib. As noted above, tumor size was    significantly reduced in 72 percent of patients and tumor    growth was halted in an additional 18 percent. The average    duration of response was over 17 months. At the end of the    study, 25 of the 50 patients were still receiving crizotinib    with no evidence of tumor progression.  <\/p>\n<p>    As with other targeted cancer therapy drugs, treatment    resistance developed in a number of participants, but the    effectiveness of crizotinib appeared to last longer in    ROS1-positive patients than in patients with ALK-positive    tumors. \"Almost all patients treated with targeted therapies    eventually develop resistance,\" explains Shaw, an associate    professor of Medicine at Harvard Medical School (HMS).    \"Fortunately, the remissions induced by crizotinib in    ROS1-positive patients are quite prolonged, and resistance    appears to emerge much later, on average, than what we have    seen with other targeted therapies for lung cancer and    melanoma.\"  <\/p>\n<p>    The authors note that development of efficient laboratory    diagnostics has been critical to identification of ROS1    rearrangements and of other genetic alterations that drive    tumor growth. John Iafrate, MD, PhD, medical director of the    MGH Center for Integrated Diagnostics and associate professor    of Pathology at HMS, who is senior author of the study    comments, \"This is a great example of success in personalized    medicine. While NSCLC patients with ROS1 fusions are rare, if    you devote the diagnostic laboratory resources to find that 1    to 2 percent of patients, you will make a real difference.\"  <\/p>\n<p>    While crizotinib's FDA approval currently covers only    ALK-positive NSCLC, Shaw notes that National Comprehensive    Cancer Network guidelines recommend that patients with advanced    lung cancer be considered for ROS1 testing and that crizotinib    should be used to treat ROS1-positive patients.  <\/p>\n<p>    Story Source:  <\/p>\n<p>    The above story is based on materials provided by    Massachusetts General    Hospital. Note: Materials may be edited for    content and length.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>View original post here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/www.sciencedaily.com\/releases\/2014\/09\/140927145928.htm\/RK=0\/RS=NHKa7q_0XkOBHGpCeU1b9DAwDnk-\" title=\"Crizotinib treatment effective against ROS1-positive lung cancer, study suggests\">Crizotinib treatment effective against ROS1-positive lung cancer, study suggests<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Treatment with the targeted therapy drug crizotinib effectively halts the growth of lung tumors driven by rearrangements of the ROS1 gene. In an article receiving Online First publication in the New England Journal of Medicine to coincide with a presentation at the European Society for Medical Oncology meeting, an international research team reports that crizotinib treatment led to significant tumor shrinkage in 36 of 50 study participants and suppressed tumor growth in another 9.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/crizotinib-treatment-effective-against-ros1-positive-lung-cancer-study-suggests\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[],"class_list":["post-39792","post","type-post","status-publish","format-standard","hentry","category-gene-medicine"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/39792"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=39792"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/39792\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=39792"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=39792"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=39792"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}