Cheema Parneet, Cho Byoung Chul, Freitas Helano, Provencio Mariano, Chen Yuh Min, Kim Sang-We, Wu Yi-Long, Passaro Antonio, Martin Claudio, Tiseo Marcello, Chang Gee-Chen, Park Keunchil, Solomon Benjamin, Burghuber Otto, Laskin Janessa, Wang Ziping, Lee Sung Yong, Hu Yanping, Vansteenkiste Johan, Zhang He-Long, Hanrahan Emer, Geldart Thomas, Taylor Rosemary, Servidio Leslie, Li Jingyi, Marinis Filippo de
William Osler Health System, University of Toronto, Toronto, ON, L6R 3J7, Canada.
Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Future Oncol. 2023 Jan;19(1):61-75. doi: 10.2217/fon-2022-0919. Epub 2023 Jan 19.
Report the final analysis from ASTRIS, the largest real-world study of second-/later-line osimertinib in advanced/metastatic EGFR T790M non-small-cell lung cancer (NSCLC). Patients with advanced/metastatic EGFR T790M NSCLC and prior EGFR-TKI treatment, received once-daily osimertinib 80 mg. Primary end point: overall survival (OS); secondary end points: progression-free survival (PFS), time-to-treatment discontinuation (TTD) and response rate. Safety was also recorded. In 3014 patients, median OS: 22.8 months (21.6-23.8), median PFS: 11.1 months (11.0-12.0), median TTD: 13.5 months (12.6-13.9), and response rate: 57.3% (55.5-59.2). All end points reported with 95% CIs. Numerically longer median OS was observed in patients with baseline WHO performance status <2 versus 2 (24.0 vs 11.1 months) and those without versus with brain/leptomeningeal metastases (25.4 vs 18.0 months). No new safety signals were identified. Second-/later-line osimertinib demonstrated real-world clinical benefit and safety in advanced/metastatic EGFR T790M NSCLC. NCT02474355 (ClinicalTrials.gov).
报告ASTRIS的最终分析结果,这是关于奥希替尼用于晚期/转移性EGFR T790M非小细胞肺癌(NSCLC)二线及以上治疗的最大规模真实世界研究。晚期/转移性EGFR T790M NSCLC患者且既往接受过EGFR-TKI治疗,接受每日一次80mg奥希替尼治疗。主要终点:总生存期(OS);次要终点:无进展生存期(PFS)、治疗中断时间(TTD)和缓解率。同时记录安全性。3014例患者中,中位OS为22.8个月(21.6 - 23.8),中位PFS为11.1个月(11.0 - 12.0),中位TTD为13.5个月(12.6 - 13.9),缓解率为57.3%(55.5 - 59.2)。所有终点均报告了95%置信区间。WHO基线体能状态<2分的患者与体能状态为2分的患者相比,以及无脑/软脑膜转移的患者与有脑/软脑膜转移的患者相比,观察到的中位OS在数值上更长(分别为24.0个月对11.1个月以及25.4个月对18.0个月)。未发现新的安全信号。二线及以上奥希替尼在晚期/转移性EGFR T790M NSCLC中显示出真实世界的临床获益和安全性。NCT02474355(ClinicalTrials.gov)