Advanced Melanoma Resistance Mechanisms to Current Therapies

被引:8
作者
Haugh, Alexandra M. [1 ]
Salama, April K. S. [2 ]
Johnson, Douglas B. [3 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Med, 719 Thompson Lane,Suite 20400, Nashville, TN 37204 USA
[2] Duke Univ, Med Ctr, Dept Med, 20 Duke Med Cir, Durham, NC 27710 USA
[3] Vanderbilt Univ, Med Ctr, Vanderbilt Ingram Canc Ctr, Dept Med, 777 PRB,2220 Pierce Ave, Nashville, TN 37232 USA
关键词
Immune checkpoint inhibitor; Immunotherapy; Resistance; BRAF inhibitor; MEK inhibitor; Melanoma; BRAF INHIBITOR RESISTANCE; IMMUNE CHECKPOINT BLOCKADE; ADVANCED BRAF(V600)-MUTANT MELANOMA; EXOME ANALYSIS REVEALS; PD-1; BLOCKADE; ACQUIRED-RESISTANCE; TUMOR MICROENVIRONMENT; T-CELLS; BRAF(V600E) INHIBITION; NEOANTIGEN LANDSCAPE;
D O I
10.1016/j.hoc.2020.09.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Novel therapeutic agents introduced over the past decade, including immune checkpoint inhibitors and targeted therapies, have revolutionized the management of metastatic melanoma and significantly improved patient outcomes. Although robust and durable responses have been noted in some cases, treatment is often limited by innate or acquired resistance to these agents. This article provides an overview of known and suspected mechanisms involved with acquired resistance to BRAF/MEK inhibitors as well as developing insights into innate and acquired resistance to checkpoint inhibitors in patients with melanoma. © 2020 Elsevier Inc.
引用
收藏
页码:111 / 128
页数:18
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