Liu Jun-Yan, Zou Ting, Yin Ji-Ye, Wang Zhan, Wang Ying, Liu Zhao-Qian, Chen Juan, Chen Zhi-Wei
Department of Orthopaedics, The First Affiliated Hospital of the University of South China, Hengyang 421001, China.
National Institution of Drug Clinical Trial, Xiangya Hospital, Central South University, Changsha, Hunan, P.R.China.
J Cancer. 2020 Jul 9;11(18):5281-5288. doi: 10.7150/jca.46150. eCollection 2020.
To investigate the relationships between genetic variants in DNA mismatch repair pathway genes and the prognosis of platinum-based chemotherapy in lung cancer patients. 346 lung cancer patients who received at least two cycles of platinum-based chemotherapy were recruited in this study. A total of 35 single nucleotide polymorphisms in 7 DNA mismatch repair genes were genotyped to investigate their associations with platinum-based chemotherapy prognosis. The results revealed that patients carried rs4608577 TT genotype had a significantly shorter progression free survival than patients with GG or GT genotypes (Additive model: =0.003, OR =0.94, 95% CI =0.33-1.57). Patients with rs707937 TT genotype had a significantly longer overall survival than patients with GG or GT genotypes (Additive model: =0.0003, OR=0.75, 95% CI =0.35-1.14). Eight SNPs and fourteen SNPs were related to progression free survival and overall survival in subgroup analyses, respectively. : Our findings suggest that the rs4608577 and rs707937 may be potential clinical biomarkers for predicting platinum-based chemotherapy prognosis in lung cancer patients.
为了研究DNA错配修复通路基因中的遗传变异与肺癌患者铂类化疗预后之间的关系。本研究招募了346例接受至少两个周期铂类化疗的肺癌患者。对7个DNA错配修复基因中的35个单核苷酸多态性进行基因分型,以研究它们与铂类化疗预后的关联。结果显示,携带rs4608577 TT基因型的患者无进展生存期明显短于携带GG或GT基因型的患者(加性模型:=0.003,OR =0.94,95%CI =0.33 - 1.57)。携带rs707937 TT基因型的患者总生存期明显长于携带GG或GT基因型的患者(加性模型:=0.0003,OR =0.75,95%CI =0.35 - 1.14)。在亚组分析中,分别有8个单核苷酸多态性和14个单核苷酸多态性与无进展生存期和总生存期相关。我们的研究结果表明,rs4608577和rs707937可能是预测肺癌患者铂类化疗预后的潜在临床生物标志物。