Cabozantinib Response in a Patient With NSCLC Harboring Both MET Exon 14 Skipping Mutation and Secondary RET Fusion: A Case Report

IF 3 Q2 ONCOLOGY
Carlos Torrado MD , Jamie Feng MD, FRCPC , Elizabeth Faour MD, FRCPC , Natasha B. Leighl MD, MMSc, FRCPC, FASCO
{"title":"Cabozantinib Response in a Patient With NSCLC Harboring Both MET Exon 14 Skipping Mutation and Secondary RET Fusion: A Case Report","authors":"Carlos Torrado MD ,&nbsp;Jamie Feng MD, FRCPC ,&nbsp;Elizabeth Faour MD, FRCPC ,&nbsp;Natasha B. Leighl MD, MMSc, FRCPC, FASCO","doi":"10.1016/j.jtocrr.2024.100647","DOIUrl":null,"url":null,"abstract":"<div><p>MET exon 14 skipping mutation has emerged as a new oncogenic driver in NSCLC with available targeted therapies, including Food and Drug Administration–approved inhibitors capmatinib and tepotinib. Potential resistance mechanisms are beginning to be described and include several on-target and off-target mutations. Here, we report an emergent secondary RET fusion in a patient with a primary MET exon 14 skipping mutation that progressed on capmatinib after the initial response. Subsequently, this patient received both a RET inhibitor (selpercatinib) followed by another MET-targeted treatment (tepotinib) without clinical benefit. Thereafter, cabozantinib, a multikinase inhibitor with activity against RET and MET was started with a rapid clinical and radiologic benefit.</p></div>","PeriodicalId":17675,"journal":{"name":"JTO Clinical and Research Reports","volume":"5 4","pages":"Article 100647"},"PeriodicalIF":3.0000,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666364324000171/pdfft?md5=873c3988b4ea93bcebc85f563c2e0064&pid=1-s2.0-S2666364324000171-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JTO Clinical and Research Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666364324000171","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

MET exon 14 skipping mutation has emerged as a new oncogenic driver in NSCLC with available targeted therapies, including Food and Drug Administration–approved inhibitors capmatinib and tepotinib. Potential resistance mechanisms are beginning to be described and include several on-target and off-target mutations. Here, we report an emergent secondary RET fusion in a patient with a primary MET exon 14 skipping mutation that progressed on capmatinib after the initial response. Subsequently, this patient received both a RET inhibitor (selpercatinib) followed by another MET-targeted treatment (tepotinib) without clinical benefit. Thereafter, cabozantinib, a multikinase inhibitor with activity against RET and MET was started with a rapid clinical and radiologic benefit.

卡博替尼对同时携带 MET 第 14 号外显子跳越突变和继发性 RET 融合的 NSCLC 患者的应答:病例报告
MET第14外显子跳越突变已成为NSCLC新的致癌驱动因素,现有的靶向疗法包括美国食品药品管理局批准的抑制剂卡马替尼和泰泊替尼。目前已开始描述潜在的耐药机制,包括几种靶上和靶下突变。在此,我们报告了一名原发性 MET 14 号外显子跳越突变患者出现的继发性 RET 融合,该患者在服用卡马替尼后出现了初步应答,但病情有所进展。随后,该患者同时接受了一种 RET 抑制剂(赛铂替尼)和另一种 MET 靶向治疗(替泊替尼),但均未获得临床获益。此后,该患者开始接受卡博替尼(一种对RET和MET具有活性的多激酶抑制剂)治疗,并迅速获得了临床和放射学疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信