医学
T790米
培美曲塞
无容量
埃罗替尼
肺癌
吉非替尼
肿瘤科
阿法替尼
内科学
卡铂
奥西默替尼
抗性突变
盐酸厄洛替尼
表皮生长因子受体
癌症
癌症研究
化疗
免疫疗法
顺铂
生物化学
化学
逆转录酶
基因
核糖核酸
作者
Hidetoshi Hayashi,Yasutaka Chiba,Kazuko Sakai,Tomonobu Fujita,Hiroshige Yoshioka,Daisuke Sakai,Chiyoe Kitagawa,Tateaki Naito,Koji Takeda,Isamu Okamoto,Tetsuya Mitsudomi,Yutaka Kawakami,Kazuto Nishio,Shinichiro Nakamura,Nobuyuki Yamamoto,Kazuhiko Nakagawa
标识
DOI:10.1016/j.cllc.2017.05.012
摘要
Antibodies to programmed cell death–1 (PD-1), such as nivolumab, have shown promising clinical activity in patients with advanced non–small-cell lung cancer (NSCLC), but their efficacy appears to be less pronounced in patients with such tumors harboring epidermal growth factor receptor gene (EGFR) mutations. Recent findings suggest that patients with EGFR mutation–positive NSCLC who develop resistance to tyrosine kinase inhibitors (TKIs) due to mechanisms other than acquisition of the secondary T790M mutation of EGFR are more likely to benefit from nivolumab treatment, possibly as a result of a higher level of expression of the PD-1 ligand PD-L1, than are patients who are T790M-positive. The WJOG8515L study (UMIN ID: 000021133) is a randomized phase II trial to compare nivolumab with the combination of carboplatin and pemetrexed in patients with EGFR mutation–positive nonsquamous NSCLC who have developed resistance to EGFR-TKIs due to mechanisms other than T790M. Eligible patients are those with stage IV or recurrent EGFR mutation–positive NSCLC who experience disease progression after therapy with more than 1 EGFR-TKI, including gefitinib, erlotinib, or afatinib; they must show no evidence of the T790M mutation on analysis of a tumor biopsy specimen obtained after progression on such EGFR-TKI therapy, or, if T790M is detected, they must again experience progression on subsequent treatment with a third-generation EGFR-TKI. The primary endpoint is progression-free survival (PFS), and secondary end points include overall survival (OS), objective response rate, duration of response, safety, and OS and PFS according to PD-L1 expression level. Recruitment started in May 2016 and is ongoing.
科研通智能强力驱动
Strongly Powered by AbleSci AI