Stepwise prolongation of overall survival from first to third generation EGFR-TKIs for EGFR mutation-positive non-small-cell lung cancer: the Tokushukai REAl-world Data project (TREAD 01)

医学 吉非替尼 阿法替尼 埃罗替尼 内科学 肿瘤科 肺癌 盐酸厄洛替尼 置信区间 比例危险模型 奥西默替尼 性能状态 回顾性队列研究 表皮生长因子受体 癌症
作者
Kiyoaki Uryu,Yoshinori Imamura,Rai Shimoyama,T. Mase,Yoshiaki Fujimura,Maki Hayashi,Megu Ohtaki,Keiko Otani,Makoto Hibino,Shigeto Horiuchi,Tomoya Fukui,Ryuta Fukai,Yusuke Chihara,Akihiko Iwase,Noriko Yamada,Yukihiro Tamura,Hiromasa Harada,Nobuaki Shinozaki,Asuka Tsuya,Masahiro Fukuoka,Hironobu Minami
出处
期刊:Japanese Journal of Clinical Oncology [Oxford University Press]
卷期号:54 (3): 319-328 被引量:3
标识
DOI:10.1093/jjco/hyad162
摘要

Abstract Objective The introduction of new-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) has afforded promising overall survival outcomes in clinical trials for non-small-cell lung cancer. We aim to investigate the current adoption rate of these agents and the real-world impact on overall survival among institutions. Methods In a nationwide retrospective cohort study of 46 Tokushukai Medical Group hospitals in Japan, we analyzed clinical data of consecutive patients with non-small-cell lung cancer receiving EGFR-TKIs between April 2010 and March 2020. Univariate and multivariate Cox regression analyses examined the associations between overall survival and patient/tumor-related factors and first-line EGFR-TKIs. Results A total of 758 patients (58.5% females; median age, 73 years) were included. Of 40 patients diagnosed in 2010, 72.5% received gefitinib, whereas 81.3% of 107 patients diagnosed in 2019 received osimertinib as the first-line EGFR-TKI. With a median follow-up of 15.8 months, the median overall survival was 28.4 months (95% confidence interval, 15.3–31.0). In a multivariate Cox regression analysis, age, body mass index, disease status, EGFR mutational status and first-line epidermal growth factor receptor tyrosine kinase inhibitor were identified as significant prognostic factors after adjusting for background factors including study period, hospital volume and hospital type. The estimated 2-year overall survival rates for gefitinib, erlotinib, afatinib and osimertinib were 70.1% (95% confidence interval 59.7–82.4), 67.8% (95% confidence interval 55.3–83.2), 75.5% (95% confidence interval 64.7–88.0) and 90.8% (95% confidence interval 84.8–97.3), respectively. The median time to treatment failure of gefitinib, erlotinib, afatinib and osimertinib were 12.8, 8.8, 12.0 and 16.9 months or more, respectively. Conclusions Our real-world data revealed that the swift and widespread utilization of newer-generation EGFR-TKIs in patients with EGFR mutation-positive non-small-cell lung cancer, and that these newer-generation EGFR-TKIs can prolong overall survival regardless of hospital volume or type. Therefore, osimertinib could be a reasonable first choice treatment for these patients across various clinical practice settings.

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