Developments in the Space of New MAPK Pathway Inhibitors for BRAF-Mutant Melanoma

被引:43
作者
Cohen, Justine, V [1 ]
Sullivan, Ryan J. [1 ]
机构
[1] Harvard Med Sch, Ctr Melanoma, Massachusetts Gen Hosp, Dept Med,Div Med Oncol,Canc Ctr, Boston, MA 02115 USA
关键词
DABRAFENIB PLUS TRAMETINIB; ACQUIRED-RESISTANCE; OPEN-LABEL; RAF INHIBITORS; MEK INHIBITION; TUMOR MICROENVIRONMENT; TARGETED THERAPY; DOSE-ESCALATION; HIGH-RISK; PHASE-II;
D O I
10.1158/1078-0432.CCR-18-0836
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The characterization of the MAPK signaling pathway has led to the development of multiple promising targeted therapy options for a subset of patients with metastatic melanoma. The combination of BRAF and MEK inhibitors represents an FDA-approved standard of care in patients with metastatic and resected BRAF-mutated melanoma. There are currently three FDA-approved BRAF/MEK inhibitor combinations for the treatment of patients with BRAF-mutated melanoma. Although there have been significant advances in the field of targeted therapy, further exploration of new targets within the MAPK pathway will strengthen therapeutic options for patients. Important clinical and translational research focuses on mechanisms of resistance, predictive biomarkers, and challenging patient populations such as those with brain metastases or resected melanoma.
引用
收藏
页码:5735 / 5742
页数:8
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