{"id":216628,"date":"2017-06-06T16:47:48","date_gmt":"2017-06-06T20:47:48","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/new-cancer-medicine-targets-rare-genetic-flaw-press-tv.php"},"modified":"2017-06-06T16:47:48","modified_gmt":"2017-06-06T20:47:48","slug":"new-cancer-medicine-targets-rare-genetic-flaw-press-tv","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/new-cancer-medicine-targets-rare-genetic-flaw-press-tv.php","title":{"rendered":"New cancer medicine targets rare genetic flaw &#8211; Press TV"},"content":{"rendered":"<p><p>  This file photo shows doctors at Memorial Sloan Kettering Cancer  Center in New York City.<\/p>\n<p>    An experimental cancer medicine called larotrectinib    has shown promise treating a diverse range of cancers in people    young and old, researchers said at a major cancer conference in    the United States.  <\/p>\n<p>    The treatment targets a genetic abnormality which is often    found in rare cancers - including salivary gland cancer,    juvenile breast cancer, and a soft tissue cancer known as    infantile fibrosarcoma - which are particularly difficult to    treat.  <\/p>\n<p>    This abnormality also occurs in about 0.5 percent to one    percent of many common cancers.  <\/p>\n<p>    In the study released at the American Society of Clinical    Oncology conference, 76 percent of cancer patients - both    children and adults with 17 different kinds of cancer -    responded well to the medicine.  <\/p>\n<p>    A total of 79 percent were alive after one year. The study is    ongoing.  <\/p>\n<p>    Twelve percent went into complete remission from their cancer.  <\/p>\n<p>    The clinical trial included 55 patients - 43 adults and 12    children. All had advanced cancers in various organs, including    the colon, pancreas and lung, as well as melanoma.  <\/p>\n<p>    \"These findings embody the original promise of precision    oncology: treating a patient based on the type of mutation,    regardless of where the cancer originated,\" said lead study    author David Hyman, chief of early drug development at Memorial    Sloan Kettering Cancer Center in New York.  <\/p>\n<p>    \"We believe that the dramatic response of tumors with TRK    fusions to larotrectinib supports widespread genetic testing in    patients with advanced cancer to see if they have this    abnormality.\"  <\/p>\n<p>    Made by Loxo Oncology Inc., larotrectinib is a selective    inhibitor of tropomyosin receptor kinase (TRK) fusion proteins.  <\/p>\n<p>    TRK proteins are a product of a genetic abnormality when a TRK    gene in a cancer cell fuses with one of many other genes,    researchers said.  <\/p>\n<p>    The US Food and Drug Administration has not yet approved the    treatment for widespread use.  <\/p>\n<p>    The treatment was well tolerated by patients, and the most    common side effects were fatigue and mild dizziness.  <\/p>\n<p>    \"If approved, larotrectinib could become the first therapy of    any kind to be developed and approved simultaneously in adults    and children, and the first targeted therapy to be indicated    for a molecular definition of cancer that spans all    traditionally-defined types of tumors,\" said Hyman.  <\/p>\n<p>    (Source:AFP)  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Original post:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/presstv.ir\/Detail\/2017\/06\/04\/524199\/US-cancer-treatment-medicine-patients-research\" title=\"New cancer medicine targets rare genetic flaw - Press TV\">New cancer medicine targets rare genetic flaw - Press TV<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> This file photo shows doctors at Memorial Sloan Kettering Cancer Center in New York City. An experimental cancer medicine called larotrectinib has shown promise treating a diverse range of cancers in people young and old, researchers said at a major cancer conference in the United States.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/new-cancer-medicine-targets-rare-genetic-flaw-press-tv.php\">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":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[5],"tags":[],"class_list":["post-216628","post","type-post","status-publish","format-standard","hentry","category-genetic-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/216628"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=216628"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/216628\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=216628"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=216628"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=216628"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}