奥西默替尼
医学
肺癌
癌症研究
突变体
表皮生长因子受体
内科学
肿瘤科
癌症
埃罗替尼
生物
基因
生物化学
作者
Byoung Chul Cho,Enriqueta Felip,Hidetoshi Hayashi,Michael Thomas,Shun Lü,Benjamin Besse,Tao Sun,Melissa Martínez,Seema Sethi,S. Martin Shreeve,Alexander I. Spira
出处
期刊:Future Oncology
[Future Medicine]
日期:2021-12-16
卷期号:18 (6): 639-647
被引量:58
标识
DOI:10.2217/fon-2021-0923
摘要
Third-generation EGFR tyrosine kinase inhibitors (TKIs), such as osimertinib, have demonstrated efficacy in patients with EGFR-mutant non-small-cell lung cancer; however, almost all patients will eventually relapse. Amivantamab is an EGFR-MET bispecific antibody with immune cell-directing activity that targets activating and resistance EGFR mutations and MET mutations and amplifications. In the ongoing CHRYSALIS study (NCT02609776), amivantamab in combination with lazertinib, a potent, brain-penetrant third-generation EGFR TKI, demonstrated antitumor activity in the treatment-naive and osimertinib-relapsed setting. Here the authors present the methodology for the MARIPOSA study (NCT04487080), a phase 3, multicenter, randomized study designed to compare the efficacy and safety of amivantamab and lazertinib combination therapy versus single-agent osimertinib as first-line treatment for EGFR-mutant non-small-cell lung cancer.
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