奥西默替尼
T790米
肺癌
中止
医学
表皮生长因子受体
肿瘤科
内科学
抗性突变
癌症研究
酪氨酸激酶抑制剂
化疗
癌症
生物
埃罗替尼
基因
吉非替尼
遗传学
聚合酶链反应
逆转录酶
作者
Juliann Chmielecki,Tony S.K. Mok,Yi-Long Lung Cancer Wu,Ji‐Youn Han,Myung‐Ju Ahn,Suresh S. Ramalingam,Thomas John,Isamu Okamoto,James Chih‐Hsin Yang,Frances Alice Shepherd,Krishna C. Bulusu,Gianluca Laus,Barbara Collins,J. Carl Barrett,Ryan James Hartmaier,Vassiliki A. Papadimitrakopoulou
标识
DOI:10.1038/s41467-023-35962-x
摘要
Osimertinib, an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI), potently and selectively inhibits EGFR-TKI-sensitizing and EGFR T790M resistance mutations. This analysis evaluates acquired resistance mechanisms to second-line osimertinib (n = 78) in patients with EGFR T790M advanced non-small cell lung cancer (NSCLC) from AURA3 (NCT02151981), a randomized phase 3 study comparing osimertinib with chemotherapy. Plasma samples collected at baseline and disease progression/treatment discontinuation are analyzed using next-generation sequencing. Half (50%) of patients have undetectable plasma EGFR T790M at disease progression and/or treatment discontinuation. Fifteen patients (19%) have >1 resistance-related genomic alteration; MET amplification (14/78, 18%) and EGFR C797X mutation (14/78, 18%).
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