Department of Internal Medicine, Samsung Medical Center, Seoul, Korea.
Department of Internal Medicine, Kosin University Gospel Hospital, Kosin University College of Medicine, Busan, Korea.
Cancer Res Treat. 2023 Oct;55(4):1152-1170. doi: 10.4143/crt.2023.493. Epub 2023 May 19.
This study aimed to report the final analysis of time-on-treatment (TOT) and overall survival (OS) in patients with advanced-stage epidermal growth factor receptor (EGFR)+ non-small cell lung cancer (NSCLC) who received sequential afatinib and osimertinib and to compare the outcomes with other second-line regimens (comparator group).
In this updated report, the existing medical records were reviewed and rechecked. TOT and OS were updated and analyzed according to clinical features using the Kaplan-Meier method and log-rank test. TOT and OS were compared with those of the comparator group, in which most patients received pemetrexed-based treatments. A multivariable Cox proportional hazard model was used to evaluate features that could affect survival outcomes.
The median observation time was 31.0 months. The follow-up period was extended to 20 months. A total of 401 patients who received first-line afatinib were analyzed (166 with T790M+ and second-line osimertinib, and 235 with unproven T790M and other second-line agents). Median TOTs on afatinib and osimertinib were 15.0 months (95% confidence interval [CI], 14.0 to 16.1) and 11.9 months (95% CI, 8.9 to 14.6), respectively. The median OS in the osimertinib group was 54.3 months (95% CI, 46.7 to 61.9), much longer than that in the comparator group. In patients who received osimertinib, the OS was longest with Del19+ (median, 59.1; 95% CI, 48.7 to 69.5).
This is one of the largest real-world studies reporting the encouraging activity of sequential afatinib and osimertinib in Asian patients with EGFR+ NSCLC who acquired the T790M mutation, particularly Del19+.
本研究旨在报告接受序贯阿法替尼和奥希替尼治疗的晚期表皮生长因子受体(EGFR)+非小细胞肺癌(NSCLC)患者的治疗时间(TOT)和总生存期(OS)的最终分析,并与其他二线治疗方案(对照组)进行比较。
在本更新报告中,回顾并重新检查了现有病历。根据临床特征,使用Kaplan-Meier 方法和对数秩检验更新并分析 TOT 和 OS。将 TOT 和 OS 与对照组进行比较,对照组中大多数患者接受培美曲塞为基础的治疗。使用多变量 Cox 比例风险模型评估可能影响生存结果的特征。
中位观察时间为 31.0 个月。随访时间延长至 20 个月。共分析了 401 例接受一线阿法替尼治疗的患者(166 例 T790M+患者,二线奥希替尼治疗;235 例 T790M 未知患者,接受其他二线药物治疗)。阿法替尼和奥希替尼的中位 TOT 分别为 15.0 个月(95%CI,14.0 至 16.1)和 11.9 个月(95%CI,8.9 至 14.6)。奥希替尼组的中位 OS 为 54.3 个月(95%CI,46.7 至 61.9),明显长于对照组。在接受奥希替尼治疗的患者中,Del19+患者的 OS 最长(中位,59.1;95%CI,48.7 至 69.5)。
这是报告接受 T790M 突变(尤其是 Del19+)的亚洲 EGFR+ NSCLC 患者序贯阿法替尼和奥希替尼治疗具有令人鼓舞疗效的最大真实世界研究之一。