在RET融合驱动的NSCLC和获得性HER2扩增患者中,将曲妥珠单抗德鲁西替康加入塞尔帕替尼:病例报告

IF 3 Q2 ONCOLOGY
Chetan V. Vakkalagadda MD , Jyoti D. Patel MD
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引用次数: 0

摘要

尽管选择性RET抑制剂在RET驱动的非小细胞肺癌中具有高活性,但最终会产生耐药性,因此需要更好地为患者确定治疗方案。这是一个患者最初被认为没有可靶向的改变,然后发现有RET融合,随后在三个不同的活检中发现HER2扩增。她最初接受化疗和免疫治疗,然后改用selpercatinib,最终在selpercatinib中加入了fama -曲妥珠单抗德鲁西替康。在p53突变的背景下,她在进展过程中也出现了神经内分泌分化,这是一个已知的可导致小细胞转化的因素。该患者的病例强调了在诊断和进展过程中需要进行全面的分子检测,因为可能会发现意想不到的耐药机制,特别是对于具有罕见驱动突变的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Addition of Trastuzumab Deruxtecan to Selpercatinib in a Patient With RET Fusion-Driven NSCLC and an Acquired HER2 Amplification: Case Report

Despite the high activity of selective RET inhibitors in RET-driven NSCLC, resistance eventually develops and there is unmet need to better define therapeutic options for patients. This is a case of a patient initially thought to have no targetable alterations, then found to have a RET fusion, and subsequently HER2 amplification on three distinct biopsies. She was treated initially with chemotherapy and immune therapy, then switched to selpercatinib, and eventually had fam-trastuzumab deruxtecan added to selpercatinib. She also developed neuroendocrine differentiation at time of progression in the context of a p53 mutation, which is a known factor that can lead to small cell transformation. This patient’s case highlights the need for comprehensive molecular testing at both diagnosis and progression, as unexpected resistance mechanisms may be identified particularly for patients with uncommon driver mutations.

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
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