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与目前可用的基于突变的靶向疗法相比,比美替尼、恩考芬尼和马西替尼用于治疗黑色素瘤时疗效会更好吗?

Can binimetinib, encorafenib and masitinib be more efficacious than currently available mutation-based targeted therapies for melanoma treatment?

作者信息

Turner Megan C, Rossfeld Kara, Salama April K S, Tyler Douglas, Beasley Georgia

机构信息

a Department of Surgery , Duke University , Durham , NC , USA.

b Department of Surgery , Ohio State University , Columbus , OH , USA.

出版信息

Expert Opin Pharmacother. 2017 Apr;18(5):487-495. doi: 10.1080/14656566.2017.1299710. Epub 2017 Mar 22.

Abstract

Historically, there were few effective and durable treatments for metastatic melanoma. Recently, mutation based targeted therapies have revolutionized treatment and outcomes for patients with metastatic melanoma. Specifically, inhibitors aimed at BRAF, NRAS, and C-KIT mutations are now commonly used in treatment for patients harboring the specific mutations. Areas covered: A brief review of current BRAF, NRAS, and C-KIT inhibitors provides background for a thorough review of newly developed agents namely binimetinib, a MEK inhibitor, encorafenib a BRAF inhibitor, and masitinib which inhibits C-KIT. Expert opinion: While the 3 novel agents reviewed here have potential for use in melanoma, optimal utilization will occur once a more personalized approach incorporating genomic, proteomic, and immunologic data guides therapeutic decisions.

摘要

从历史上看,转移性黑色素瘤几乎没有有效的持久治疗方法。最近,基于突变的靶向治疗彻底改变了转移性黑色素瘤患者的治疗方式和治疗结果。具体而言,针对BRAF、NRAS和C-KIT突变的抑制剂现在常用于治疗携带特定突变的患者。涵盖领域:对当前BRAF、NRAS和C-KIT抑制剂的简要回顾为全面审查新开发的药物提供了背景,这些药物包括MEK抑制剂比美替尼、BRAF抑制剂恩考芬尼以及抑制C-KIT的马西替尼。专家意见:虽然这里审查的3种新型药物有用于黑色素瘤治疗的潜力,但一旦采用结合基因组、蛋白质组和免疫数据的更个性化方法来指导治疗决策,就能实现最佳利用。

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