Tsai Ming-Ju, Hung Jen-Yu, Ma Juei-Yang, Tsai Yu-Chen, Wu Kuan-Li, Lee Mei-Hsuan, Kuo Chia-Yu, Chuang Cheng-Hao, Lee Tai-Huang, Lee Yen-Lung, Huang Chun-Ming, Shen Mei-Chiou, Yang Chih-Jen, Chong Inn-Wen
Department of Internal Medicine, Division of Pulmonary and Critical Care Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 80756, Taiwan.
School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
Cancers (Basel). 2023 Mar 28;15(7):2019. doi: 10.3390/cancers15072019.
Afatinib is an irreversible tyrosine kinase inhibitor (TKI) targeting the epidermal growth factor receptor (EGFR), which is utilized for the treatment of patients with advanced lung cancer that harbors mutations. No studies have evaluated the clinical efficacy of LCT in patients treated with first-line afatinib. In this study, we retrospectively enrolled patients with advanced lung adenocarcinomas harboring susceptible mutations who were diagnosed and treated with first-line afatinib in three hospitals. A total of 254 patients were enrolled, including 30 (12%) patients who received LCT (15 patients received definitive radiotherapy for the primary lung mass and 15 patients received curative surgery). Patients who received LCT had a significantly longer PFS than those who did not (median PFS: 32.8 vs. 14.5 months, = 0.0008). Patients who received LCT had significantly longer OS than those who did not (median OS: 67.1 vs. 34.5 months, = 0.0011). Multivariable analysis showed LCT was an independent prognostic factor for improved PFS (adjusted hazard ratio [aHR] [95% confidence interval (CI)]: 0.44 [0.26-0.73], = 0.0016) and OS (aHR [95% CI]: 0.26 [0.12-0.54], = 0.0004). The analyses using propensity score-weighting showed consistent results. We conclude that LCT may improve clinical outcomes, in terms of PFS and OS, in patients with advanced -mutant lung adenocarcinomas who are treated with first-line afatinib.
阿法替尼是一种不可逆的酪氨酸激酶抑制剂(TKI),靶向表皮生长因子受体(EGFR),用于治疗携带特定突变的晚期肺癌患者。尚无研究评估局部巩固治疗(LCT)在接受一线阿法替尼治疗患者中的临床疗效。在本研究中,我们回顾性纳入了在三家医院诊断并接受一线阿法替尼治疗的携带敏感特定突变的晚期肺腺癌患者。共纳入254例患者,其中30例(12%)接受了LCT(15例患者接受了针对原发性肺肿块的根治性放疗,15例患者接受了根治性手术)。接受LCT的患者的无进展生存期(PFS)显著长于未接受LCT的患者(中位PFS:32.8个月对14.5个月,P = 0.0008)。接受LCT的患者的总生存期(OS)显著长于未接受LCT的患者(中位OS:67.1个月对34.5个月,P = 0.0011)。多变量分析显示LCT是改善PFS(调整后风险比[aHR][95%置信区间(CI)]:0.44[0.26 - 0.73],P = 0.0016)和OS(aHR[95%CI]:0.26[0.12 - 0.54],P = 0.0004)的独立预后因素。使用倾向评分加权的分析显示了一致的结果。我们得出结论,对于接受一线阿法替尼治疗的携带特定突变的晚期肺腺癌患者,LCT可能在PFS和OS方面改善临床结局。