Targeted therapy for melanoma: rational combinatorial approaches

被引:68
|
作者
Kwong, L. N. [1 ]
Davies, M. A. [2 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77054 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Melanoma Med Oncol, Houston, TX 77054 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77054 USA
关键词
melanoma; targeted therapy; BRAF; NRAS; DOSE-ESCALATION; MEK INHIBITION; PHASE-I; METASTATIC MELANOMA; ACQUIRED-RESISTANCE; IMPROVED SURVIVAL; KINASE INHIBITOR; RAF INHIBITORS; MUTANT BRAF; CELL-DEATH;
D O I
10.1038/onc.2013.34
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The treatment of melanoma, the most aggressive form of skin cancer, is being revolutionized by the development of personalized targeted therapy approaches. Mutant-selective BRAF inhibitors and MEK inhibitors have demonstrated impressive clinical results in molecularly selected patients. However, emerging understanding of the molecular heterogeneity of this disease and the identification of multiple mechanisms of resistance to targeted therapies strongly support the rationale for combinatorial approaches. In this review, we will discuss the preclinical and clinical studies that are testing leading hypotheses and emerging combinatorial strategies for the future.
引用
收藏
页码:1 / 9
页数:9
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