{"id":184046,"date":"2015-02-16T17:44:59","date_gmt":"2015-02-16T22:44:59","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/cancer-gene-therapy-advances.php"},"modified":"2015-02-16T17:44:59","modified_gmt":"2015-02-16T22:44:59","slug":"cancer-gene-therapy-advances","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/cancer-gene-therapy-advances.php","title":{"rendered":"Cancer gene therapy advances"},"content":{"rendered":"<p><p>  Flow chart of one method of engineering T cells to fight cancer.<\/p>\n<p>    Tough blood cancers are responding    to     treatment with the patient's own genetically engineered    immune cells, according to a cancer specialist who is helping    test the bold -- and risky -- approach.  <\/p>\n<p>    The treatment has produced    complete remissions in large percentages of patients treated,    up to 90 percent in one group of 30 patients. Moreover, these    are all extremely sick patients, whose cancer has resisted    other therapies, leaving them with virtually no options. The    longest survivor has been in complete remission for more than 4    years, said Dr. David Porter of the University of    Pennsylvania.  <\/p>\n<p>    Porter spoke Sunday at the        35th Annual Conference on Clinical Hematology &    Oncology, held in La Jolla by Scripps Health. Speakers like    Porter came from around the country to discuss advances in    their field, part of a continuing medical education program to    keep doctors up to date with the latest medical advances. The    conference continues through Tuesday.  <\/p>\n<p>          Dr. David Porter \/ University of Pennsylvania        <\/p>\n<p>    Porter works with     Dr. Carl June and other colleagues to hone the    effectiveness of using T cells genetically programmed to attack    malignant B cells. B cell malignancies cause such cancers as    chronic lymphocytic leukemia, or CLL; acute lymphoblastic    leukemia, or ALL, and non-Hodgkin's lymphoma.  <\/p>\n<p>    The genetically altered T cells are given an artificially    created gene to produce a     chimeric antigen receptor. This receptor recognizes the    protein CD19, produced almost exclusively on B cells. The T    cells hone in on this protein and kill the B cells. When the    cancer is knocked down, some of the T cells remain behind,    ready to pounce on any recurrence.  <\/p>\n<p>    The trials are now expanding to include myloma, Porter said.    For more information on the university's T cell-based clinical    trials, go to <a href=\"http:\/\/www.penncancer.org\/tcelltherapy\" rel=\"nofollow\">http:\/\/www.penncancer.org\/tcelltherapy<\/a>.  <\/p>\n<p>    June's team began testing the therapy in 2010 in CLL patients    and then in those with ALL. These were all patients with    relapsed cancers that had become resistant to other therapies.    The therapy has been progressively refined, Porter said. Other    centers have developed their own versions of this therapy.  <\/p>\n<p>    In October, 2014, the University of Pennsylvania and Children's    Hospital of Philadelphia announced that 27 out of 30 patients    with relapsed ALL achieved a complete remission within one    month of treatment, and 23 were still alive 6 months after    treatment. As of October, 19 of the patients remained in    remission. Most treated, 25 out of 30, were children. The    response rate with CLL is about 47 percent, Porter said.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read more:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.utsandiego.com\/news\/2015\/feb\/15\/cancer-car-cells-scripps-porter\" title=\"Cancer gene therapy advances\">Cancer gene therapy advances<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Flow chart of one method of engineering T cells to fight cancer. Tough blood cancers are responding to treatment with the patient's own genetically engineered immune cells, according to a cancer specialist who is helping test the bold -- and risky -- approach. The treatment has produced complete remissions in large percentages of patients treated, up to 90 percent in one group of 30 patients <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/gene-therapy\/cancer-gene-therapy-advances.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":[24],"tags":[],"class_list":["post-184046","post","type-post","status-publish","format-standard","hentry","category-gene-therapy"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/184046"}],"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=184046"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/184046\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=184046"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=184046"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=184046"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}