Cancer Genomics & Proteomics · 2018 · 56 citations · 40 references
MedicineMolecular MedicineOncologyCancer GeneticsMolecular OncologyNeuro-oncologyBrain TumorsCancer BiomarkersCancer Survival AnalysisDna Methylation ProfilingGlioblastomaNext-generation Sequencing In OncologyGlioblastoma BiomarkersGlioblastoma ChemotherapyGlioblastoma EpigeneticsGlioblastoma PrognosisHigh-resolution Melting AnalysisPrognostic PredictionPromoter MethylationTemozolomide Therapy
BACKGROUND: -methylguanine-DNA methyltransferase (MGMT) gene promoter predicts response to temozolomide in patients with glioblastoma, no consensus exists as to which assay is best for its detection. MATERIALS AND METHODS: Methylation of MGMT promoter was examined by methylation-specific polymerase chain reaction (MSP), quantitative real-time MSP, methylation-sensitive high-resolution melting analysis, and two commercial pyrosequencing (PSQ) kits. Survival was compared among 48 patients with glioblastoma according to assay results. RESULTS: Only PSQ and MSP significantly separated patients who benefited from temozolomide, with PSQ being the superior method. For PSQ analysis, the cut-off value that best correlated with prognostic outcome was 7% methylation of MGMT. Median survival in patients with MGMT promoter methylation above this cut-off value was 7.8 months longer compared to those with less than 7% methylation. Two-year overall survival for the two groups was 42% and 7.4%, respectively. CONCLUSION: PSQ is the method of choice for MGMT promoter methylation analysis in routine clinical practice.
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Radiotherapy plus Concomitant and Adjuvant Temozolomide for Glioblastoma
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<i>MGMT</i> Gene Silencing and Benefit from Temozolomide in Glioblastoma
Monika E. Hegi, Annie‐Claire Diserens, Thierry Gorlia et al. · New England Journal of Medicine · 2005 · 7.3K citations · Full text