{"id":279,"date":"2014-06-26T08:57:11","date_gmt":"2014-06-26T12:57:11","guid":{"rendered":"http:\/\/blogs.shu.edu\/cancer\/?p=279"},"modified":"2021-07-02T08:52:00","modified_gmt":"2021-07-02T12:52:00","slug":"parp-inhibitor-rejected-by-fda-advisory-committee","status":"publish","type":"post","link":"https:\/\/blogs.shu.edu\/cancer\/2014\/06\/26\/parp-inhibitor-rejected-by-fda-advisory-committee\/","title":{"rendered":"PARP inhibitor rejected by FDA Advisory Committee, then Approved for refractory patients"},"content":{"rendered":"

In June 2014, the FDA Oncology Drug Advisory Committee voted 11-2 to delay approval of AstraZeneca\u2019s olaparib, a PARP (poly-ADP ribose polymerase) inhibitor for maintenance therapy in patients with ovarian cancer.\u00a0 The product received Accelerate Approval designation from the FDA, which provides for conditional approval pending follow-up studies, based on surrogate endpoints from Phase 2 trials, in this case, progression-free survival (PFS).\u00a0 The advisory panel wants to wait to see the results of a larger Phase 3 study that is ongoing in patients with BRCA1 and BRCA2 mutations, which is evaluating the outcome of overall survival (OS). However, in December, the FDA approved the product for a different claim –\u00a0\u00a0patients with gBRCAm-associated ovarian cancer<\/a> who have received three or more chemotherapy treatments<\/p>\n

I believe that the drug should have been approved in June, under the Accelerated Approval program.\u00a0 In the subset of patients with BRCA mutations enrolled in the Phase 2 study, there was an 83% reduction in the risk of progression.\u00a0 This is amazing, especially in ovarian cancer where patients relapse frequently following courses of treatment.\u00a0 So, extending the time between relapse means that the patients will have to undergo fewer courses of very toxic chemotherapy.<\/p>\n

PARP (poly-ADP ribose polymerase) repairs single strand DNA breaks before double strand breaks can develop.\u00a0 Double strand breaks are toxic to cells \u2013 they trigger p53-mediated apoptosis, or can lead to crisis and p53-independent apoptosis if the repairs cannot be fixed.\u00a0 BRCA1 and BRCA2 repair double strand breaks, so, in patients with mutations to BRCA, the inability to repair dsDNA breaks results in cell death. [Diagram – see Update on PARP inhibitors in clinical trials ie iniparib, olaparib, veliparib, PF-01367338, CEP-9722. Veliparib is being tested in ISPY2 in neoadjuvant breast cancer.]<\/p>\n

\"PARP\"<\/a><\/p>\n

This drug could have certainly been labeled to address the downsides raised by the panel, including the risk of second malignancies, which were seen in 2.2% of the patients receiving treatment with olaparib.\u00a0 The panel felt that this is a higher incidence than would be expected.\u00a0 [Seeing melodysplastic syndrome and acute myelogenous leukemia in patients in the study makes sense, given the prior platinum-based treatments that the patients received AND the mechanism of action of olaparib, which will lead to single-strand breaks in DNA, which are mutagenic.]<\/p>\n

I feel that the labeling of the product can address the safety concerns for maintenance therapy such that the benefits to patients can outweigh the risks. I am thrilled that it was approved, at least for the refractory claim.<\/p>\n

Here\u2019s the link\u2026tell me what you think<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

In June 2014, the FDA Oncology Drug Advisory Committee voted 11-2 to delay approval of AstraZeneca\u2019s olaparib, a PARP (poly-ADP ribose polymerase) inhibitor for maintenance therapy in patients with ovarian cancer.\u00a0 The product received Accelerate Approval designation from the FDA, which provides for conditional approval pending follow-up studies, based on surrogate endpoints from Phase 2 […]<\/p>\n","protected":false},"author":2252,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"categories":[26,24,31],"tags":[155,148,149,1129,156,152,157,154,147,151,150,153],"class_list":["post-279","post","type-post","status-publish","format-standard","hentry","category-dna-repair","category-mutations","category-traditional-chemotherapy","tag-accelerated-approval","tag-brca1","tag-brca2","tag-fda","tag-oncology-drug-advisory-committee","tag-os","tag-ovarian-cancer","tag-overall-survival","tag-parp","tag-pfs","tag-platinum","tag-progression-free-survival"],"post_mailing_queue_ids":[],"_links":{"self":[{"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/posts\/279","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/users\/2252"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/comments?post=279"}],"version-history":[{"count":4,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/posts\/279\/revisions"}],"predecessor-version":[{"id":5017,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/posts\/279\/revisions\/5017"}],"wp:attachment":[{"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/media?parent=279"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/categories?post=279"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.shu.edu\/cancer\/wp-json\/wp\/v2\/tags?post=279"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}