Targeting Non-V600 Mutations in BRAF: A Single Institution Retrospective Analysis and Review of the Literature.

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Drugs in Research & Development Pub Date : 2024-09-01 Epub Date: 2024-08-23 DOI:10.1007/s40268-024-00475-5
Hirra A Chaudhary, Timothy L Cannon, Arthur Winer
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Abstract

Background and objective: While successful treatment paradigms for BRAF V600 mutations have been developed, 10% of BRAF mutations are not at V600 and lack a standard treatment regimen. This study summarizes the current body of knowledge on the treatment of non-V600 mutations and reports a single institution experience.

Methods: We conducted a literature review to summarize relevant preclinical and clinical published data on the response of non-V600 mutations to targeted therapies. We performed a retrospective analysis of INOVA Schar Cancer patients registered in our Molecular Tumor Board database with non-V600 BRAF mutations who were recipients of targeted therapy and assessed their time to next treatment and best response.

Results: Published preclinical and clinical data have demonstrated limiting results in the response of non-V600 mutated cancers to targeted therapies. Response rates were variable for the major classes of BRAF mutations including class II and class III mutations as well as, BRAF fusions. Data collected from our INOVA cohort offered promising results with one patient achieving partial remission and two patients achieving stable disease.

Conclusions: This article reflects the current understanding of targeted therapies in non-V600 mutations. Further large-scale studies separating BRAF mutations based on their mechanism of activation will  expand our understanding.

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靶向 BRAF 中的非 V600 突变:单机构回顾性分析和文献综述。
背景和目的:虽然针对 BRAF V600 基因突变的成功治疗范例已经开发出来,但仍有 10% 的 BRAF 基因突变不属于 V600,缺乏标准治疗方案。本研究总结了当前治疗非 V600 突变的知识体系,并报告了单个机构的经验:我们进行了文献综述,总结了非 V600 突变对靶向治疗反应的相关临床前和临床发表数据。我们对分子肿瘤委员会数据库中登记的接受靶向治疗的非V600 BRAF突变的INOVA沙尔癌症患者进行了回顾性分析,并评估了他们接受下一次治疗的时间和最佳反应:已公布的临床前和临床数据显示,非 V600 突变癌症对靶向疗法的反应效果有限。BRAF突变的主要类别(包括II类和III类突变以及BRAF融合)的反应率各不相同。从我们的INOVA队列中收集的数据提供了有希望的结果,一名患者获得部分缓解,两名患者病情稳定:本文反映了目前对非 V600 突变靶向疗法的理解。根据 BRAF 突变的激活机制对其进行分离的进一步大规模研究将拓展我们的认识。
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来源期刊
Drugs in Research & Development
Drugs in Research & Development Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.10
自引率
0.00%
发文量
31
审稿时长
8 weeks
期刊介绍: Drugs in R&D is an international, peer reviewed, open access, online only journal, and provides timely information from all phases of drug research and development that will inform clinical practice. Healthcare decision makers are thus provided with knowledge about the developing place of a drug in therapy. The Journal includes: Clinical research on new and established drugs; Preclinical research of direct relevance to clinical drug development; Short communications and case study reports that meet the above criteria will also be considered; Reviews may also be considered.
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