Polymorphisms in ERCC1 gene could predict clinical outcome of platinum-based chemotherapy for non-small cell lung cancer patients

被引:20
作者
Zhao, Xin [1 ]
Zhang, Zhiqiang [1 ]
Yuan, Yan [2 ]
Yuan, Xiaomei [1 ]
机构
[1] Xinxiang Med Univ, Dept Respirat, Affiliated Hosp 1, Wei Hui 453100, Peoples R China
[2] Xinxiang Med Univ, Dept Neurol, Affiliated Hosp 1, Wei Hui 453100, Peoples R China
关键词
ERCC1; Polymorphism; NSCLC; Platinum-based chemotherapy; Clinical outcome; NEOADJUVANT CHEMOTHERAPY; TREATMENT RESPONSE; EXPRESSION; SURVIVAL; RISK; ASSOCIATION; STATISTICS;
D O I
10.1007/s13277-014-2033-7
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We analyzed the role of three common single-nucleotide polymorphisms (SNPs) of ERCC1 in predicting the tumor responses and the survival of non-small cell lung cancer (NSCLC) patients who received platinum-based chemotherapy. One hundred ninety-two patients who were identified as stage IV or IIIB/A NSCLC were collected between January 2008 and December 2009. ERCC1 rs11615, rs3212986, and rs2298881 were selected and genotyped by MassARRAYA (R) Analyzer 4 system. One hundred three (53.65 %) patients showed a CR and PR to chemotherapy, and 81 (42.19 %) patients died from NSCLC with the median OS of 35.82 A +/- 15.19 months. Multivariate regression analysis showed that rs11615 TT genotype and T allele were associated with optimal response to chemotherapy, and rs3212986 AA and A allele were correlated with better response to chemotherapy. Cox regression showed that patients carrying the rs11615 TT genotype and T allele and the rs3212986 AA genotype and A allele were significantly associated with higher risk of death from NSCLC. In conclusion, ERCC1 rs11615 and rs3212986 polymorphism were associated with a poor response to chemotherapy and shorter survival time of advanced NSCLC. ERCC1 rs11615 and rs3212986 polymorphisms may be helpful for designing individualized cancer treatment for NSCLC patients.
引用
收藏
页码:8335 / 8341
页数:7
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