Emerging insights into resistance to BRAF inhibitors in melanoma

被引:75
作者
Bucheit, Amanda D. [1 ]
Davies, Michael A. [2 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Canc Med, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
关键词
Melanoma; BRAF inhibitor; Resistance; MAPK; PI3K; CUTANEOUS MELANOMA; RAF INHIBITORS; SELECTIVE INHIBITOR; ACQUIRED-RESISTANCE; SIGNALING PATHWAYS; DRIVEN RESISTANCE; IMPROVED SURVIVAL; MEK INHIBITION; CYCLIN D1; PHASE-II;
D O I
10.1016/j.bcp.2013.11.013
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Melanoma is the most aggressive form of skin cancer. The treatment of patients with advanced melanoma is rapidly evolving due to an improved understanding of molecular drivers of this disease. Somatic mutations in BRAF are the most common genetic alteration found in these tumors. Recently, two different mutant-selective small molecule inhibitors of BRAF, vemurafenib and dabrafenib, have gained regulatory approval based on positive results in randomized phase III trials. While the development of these agents represents a landmark in the treatment of melanoma, the benefit of these agents is limited by the frequent and rapid onset of resistance. The identification of several molecular mechanisms of resistance to BRAF inhibitors is rapidly leading to the clinical testing of combinatorial strategies to improve the clinical benefit of these agents. These mechanisms, and the lessons learned from the initial testing of the BRAF inhibitors, provide multiple insights that may facilitate the development of targeted therapies against other oncogenic mutations in melanoma, as well as in other cancers. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:381 / 389
页数:9
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