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Association of TERT Polymorphisms with Clinical Outcome of Non-Small Cell Lung Cancer Patients

Authors :
Wenting Wu
Hui Li
Chunxue Bai
Qiang Li
Jiucun Wang
Daru Lu
Shiming Wang
Xueying Zhao
Xun Wang
Wenbin Liu
Junjie Wu
Ji Qian
Ke Ma
Xiaoying Li
Haijian Wang
Zhiqiang Gao
Baohui Han
Source :
PLoS ONE, Vol 10, Iss 5, p e0129232 (2015), PLoS ONE
Publication Year :
2015
Publisher :
Public Library of Science (PLoS), 2015.

Abstract

TERT is of great importance in cancer initiation and progression. Many studies have demonstrated the TERT polymorphisms as risk factors for many cancer types, including lung cancer. However, the impacts of TERT variants on cancer progression and treatment efficacy have remained controversial. This study aimed to investigate the association of TERT polymorphisms with clinical outcome of advanced non-small cell lung cancer (NSCLC) patients receiving first-line platinum-based chemotherapy, including response rate, clinical benefit, progression-free survival (PFS), overall survival (OS), and grade 3 or 4 toxicity. Seven polymorphisms of TERT were assessed, and a total of 1004 inoperable advanced NSCLC patients treated with platinum-based chemotherapy were enrolled. It is exhibited that the variant heterozygote of rs4975605 showed significant association with a low rate of clinical benefit, and displayed a much stronger effect in never-smoking female subset, leading to the clinical benefit rate decreased from 82.9% (C/C genotype) to 56.4% (C/A genotype; adjusted OR, 3.58; P=1.40×10(-4)). It is also observed that the polymorphism rs2736109 showed significant correlation with PFS (log-rank P=0.023). In age > 58 subgroup, patients carrying the heterozygous genotype had a longer median PFS than those carrying the wild-type genotypes (P=0.002). The results from the current study, for the first time to our knowledge, provide suggestive evidence of an effect of TERT polymorphisms on disease progression variability among Chinese patients with platinum-treated advanced NSCLC.

Details

ISSN :
19326203
Volume :
10
Database :
OpenAIRE
Journal :
PLOS ONE
Accession number :
edsair.doi.dedup.....91b4e76fe174bf3e91bec011906672de