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BRAF和MEK抑制用于治疗晚期BRAF突变型黑色素瘤。

BRAF and MEK inhibition for the treatment of advanced BRAF mutant melanoma.

作者信息

Richman Juliet, Martin-Liberal Juan, Diem Stefan, Larkin James

机构信息

The Royal Marsden Hospital , Fulham Road SW3 6JJ, London , UK +44 20 7811 8576 ; +44 20 7811 8103 ;

出版信息

Expert Opin Pharmacother. 2015 Jun;16(9):1285-97. doi: 10.1517/14656566.2015.1044971.

Abstract

INTRODUCTION

BRAF inhibition alone has achieved unprecedented efficacy results in patients affected by BRAF-mutated advanced melanoma. Since these findings, it was postulated that dual inhibition of BRAF and other components of the RAS/RAF/MEK/ERK MAPK pathway (such as MEK) would be superior to BRAF inhibition as monotherapy. A series of recent clinical trials have confirmed this hypothesis.

AREAS COVERED

In this article, the biological rationale for both single and concomitant inhibitions of the MAPK pathway in BRAF mutant melanoma is provided. Moreover, available clinical data on the efficacy and toxicity of BRAF and MEK inhibition as single agents and in combination are extensively reviewed.

EXPERT OPINION

Dual BRAF and MEK inhibition in advanced BRAF-mutated melanoma is superior to single inhibition in terms of efficacy without significant increase in toxicity. Therefore, BRAF plus MEK inhibition is expected to supersede single-agent BRAF inhibition in these patients in the near future.

摘要

引言

单独使用BRAF抑制剂已在BRAF突变的晚期黑色素瘤患者中取得了前所未有的疗效。自这些发现以来,有人推测BRAF与RAS/RAF/MEK/ERK丝裂原活化蛋白激酶(MAPK)通路的其他成分(如MEK)的双重抑制作用将优于BRAF单药治疗。最近的一系列临床试验证实了这一假设。

涵盖领域

本文阐述了BRAF突变型黑色素瘤中MAPK通路单药抑制和联合抑制的生物学原理。此外,还广泛综述了BRAF和MEK抑制剂单药及联合使用时的疗效和毒性方面的现有临床数据。

专家观点

在晚期BRAF突变型黑色素瘤中,BRAF和MEK双重抑制在疗效方面优于单药抑制,且毒性无显著增加。因此,BRAF加MEK抑制有望在不久的将来取代这些患者的BRAF单药抑制治疗。

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