Wang Cong, Chen Fang, Liu Yichen, Xu Qingqing, Guo Liang, Zhang Xiaoqing, Ruan Yunfeng, Shi Ye, Shen Lu, Li Mo, Du Huihui, Sun Xiaofang, Ma Jingsong, He Lin, Qin Shengying
Life Science College, Anhui Medical University, Hefei, China.
Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders (Ministry of Education), Shanghai Jiao Tong University, Shanghai, China.
Front Pharmacol. 2018 Apr 11;9:360. doi: 10.3389/fphar.2018.00360. eCollection 2018.
The efficacy of erlotinib treatment for advanced non-small cell lung cancer (NSCLC) is due to its action as an epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI). Patients treated with erlotinib experience different drug responses. The effect of germline mutations on therapeutic responses and adverse drug responses (ADRs) to erlotinib in Chinese patients requires elucidation. Sixty Han Chinese advanced non-small cell lung cancer patients received erlotinib monotherapy and, for each participant, 76 candidate genes (related to EGFR signaling, drug metabolism and drug transport pathways) were sequenced and analyzed. The single-nucleotide polymorphisms (SNPs) rs1042640 in , rs1060463, and rs1064796 in , and rs2074900 in were significantly associated with therapeutic responses to erlotinib. Rs1064796 in and rs10045685 in were significantly associated with adverse drug reaction. Moreover, analysis of a validation cohort confirmed the significant association between rs10045685 in and erlotinib adverse drug response(unadjusted = 0.015). This study provides comprehensive, systematic analyses of genetic variants associated with responses to erlotinib in Chinese advanced non-small cell lung cancer patients. Newly-identified SNPs may serve as promising markers to predict responses and safety in erlotinib-treated advanced non-small cell lung cancer patients after chemotherapy doublet.
厄洛替尼治疗晚期非小细胞肺癌(NSCLC)的疗效归因于其作为表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)的作用。接受厄洛替尼治疗的患者会有不同的药物反应。在中国患者中,种系突变对厄洛替尼治疗反应及药物不良反应(ADR)的影响有待阐明。60例汉族晚期非小细胞肺癌患者接受了厄洛替尼单药治疗,对每位参与者的76个候选基因(与EGFR信号传导、药物代谢及药物转运途径相关)进行了测序和分析。 中的单核苷酸多态性(SNP)rs1042640、 中的rs1060463和rs1064796以及 中的rs2074900与厄洛替尼的治疗反应显著相关。 中的rs1064796和 中的rs10045685与药物不良反应显著相关。此外,对一个验证队列的分析证实了 中的rs10045685与厄洛替尼药物不良反应之间的显著关联(未校正 = 0.015)。本研究对中国晚期非小细胞肺癌患者中与厄洛替尼反应相关的基因变异进行了全面、系统的分析。新发现的SNP可能成为预测接受厄洛替尼治疗的晚期非小细胞肺癌患者在双药化疗后反应和安全性的有前景的标志物。