Zhang Yaxiong, Chen Gang, Chen Xi, Fang Wenfeng, Gao Fei, Yang Yunpeng, Zhao Yuanyuan, Ma Yuxiang, Hong Shaodong, Zhang Zhonghan, Miao Siyu, Wu Manli, Huang Xiaodan, Luo Youli, Zhou Cong, Gong Run, Huang Yan, Chen Likun, Zhou Ningning, Zhao Hongyun, Zhang Li
Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, China.
Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China.
J Cancer. 2017 Jul 2;8(10):1865-1871. doi: 10.7150/jca.19867. eCollection 2017.
Advanced non-small-cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletion (19 Del) and exon 21 L858R mutation (L858R) might be distinct diseases. Therefore, it is necessary to take EGFR mutation subgroups into consideration for making choices of subsequent treatment after tyrosine kinase inhibitors (TKIs) failure. : 174 patients who developed to EGFR-TKI failure were categorized into three cohorts of dramatic progression, gradual progression and local progression. Chi-square was used to compare the distribution of failure modes between 19 Del and L858R. Kaplan-Meier method and Cox Regression were performed for analyses of survival in different subsequent treatments. The distribution of EGFR-TKI failure modes showed no significant difference between 19 Del and L858R. Patients in gradual progression had a longer progression-free survival (PFS) and overall survival (OS) compared with other failure modes in whole population, 19 Del cohort and L858R cohort. 19 Del patients with dramatic progression would obtain survival benefit from chemotherapy, while those with gradual progression got no survival benefit neither from chemotherapy nor previous TKI continuation. However, patients with dramatic or gradual progression would benefit from previous TKI continuation in L858R cohort. For advanced EGFR-positive NSCLC patients with acquired resistance to EGFR-TKI, subsequent treatment should be personalized according to EGFR-TKI failure modes & EGFR mutation subtypes.
伴有表皮生长因子受体(EGFR)外显子19缺失(19 Del)和外显子21 L858R突变(L858R)的晚期非小细胞肺癌(NSCLC)可能是不同的疾病。因此,在酪氨酸激酶抑制剂(TKIs)治疗失败后选择后续治疗方案时,有必要考虑EGFR突变亚组。174例出现EGFR-TKI治疗失败的患者被分为快速进展、缓慢进展和局部进展三个队列。采用卡方检验比较19 Del和L858R之间治疗失败模式的分布情况。采用Kaplan-Meier法和Cox回归分析不同后续治疗的生存情况。EGFR-TKI治疗失败模式的分布在19 Del和L858R之间无显著差异。与整个人群、19 Del队列和L858R队列中的其他治疗失败模式相比,缓慢进展的患者无进展生存期(PFS)和总生存期(OS)更长。19 Del快速进展的患者可从化疗中获得生存获益,而缓慢进展的患者从化疗或继续使用先前的TKI中均未获得生存获益。然而,在L858R队列中,快速或缓慢进展的患者从继续使用先前的TKI中获益。对于对EGFR-TKI获得性耐药的晚期EGFR阳性NSCLC患者,应根据EGFR-TKI治疗失败模式和EGFR突变亚型进行个体化后续治疗。