The potential of BRAF-targeted therapy combined with immunotherapy in melanoma

被引:9
|
作者
Naderi-Azad, Sheida [1 ]
Sullivan, Ryan [2 ]
机构
[1] Univ Toronto, Fac Med, Toronto, ON, Canada
[2] Massachusetts Gen Hosp, Canc Ctr, Ctr Melanoma, Boston, MA 02114 USA
关键词
BRAF; immunotherapy; melanoma; PD-1; PD-L1; combination therapy; T-CELL RECOGNITION; IMPROVED SURVIVAL; MEK INHIBITION; VEMURAFENIB; BRAF(V600E); DABRAFENIB; PHASE-3; COMBINATION; COBIMETINIB; TRAMETINIB;
D O I
10.1080/14737140.2020.1724097
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Immune checkpoint inhibitor therapy and BRAF-targeted therapy have been developed for the treatment of metastatic melanoma. The optimal use of these agents, either in sequence or combination, for the 40-50% of melanoma patients whose tumors harbor a BRAFV600 mutation is unknown, but data from a number of clinical trials, including one randomized Phase II study, are emerging. Areas covered: This review describes the preclinical and clinical rationale for combined BRAF-targeted therapy with immunotherapy, including the known effects of BRAF-targeted therapy on the immune microenvironment, and the clinical trial data from a number of studies. Expert opinion: BRAF-targeted therapy is associated with high response rates in patients with metastatic melanoma but also leads to changes in the tumor microenvironment that may sensitize these tumors to immunotherapy. The early trials of BRAF-targeted therapy with immunotherapy, in particular with anti-PD-1/PD-L1 agents, are encouraging and suggest that some patients may benefit from this treatment approach. However, incorporating these combinations into routine clinical practice requires the read-out from two randomized clinical trials expected in the coming 1-2 years.
引用
收藏
页码:131 / 136
页数:6
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