RRM1 expression and clinical outcome of gemcitabine-containing chemotherapy for advanced non-small-cell lung cancer: A meta-analysis

被引:65
作者
Gong, Weiyi [1 ]
Zhang, Xinmin [1 ]
Wu, Jinfeng [1 ]
Chen, Lili [2 ]
Li, Lulu [1 ]
Sun, Jing [1 ]
Lv, Yubao [1 ]
Wei, Xiaobai [1 ]
Du, Yijie [1 ]
Jin, Hualiang [1 ]
Dong, Jingcheng [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Integrated Tradit Chinese & Western Med, Shanghai 200433, Peoples R China
[2] Fudan Univ, Huashan Hosp, Dept Endocrinol & Metab, Shanghai 200433, Peoples R China
关键词
RRM1; Gemcitabine; NSCLC; Meta-analysis; Median survival; Time to progression; MESSENGER-RNA EXPRESSION; RIBONUCLEOTIDE REDUCTASE; INDIVIDUALIZED THERAPY; SHORTER SURVIVAL; EFFICACY; RESISTANCE; M1; DOCETAXEL; NSCLC; ERCC1;
D O I
10.1016/j.lungcan.2011.08.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The predictive value of RRM1 to therapeutic efficacy of gemicitabine-containing chemotherapy in patients with advanced non-small-cell lung cancer (NSCLC) remains disputable. This meta-analysis is performed to systematically evaluate whether RRM1 expression is associated with the clinical outcome of gemcitabine-containing regimen in advanced NSCLC. Methods: An electronic search was conducted using the databases Pubmed, Medline, EMBASE, Cochrane library and CNKI, from inception to May, 2011. A systemic review of the studies on the association between RRM1 expression in advanced NSCLC and clinical outcome of gemcitabine-containing regimen was performed. Pooled odds ratios (OR) for the response rate, weighted median survival and time to progression were calculated using the software Revman 5.0. Results: The search strategy identified 18 eligible studies (n = 1243). Response rate to gemcitabine-containing regimen was significantly higher in patients with low/negative RRM1 (OR = 0.31, 95% CI 0.21-0.45, P<0.00001). NSCLC patients with low/negative RRM1 who were treated with gemicitabine-containing regimen survived 3.94 months longer (95% CI 2.15-5.73, P<0.0001) and had longer time to Progression for 2.64 months (95% CI 0.39-4.89, P = 0.02) than those with high/positive RRM1. Conclusions: Low/negative RRM1 expression in advanced NSCLC was associated with higher response rate to gemcitabine-containing regimen and better prognosis. Large phase III randomized trials are required to identify whether RRM1 detection is clinically valuable for predicting the prognosis and sensitivity to gemcitabine-containing regimen in advanced NSCLC. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:374 / 380
页数:7
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