Hu Xue-Ying, Huang Xiang-Yang, Ma Jie, Zuo Yang, Luo Ning-Bin, Lai Shao-Lv, Su Dan-Ke
Department of Radiology, Affiliated Oncology Hospital of Guangxi Medical University, 71 Hedi Road, Nanning, 530021, Guangxi, People's Republic of China.
Tumour Biol. 2016 Jan;37(1):151-62. doi: 10.1007/s13277-015-4401-3. Epub 2015 Nov 14.
Observational studies have reported controversial results on the association between GSTT1 and GSTM1 genotypes and treatment outcome of breast cancer. The purpose of this study is to evaluate the association between GSTT1 and GSTM1 and treatment outcome in breast cancer patients. Eligible studies were searched in PubMed, EMBASE, Cochrane Library, and China National Knowledge Infrastructure databases. A random-effect model or fixed-effect model was used to calculate the overall combined risk estimates. Twenty-one studies with a total of 4990 patients were included in this meta-analysis. The GSTM1 null genotype (odds ratio (OR) = 1.33, 95 % confidence interval (CI) 1.01-1.75, P = 0.046) and GSTT1/GSTM1 double null genotype (OR = 2.22, 95 % CI 1.02-4.84, P = 0.045) were significantly associated with an increased tumor response. A reduced overall survival (hazard ratio (HR) = 0.84, 95 % CI 0.72-0.98, P = 0.024) was observed in GSTM1 null genotype, especially in mixed descent (HR = 0.77, 95 % CI 0.61-0.96, P = 0.018) and large sample size (HR = 0.85, 95 % CI 0.72-0.99, P = 0.033). Evidence of publication bias was observed in GSTM1 genotype rather than in GSTT1 genotype. This meta-analysis suggests that GSTM1 null and GSTT1/GSTM1 double null polymorphisms might be significantly associated with an increased tumor response. However, the GSTM1 null genotype might be significantly associated with a reduced overall survival. Future studies are warranted to confirm these findings.
观察性研究报告了谷胱甘肽硫转移酶T1(GSTT1)和谷胱甘肽硫转移酶M1(GSTM1)基因多态性与乳腺癌治疗结果之间关联的矛盾结果。本研究的目的是评估GSTT1和GSTM1与乳腺癌患者治疗结果之间的关联。在PubMed、EMBASE、Cochrane图书馆和中国知网数据库中检索符合条件的研究。采用随机效应模型或固定效应模型计算总体合并风险估计值。本荟萃分析纳入了21项研究,共4990例患者。GSTM1无效基因型(比值比(OR)=1.33,95%置信区间(CI)1.01 - 1.75,P = 0.046)和GSTT1/GSTM1双无效基因型(OR = 2.22,95% CI 1.02 - 4.84,P = 0.045)与肿瘤反应增加显著相关。在GSTM1无效基因型中观察到总生存期缩短(风险比(HR)= 0.84,95% CI 0.72 - 0.98,P = 0.024),尤其是在混合血统(HR = 0.77,95% CI 0.61 - 0.96,P = 0.018)和大样本量(HR = 0.85,95% CI 0.72 - 0.99,P = 0.033)的患者中。在GSTM1基因型而非GSTT1基因型中观察到发表偏倚的证据。本荟萃分析表明,GSTM1无效和GSTT1/GSTM1双无效多态性可能与肿瘤反应增加显著相关。然而,GSTM1无效基因型可能与总生存期缩短显著相关。有必要进行进一步研究以证实这些发现。