Open AccessIDH1/IDH2 Mutations Define the Prognosis and Molecular Profiles of Patients with Gliomas: A Meta-Analysis
Author(s) -
Peng Zou,
Xu Hui,
Pin Chen,
Qing Yan,
Lin Zhao,
Peng Zhao,
Aihua Gu
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0068782
Subject(s) - idh2 , idh1 , isocitrate dehydrogenase , meta analysis , cancer research , biology , mutation , computational biology , genetics , bioinformatics , medicine , enzyme , gene , biochemistry
Background Isocitrate dehydrogenase isoforms 1 and 2 (IDH1 and IDH2 ) mutations have received considerable attention since the discovery of their relation with human gliomas. The predictive value of IDH1 and IDH2 mutations in gliomas remains controversial. Here, we present the results of a meta-analysis of the associations between IDH mutations and both progression-free survival (PFS) and overall survival (OS) in gliomas. The interrelationship between the IDH mutations and MGMT promoter hypermethylation, EGFR amplification, codeletion of chromosomes 1p/19q and TP53 gene mutation were also revealed. Methodology and Principal Findings An electronic literature search of public databases (PubMed, Embase databases) was performed. In total, 10 articles, including 12 studies in English, with 2,190 total cases were included in the meta-analysis. The IDH mutations were frequent in WHO grade II and III glioma (59.5%) and secondary glioblastomas (63.4%) and were less frequent in primary glioblastomas (7.13%). Our study provides evidence that IDH mutations are tightly associated with MGMT promoter hypermethylation ( P <0.001), 1p/19q codeletion ( P <0.001) and TP53 gene mutation ( P <0.001) but are mutually exclusive with EGFR amplification ( P <0.001). This meta-analysis showed that the combined hazard ratio (HR) estimate for overall survival and progression-free survival in patients with IDH mutations was 0.33 (95% CI: 0.25–0.42) and 0.38 (95% CI: 0.21–0.68), compared with glioma patients whose tumours harboured the wild-type IDH . Subgroup analyses based on tumour grade also revealed that the presence of IDH mutations was associated with a better outcome. Conclusion Our study suggests that IDH mutations, which are closely linked to the genomic profile of gliomas, are potential prognostic biomarkers for gliomas.