Division of Pulmonology and Critical Care Medicine, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
Cancer Res Treat. 2023 Jan;55(1):112-122. doi: 10.4143/crt.2022.381. Epub 2022 Jul 19.
Although osimertinib is the standard-of-care treatment of epidermal growth factor receptor (EGFR) T790M mutation-positive non-small cell lung cancer, real-world evidence on the efficacy of osimertinib is not enough to reflect the complexity of the entire course of treatment. Herein, we report on the use of osimertinib in patients with EGFR T790M mutation-positive non-small cell lung cancer who had previously received EGFR tyrosine kinase inhibitor (TKI) treatment in Korea.
Patients with confirmed EGFR T790M after disease progression of prior EGFR-TKI were enrolled and administered osimertinib 80 mg daily. The primary effectiveness outcome was progression-free survival, with time-to-treatment discontinuation, treatment and adverse effects leading to treatment discontinuation, and overall survival being the secondary endpoints.
A total of 558 individuals were enrolled, and 55.2% had investigator-assessed responses. The median progression-free survival was 14.2 months (95% confidence interval [CI], 13.0 to 16.4), and the median time-to-treatment discontinuation was 15.0 months (95% CI, 14.1 to 15.9). The median overall survival was 36.7 months (95% CI, 30.9 to not reached). The benefit with osimertinib was consistent regardless of the age, sex, smoking history, and primary EGFR mutation subtype. However, hepatic metastases at the time of diagnosis, the presence of plasma EGFR T790M, and the shorter duration of prior EGFR-TKI treatment were poor predictors of osimertinib treatment. Ten patients (1.8%), including three with pneumonitis, had to discontinue osimertinib due to severe adverse effects.
Osimertinib demonstrated its clinical effectiveness and survival benefit for EGFR T790M mutation-positive in Korean patients with no new safety signals.
虽然奥希替尼是表皮生长因子受体(EGFR)T790M 突变阳性非小细胞肺癌的标准治疗方法,但奥希替尼疗效的真实世界证据还不足以反映整个治疗过程的复杂性。在此,我们报告了在韩国接受过 EGFR 酪氨酸激酶抑制剂(TKI)治疗后疾病进展的 EGFR T790M 突变阳性非小细胞肺癌患者中使用奥希替尼的情况。
纳入经确认存在 EGFR T790M 突变且先前的 EGFR-TKI 治疗后疾病进展的患者,并给予奥希替尼 80mg 每日一次治疗。主要有效性结局是无进展生存期,次要结局包括治疗终止时间、因治疗和不良反应而导致治疗终止、以及总生存期。
共纳入 558 例患者,其中 55.2%的患者经研究者评估有应答。无进展生存期的中位值为 14.2 个月(95%置信区间[CI],13.0 至 16.4),治疗终止时间的中位值为 15.0 个月(95%CI,14.1 至 15.9)。总生存期的中位值为 36.7 个月(95%CI,30.9 至未达到)。奥希替尼的获益与患者的年龄、性别、吸烟史和原发 EGFR 突变亚型无关。然而,诊断时存在肝转移、血浆 EGFR T790M 阳性以及先前 EGFR-TKI 治疗时间较短是奥希替尼治疗效果不佳的预测因素。10 例患者(1.8%)因严重不良反应而不得不停止奥希替尼治疗,其中包括 3 例肺炎。
奥希替尼在韩国 EGFR T790M 突变阳性的患者中表现出了临床疗效和生存获益,且未出现新的安全性信号。