医学
四分位间距
内科学
子群分析
置信区间
胃肠病学
肿瘤科
作者
Shun Lü,Jian Fang,Xingya Li,Lejie Cao,Jianying Zhou,Qisen Guo,Zongan Liang,Ying Cheng,Liyan Jiang,Nong Yang,Zhigang Han,Jianhua Shi,Yuan Chen,Hua Xu,Helong Zhang,Gongyan Chen,Rui Ma,Sanyuan Sun,Yun Fan,Songhua Fan
标识
DOI:10.1016/j.jtocrr.2022.100407
摘要
Introduction Savolitinib has been found to have encouraging antitumor activity and a favorable safety profile in Chinese patients with pulmonary sarcomatoid carcinoma and other NSCLCs with MET exon 14 skipping alterations ( MET ex14 positive) at the primary analysis of a phase 2 study. Here, we present the long-term efficacy and safety data of savolitinib, including subgroup analyses. Methods This multicenter, single-arm, open-label, phase 2 study in the People's Republic of China enrolled MET inhibitor-naive adults with locally advanced or metastatic MET ex14-positive NSCLC (NCT02897479). Oral savolitinib at a dose of 400 or 600 mg was administered once daily (body weight dependent). The primary objectives of the final analysis were long-term overall survival (OS) and subgroup analyses by previous systemic treatment, NSCLC subtypes, and brain metastases. Results At the final analysis cutoff date (June 28, 2021), a total of 70 patients were enrolled and receiving savolitinib, and median follow-up was 28.4 (interquartile range: 26.2–36.3) months. The median OS was 12.5 months (95% confidence interval [CI]: 10.5–21.4 [18- and 24-mo OS rates, 42.1% and 31.5%, respectively]). Median OS in pretreated or treatment-naive patients was 19.4 (95% CI: 10.5–31.3) and 10.9 (95% CI: 7.5–14.0) months, respectively; it was 10.6 months (95% CI: 4.6–14.0) in patients with pulmonary sarcomatoid carcinoma, 17.3 months (95% CI: 10.6–23.6) in other NSCLC subtypes, and 17.7 months (95% CI: 10.5–not evaluable) in patients with brain metastases. No new safety signals emerged with prolonged follow-up and exposure. Conclusions The updated results further confirm the favorable benefit and acceptable safety of savolitinib in Chinese patients with MET ex14-positive NSCLC.
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