Department of Molecular Biology .
Biomarkers. 2014 Mar;19(2):128-34. doi: 10.3109/1354750X.2014.882414. Epub 2014 Feb 5.
In the present study, we performed this meta-analysis to estimate the association between excision repair cross-complementation group 1 (ERCC1) gene polymorphism and clinical resistance to platinum-based chemotherapy in the patients with epithelial ovarian cancer (EOC).
A total of 10 studies consist of 1479 EOC patients relating ERCC1 rs11615C/T and rs3212986C/A polymorphisms to the response of platinum-based chemotherapy were included in this meta-analysis.
The analysis showed that the AA genotype of the rs3212986C/A polymorphism in ERCC1 was associated with progression-free survival of EOC patients (HR = 1.39, 95% CI = 1.12-1.73) and that the CA or AA genotypes could influence overall survival (HR = 1.28, 95% CI = 1.05-1.56; and HR = 1.55, 95% CI = 1.17∼2.05, respectively).
The ERCC1 rs3212986C/A polymorphism may be a useful prognostic marker in platinum-based treatment of EOC.
在本研究中,我们进行了这项荟萃分析,以评估切除修复交叉互补组 1(ERCC1)基因多态性与上皮性卵巢癌(EOC)患者对铂类化疗的临床耐药性之间的关系。
共有 10 项研究纳入了 1479 名 EOC 患者,这些研究涉及 ERCC1 rs11615C/T 和 rs3212986C/A 多态性与铂类化疗反应的关系。
分析表明,ERCC1 中 rs3212986C/A 多态性的 AA 基因型与 EOC 患者的无进展生存期相关(HR=1.39,95%CI=1.12-1.73),CA 或 AA 基因型可能影响总生存期(HR=1.28,95%CI=1.05-1.56;和 HR=1.55,95%CI=1.17-2.05)。
ERCC1 rs3212986C/A 多态性可能是 EOC 铂类治疗中有用的预后标志物。