聚焦 Amivantamab(JNJ-61186372)治疗表皮生长因子受体外显子 20 插入阳性非小细胞肺癌。

IF 5.1 Q1 ONCOLOGY
Lung Cancer: Targets and Therapy Pub Date : 2021-12-02 eCollection Date: 2021-01-01 DOI:10.2147/LCTT.S337861
Danielle Brazel, Misako Nagasaka
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引用次数: 0

摘要

非小细胞肺癌(NSCLC)患者表现出致癌驱动基因突变的敏感性,已从靶向治疗中获得临床获益。表皮生长因子受体突变可持续激活信号通路,产生促生存和抗凋亡信号。典型的致敏表皮生长因子受体突变,如19号外显子缺失和21号外显子L858R点突变,对酪氨酸激酶抑制剂(TKIs)反应良好。另一方面,4%-12%的表皮生长因子受体突变 NSCLC 会出现表皮生长因子受体 20 外显子框架内插入突变,并且对 TKIs 靶向治疗产生耐药性。2021 年 5 月,美国联邦药品管理局(FDA)加速批准了阿米万他单抗(Rybrevant)用于铂类化疗后出现表皮生长因子受体外显子 20 插入突变的局部晚期或转移性 NSCLC 成人患者。在此,我们将讨论阿米万他单抗的特性、临床试验结果以及表皮生长因子受体外显子 20 插入突变 NSCLC 患者的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spotlight on Amivantamab (JNJ-61186372) for EGFR Exon 20 Insertions Positive Non-Small Cell Lung Cancer.

Spotlight on Amivantamab (JNJ-61186372) for EGFR Exon 20 Insertions Positive Non-Small Cell Lung Cancer.

Spotlight on Amivantamab (JNJ-61186372) for EGFR Exon 20 Insertions Positive Non-Small Cell Lung Cancer.

Non-small cell lung cancer (NSCLC) patients demonstrating sensitizing oncogenic driver mutations have derived clinical benefit from targeted therapy. EGFR mutations constitutively activate the signaling pathway, leading to prosurvival and antiapoptotic signals. Classic sensitizing EGFR mutations, such as exon 19 deletions and exon 21 L858R point mutations, respond well to tyrosine kinase inhibitors (TKIs). On the other hand, EGFR exon 20 in-frame insertions are observed in 4-12% of EGFR-mutated NSCLC and are resistant to targeted therapy with TKIs. In May 2021, the Federal Drug Administration (FDA) provided accelerated approval to amivantamab (Rybrevant) in adults with locally advanced or metastatic NSCLC with EGFR exon 20 insertion mutations after treatment with platinum-based chemotherapy. Here, we discuss properties of amivantamab, clinical trial results, and management of patients with EGFR exon 20 insertion mutated NSCLC.

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来源期刊
CiteScore
8.10
自引率
0.00%
发文量
10
审稿时长
16 weeks
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