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奥希替尼之外:第三代 EGFR 酪氨酸激酶抑制剂在晚期 EGFR+ NSCLC 中的研发进展

Beyond Osimertinib: The Development of Third-Generation EGFR Tyrosine Kinase Inhibitors For Advanced EGFR+ NSCLC.

机构信息

Department of Oncology, Karmanos Cancer Institute, Wayne State University School of Medicine, Detroit, Michigan; Division of Neurology, Department of Internal Medicine, St. Marianna University, Kawasaki, Kanagawa, Japan.

Division of Hematology/Oncology, Department of Medicine, Chao Family Comprehensive Cancer Center, University of California Irvine School of Medicine, Orange, California.

出版信息

J Thorac Oncol. 2021 May;16(5):740-763. doi: 10.1016/j.jtho.2020.11.028. Epub 2020 Dec 15.

Abstract

Single-agent osimertinib is the standard of care for the first-line treatment of advancedEGFR+ NSCLC and remained the only marketed third-generation EGFR tyrosine kinase inhibitor (TKI) until March 2020 when almonertinib (HS-10296) was approved in the People's Republic of China for the treatment of advanced EGFR T790M+ NSCLC based on a phase 2 expansion study of a phase 1/2 trial. In this review, we profiled many of the third-generation EGFR TKIs in late-stage clinical development (e.g., almonertinib, lazertinib, alflutinib, rezivertinib, ASK120069, SH-1028, D-0316, and abivertinib) based on their interim results from phase 1 and phase 2 trials, and included the designs of the phase 3 trials and their chemical structures when publicly available. We also listed other third-generation EGFR TKIs in pipeline development based on the search of clinical trial registration websites. In addition, we summarized the results of clinical trials that previously reported third-generation EGFR TKIs (rociletinib, olmutinib, nazartinib, mavelertinib), including phase 3 results of rociletinib and naquotinib. We further profiled combination clinical trial design of the third-generation EGFR TKIs including FLAURA2 (NCT04035486), MARIPOSA (NCT04487080), ACROSS1 (NCT04500704), and ACROSS2 (NCT04500717) that if positive can potentially usher in the next standard of care for advanced EGFR+ NSCLC.

摘要

奥希替尼单药是治疗晚期 EGFR+ NSCLC 的标准一线治疗药物,直到 2020 年 3 月,阿美替尼(HS-10296)在中国获批用于治疗晚期 EGFR T790M+ NSCLC,才成为唯一上市的第三代 EGFR 酪氨酸激酶抑制剂(TKI)。该药物是基于一项 1/2 期研究的 2 期扩展研究获批,成为晚期 EGFR+ NSCLC 的新标准。在这篇综述中,我们根据 1 期和 2 期试验的中期结果,对许多处于晚期临床开发阶段的第三代 EGFR TKI(如阿美替尼、拉泽替尼、阿弗替尼、雷泽替尼、ASK120069、SH-1028、D-0316 和阿维替尼)进行了描述,并在公开时包括了 3 期试验的设计和它们的化学结构。我们还根据临床试验注册网站的搜索列出了其他处于研发阶段的第三代 EGFR TKI。此外,我们总结了之前报道的第三代 EGFR TKI(rociletinib、olmutinib、nazartinib、mavelertinib)的临床试验结果,包括 rociletinib 和 naquotinib 的 3 期结果。我们进一步描述了第三代 EGFR TKI 的联合临床试验设计,包括 FLAURA2(NCT04035486)、MARIPOSA(NCT04487080)、ACROSS1(NCT04500704)和 ACROSS2(NCT04500717),如果这些试验结果为阳性,可能会为晚期 EGFR+ NSCLC 带来下一个标准治疗方案。

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