ERCC2 polymorphisms and radiation-induced adverse effects on normal tissue: systematic review with meta-analysis and trial sequential analysis

• Published in: Radiation oncology (London, England) Vol. 10; no. 1; p. 247
• Main Authors: Song, Yu-Zhe, Duan, Mei-Na, Zhang, Yu-Yu, Shi, Wei-Yan, Xia, Cheng-Cheng, Dong, Li-Hua
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 01.12.2015; BioMed Central
• Subjects: Analysis; Databases, Factual; Genetic Predisposition to Disease; Genotype; Humans; Medical research; Medicine, Experimental; Odds Ratio; Online databases; Polymorphism, Single Nucleotide - genetics; Radiation; Radiation Injuries - genetics; Xeroderma Pigmentosum Group D Protein - genetics
• ISSN: 1748-717X; 1748-717X
• DOI: 10.1186/s13014-015-0558-6

The relationship between ERCC2 polymorphisms and the risk of radiotoxicity remains inconclusive. The aim of our study is to systematically evaluate the association between ERCC2 polymorphisms and the risk of radiotoxicity. Publications were identified through a search of the PubMed and Web of Science databases up to August 15, 2015. The pooled odds ratios (ORs) with corresponding 95 % confidence intervals (CIs) were calculated to evaluate the association between ERCC2 polymorphisms and radiotoxicity. Trial sequential analysis (TSA) and power calculation were performed to evaluate the type 1 and type 2 errors. Eleven studies involving 2584 patients were ultimately included in this meta-analysis. Conventional meta-analysis identified a significant association between ERCC2 rs13181 polymorphism and radiotoxicity (OR = 0.71, 95 % CI: 0.55-0.93, P = 0.01), but this association failed to get the confirmation of TSA. The minor allele of rs13181 polymorphism may confer a protect effect against radiotoxicity. To confirm this correlation at the level of OR = 0.71, an overall information size of approximate 2800 patients were needed.