{"id":1276,"date":"2020-08-21T07:01:00","date_gmt":"2020-08-21T07:01:00","guid":{"rendered":"https:\/\/aceoncology.org\/insights-on-treatment-sequencing-in-advanced-braf-mutant-melanoma"},"modified":"2021-03-05T05:10:23","modified_gmt":"2021-03-05T05:10:23","slug":"insights-on-treatment-sequencing-in-advanced-braf-mutant-melanoma","status":"publish","type":"post","link":"https:\/\/aceoncology.org\/zh-hans\/insights-on-treatment-sequencing-in-advanced-braf-mutant-melanoma\/","title":{"rendered":"Insights on Treatment Sequencing in Advanced BRAF-mutant Melanoma"},"content":{"rendered":"\n<p>The treatment landscape for patients with advanced (unresectable or metastatic) melanoma has changed dramatically over the last 5-10 years with the availability of targeted therapies and immune checkpoint inhibitors (ICIs). Around half of all melanomas harbor mutations in the <em>BRAF <\/em>gene, with V600E\/K being the most common mutation. The standard of care for patients with <em>BRAF <\/em>mutation-positive advanced melanoma has shifted from single-agent BRAF inhibition to combination therapy with BRAF and MEK inhibitors (BRAFi; MEKi) as well as immunotherapy. However, the optimal sequencing of targeted and immunotherapy regimens for maximum efficacy and tolerability in patients with <em>BRAF <\/em>V600E\/K mutation-positive advanced melanoma is still a matter of debate.<\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p>A recent publication describes a <a href=\"https:\/\/jamanetwork.com\/journals\/jamaoncology\/article-abstract\/2768018\" rel=\"noreferrer noopener\" target=\"_blank\">post-hoc subgroup analysis<\/a>of pooled data from 3 multinational, multicenter studies: <a href=\"https:\/\/www.annalsofoncology.org\/article\/S0923-7534(19)31110-X\/fulltext\" rel=\"noreferrer noopener\" target=\"_blank\">KEYNOTE-001<\/a>, <a href=\"https:\/\/www.thelancet.com\/journals\/lanonc\/article\/PIIS1470-2045(15)00083-2\/fulltext\" rel=\"noreferrer noopener\" target=\"_blank\">KEYNOTE-002<\/a> and <a href=\"https:\/\/www.thelancet.com\/journals\/lanonc\/article\/PIIS1470-2045(19)30388-2\/fulltext\" rel=\"noreferrer noopener\" target=\"_blank\">KEYNOTE-006<\/a>, with the objective of assessing whether <em>BRAF <\/em>V600E\/K mutation status or previous BRAFi therapy with or without MEKi affected patients\u2019 response to the PD-1 inhibitor, pembrolizumab. The analysis included data from 1,558 patients with advanced melanoma and known <em>BRAF <\/em>mutation status, who had all received pembrolizumab, and some who had also received BRAFi with or without MEKi. The primary endpoints, which were objective response rate (ORR), 4-year progression free survival (PFS) rate and 4-year overall survival (OS) rate, were compared between subgroups. For patients with <em>BRAF <\/em>wild type (wt) melanoma, the ORR was 39.8% versus 34.3% for <em>BRAF <\/em>mutant melanoma, the 4-year PFS rate was 22.9% and 19.8%, respectively, and the 4-year OS rate was 37.5% and 35.1%. In patients who had, or had not, received prior BRAFi, with or without MEKi therapy, ORR was 28.4% versus 44.2%, 4-year PFS rate was 15.2% versus 27.8%, and 4-year OS rate was 26.9% versus 49.3%, respectively. One theory for the lower response and survival rates in patients who had been previously treated with BRAFi with\/without MEKi, was the imbalance in baseline characteristics between the two groups. A higher number of patients who had previously received targeted therapy had baseline characteristics that indicated a worse prognosis, such as PD-L1 negative tumors, elevated lactate dehydrogenase (LDH) levels, higher Eastern Cooperative Oncology Group (ECOG) performance status, larger baseline tumors and lower albumin levels. There was no meaningful difference in the safety profile among patients treated with pembrolizumab in the four subgroups.<\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p>Overall, the results of this post hoc pooled subgroup analysis indicate that the PD-1 inhibitor may provide clinical benefit in patients who are <em>BRAF <\/em>wt or <em>BRAF <\/em>mutant, and in patients whowere, or were not, previously treated with targeted therapy, and support its use in the treatment of patients regardless of <em>BRAF <\/em>mutation status or previous therapy. Ongoing randomized clinical trials of immunotherapy and targeted therapy for patients with <em>BRAF <\/em>V600E\/K-mutated advanced melanoma may further clarify optimal sequencing. Indeed, in the phase III <a href=\"https:\/\/www.thelancet.com\/journals\/lancet\/article\/PIIS0140-6736(20)30934-X\/fulltext?hss_channel=tw-27013292\" rel=\"noreferrer noopener\" target=\"_blank\">IMspire trial<\/a> that compared the PD-L1 inhibitor, atezolizumab plus BRAFi\/MEKi combination of vemurafenib\/cobimetinib, with placebo plus vemurafenib\/cobimetinb, the addition of immunotherapy to targeted therapy demonstrated a PFS benefit of 5 months. In July 2020, the United States Food and Drug Administration (FDA) approved this combination for the first-line treatment of patients with <em>BRAF-<\/em>V600 unresectable, mutation-positive advanced melanoma. For more details on this approval see <a href=\"https:\/\/aceoncology.org\/#aceoncoblog\/FDA-approvals-July-2020\" rel=\"noreferrer noopener\" target=\"_blank\">ACE OncoBlog<\/a>, 14 August.&nbsp;<\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p><strong>Reference<\/strong><\/p>\n\n\n\n<p>Puzanov I, et al. <em>JAMA Oncology<\/em> 2020; 6(8):1256-1264<\/p>\n","protected":false},"excerpt":{"rendered":"<p>The treatment landscape for patients with advanced (unr [&hellip;]<\/p>\n","protected":false},"author":434,"featured_media":706,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[2],"tags":[],"class_list":["post-1276","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-2"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.8 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Insights on Treatment Sequencing in Advanced BRAF-mutant Melanoma - 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