Suppr超能文献

BRAF 突变型晚期黑色素瘤的一线治疗:一种方法适合所有患者吗?

First line treatment of BRAF mutated advanced melanoma: Does one size fit all?

机构信息

European Institute of Oncology, IRCCS, 20141 Milan, Italy; Department of Oncology and Hematology (DIPO), University of Milan, 20122 Milan, Italy.

European Institute of Oncology, IRCCS, 20141 Milan, Italy.

出版信息

Cancer Treat Rev. 2021 Sep;99:102253. doi: 10.1016/j.ctrv.2021.102253. Epub 2021 Jun 18.

Abstract

In the last decade, immunotherapy and target therapy have revolutionized the prognosis of patients with BRAF-V600 mutation-positive metastatic melanoma. To date, three different combinations of BRAF/MEK inhibitors have been approved for this population, showing comparable efficacy and unique toxicity profiles. Several immune-checkpoint inhibitors, including pembrolizumab, nivolumab and the combination of nivolumab plus ipilimumab, are also available options for untreated metastatic melanoma patients. A novel approach has emerged by combining immune-checkpoint inhibitors and targeted agents, based on preclinical hints of synergy, prompting clinical results from large randomized trials. Specifically, the triplet of atezolizumab, vemurafenib and cobimetinib has been recently approved by FDA for patients with untreated BRAF-mutant metastatic melanoma. With a wide variety of available treatment options in this setting, it is paramount to establish criteria to select the most effective and safe frontline tailored approaches, for each patient. Results from ongoing studies are awaited, to maximise the benefits in survival outcomes and quality of life for patients, balancing adverse events and clinical benefit. The purpose of this review is to summarize the current landscape of standard and experimental treatment strategies for the first line treatment of patients with BRAF-mutated advanced melanoma and discuss the best patient-centered tailored strategies in the first-line setting.

摘要

在过去的十年中,免疫疗法和靶向疗法彻底改变了 BRAF-V600 突变阳性转移性黑色素瘤患者的预后。迄今为止,已有三种不同的 BRAF/MEK 抑制剂联合方案获批用于这一人群,它们具有相似的疗效和独特的毒性特征。几种免疫检查点抑制剂,包括 pembrolizumab、nivolumab 以及 nivolumab 联合 ipilimumab,也是未经治疗的转移性黑色素瘤患者的可选方案。一种新的方法是根据协同作用的临床前提示,将免疫检查点抑制剂与靶向药物联合使用,这促使了来自大型随机试验的临床结果。具体来说,atezolizumab、vemurafenib 和 cobimetinib 的三联疗法最近已被 FDA 批准用于未经治疗的 BRAF 突变转移性黑色素瘤患者。在这种情况下,有各种各样的治疗选择,为每个患者建立最有效和安全的一线个体化方法的标准至关重要。正在进行的研究结果有待公布,以最大限度地提高患者生存结果和生活质量的获益,同时平衡不良反应和临床获益。本综述的目的是总结 BRAF 突变型晚期黑色素瘤一线治疗的标准和实验治疗策略的现状,并讨论一线治疗中最佳的以患者为中心的个体化策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验