Zhang Yaxiong, Miao Siyu, Wang Fang, Fang Wenfeng, Chen Gang, Chen Xi, Yan Fang, Huang Xiaodan, Wu Manli, Huang Yan, Zhang Li
Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou 510060, China.
State Key Laboratory of Oncology in South China, Guangzhou 510080, China.
J Thorac Dis. 2017 Jul;9(7):1980-1987. doi: 10.21037/jtd.2017.06.08.
The first generation epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs), gefitinib and erlotinib, have become the standard first-line treatment for non-small-cell lung cancer (NSCLC) patients with EGFR mutation. However, there was no pooled analysis focused on the usage of the second-generation TKI, afatinib, in advanced EGFR-positive NSCLC patients after failure of first generation TKIs. Therefore, a meta-analysis was conducted to solve the above question.
Electronic databases were searched for eligible literatures. ORR (objective response rate), DCR (disease controlled rate), PFS (progression-free survival), OS (overall survival) and primary grade 3/4 adverse events were pooled with the corresponding 95% confidence interval using R software. Sensitivity analyses and heterogeneity were quantitatively evaluated.
A total of 545 EGFR-positive patients were available for analysis from five studies after detailed screening from 909 relevant studies. The pooled ORR and DCR of afatinib in EGFR-positive patients after failure of the first generation EGFR-TKIs were 0.12 (0.08-0.19) and 0.60 (0.53-0.68), respectively. Besides, the 6 m-PFS rate, 1 y-PFS rate and 6 m-OS rate were 0.26 (0.22-0.30), 0.08 (0.06-0.10) and 0.74 (0.56-0.86). The grade 3/4 rate of diarrhea and that of skin deformity were 0.23 (0.10-0.46) and 0.14 (0.05-0.33), respectively. Sensitivity analyses revealed similar results with lower heterogeneity.
Considering the efficacy, toxicity and current availability, afatinib could be a therapeutic option for advanced EGFR mutated NSCLC patients after the failure of 1st-generation TKIs.
第一代表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)吉非替尼和厄洛替尼已成为表皮生长因子受体(EGFR)突变的非小细胞肺癌(NSCLC)患者的标准一线治疗药物。然而,尚无关于第二代TKI阿法替尼在第一代TKI治疗失败后的晚期EGFR阳性NSCLC患者中应用情况的汇总分析。因此,进行了一项荟萃分析以解决上述问题。
检索电子数据库以获取符合条件的文献。使用R软件将客观缓解率(ORR)、疾病控制率(DCR)、无进展生存期(PFS)、总生存期(OS)和主要3/4级不良事件及其相应的95%置信区间进行汇总。对敏感性分析和异质性进行定量评估。
在对909项相关研究进行详细筛选后,共有来自5项研究的545例EGFR阳性患者可供分析。第一代EGFR-TKI治疗失败后,阿法替尼在EGFR阳性患者中的汇总ORR和DCR分别为0.12(0.08-0.19)和0.60(0.53-0.68)。此外,6个月无进展生存率、1年无进展生存率和6个月总生存率分别为0.26(0.22-0.30)、0.08(0.06-0.10)和0.74(0.56-0.86)。腹泻和皮肤畸形的3/4级发生率分别为0.23(0.10-0.46)和0.14(0.05-0.33)。敏感性分析显示结果相似且异质性较低。
考虑到疗效、毒性和当前可用性,阿法替尼可能是第一代TKI治疗失败后的晚期EGFR突变NSCLC患者的一种治疗选择。