Favorable role of IDH1/2 mutations aided with MGMT promoter gene methylation in the outcome of patients with malignant glioma

AIMThe implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter methylation were evaluated for prognostic outcome of glioma patients. MATERIALS & METHODSGlioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation by DNA sequencing and methylation-specific PC...

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Veröffentlicht in:Future science OA 2021-03, Vol.7 (3), p.FSO663-FSO663
Hauptverfasser: Pandith, Arshad A, Qasim, Iqbal, Baba, Shahid M, Koul, Aabid, Zahoor, Wani, Afroze, Dil, Lateef, Adil, Manzoor, Usma, Bhat, Ina A, Sanadhya, Dheera, Bhat, Abdul R, Ramzan, Altaf U, Mohammad, Fozia, Anwar, Iqra
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Sprache:eng
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Zusammenfassung:AIMThe implications of molecular biomarkers IDH1/2 mutations and MGMT gene promoter methylation were evaluated for prognostic outcome of glioma patients. MATERIALS & METHODSGlioma cases were analyzed for IDH1/2 mutations and MGMT promoter methylation by DNA sequencing and methylation-specific PCR, respectively. RESULTSMutations found in IDH1/2 genes totaled 63.4% (N = 40) wherein IDH1 mutations were significantly associated with oligidendrioglioma (p = 0.005) and astrocytoma (p = 0.0002). IDH1 mutants presented more, 60.5% in MGMT promoter-methylated cases (p = 0.03). IDH1 mutant cases had better survival for glioblastoma and oligodendrioglioma (log-rank p = 0.01). Multivariate analysis confirmed better survival in MGMT methylation carriers (hazard ratio [HR]: 0.59; p = 0.031). Combination of both biomarkers showed better prognosis on temozolomide (p < 0.05). CONCLUSIONIDH1/2 mutations proved independent prognostic factors in glioma and associated with MGMT methylation for better survival.
ISSN:2056-5623
2056-5623
DOI:10.2144/fsoa-2020-0057