1. Real-world evidence of osimertinib in Chinese patients with EGFR T790M-positive non-small cell lung cancer: a subgroup analysis from ASTRIS study.
- Author
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Zhou, Qing, Zhang, He-Long, Jiang, Li-Yan, Shi, Yuan-Kai, Chen, Yuan, Yu, Jin-Ming, Zhou, Cai-Cun, He, Yong, Hu, Yan-Ping, Liang, Zong-An, Pan, Yue-Yin, Zhuo, Wen-Lei, Song, Yong, Wu, Gang, Chen, Gong-Yan, Lu, You, Zhang, Cui-Ying, Zhang, Yi-Ping, Cheng, Ying, and Lu, Shun
- Subjects
NON-small-cell lung carcinoma ,CHINESE people ,EPIDERMAL growth factor receptors ,MIGRAINE aura ,OSIMERTINIB ,INTERSTITIAL lung diseases ,SUBGROUP analysis (Experimental design) - Abstract
Purpose: ASTRIS study aimed the largest to evaluate the effectiveness and safety of second- or higher-line osimertinib in patients with advanced/metastatic epidermal growth factor receptor (EGFR) T790M mutation-positive non–small cell lung cancer (NSCLC) in the real-world setting. Here we report the results of Chinese patients in ASTRIS study. Methods: Adults with EGFR T790M-positive advanced NSCLC pretreated with EGFR-tyrosine kinase inhibitor (EGFR-TKI), having a WHO performance status score of 0–2 and asymptomatic, stable central nervous system (CNS) metastases were included. All patients received once-daily osimertinib 80 mg orally. The outcomes included investigator-assessed clinical response, progression-free survival (PFS), time-to-treatment discontinuation (TTD), and safety. Results: A total of 1350 patients were included. Response rate was 55.7% (95% confidence interval [CI] 0.53–0.58). The median PFS and the median TTD were 11.7 months (95% CI 11.1–12.5) and 13.9 months (95% CI 13.1–15.2), respectively. Overall, 389 patients (28.8%) had at least one protocol-specified adverse event (AE); AEs of interstitial lung diseases/pneumonitis-like events and QT prolongation were reported in 3 (0.2%) and 59 (4.4%) patients, respectively. Conclusion: Osimertinib was effective in Chinese patients with T790M-positive NSCLC who had progressed after first- or second-generation EGFR-TKI in real-word setting and the results were consistent with ASTRIS study overall population and AURA studies. No new safety signals or events were identified. Clinical trial number: NCT02474355. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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