Quantitative Analysis of the

O(6)-methylguanine-DNA methyltransferase glioblastoma temozolomide

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
27 Jun 2022
Historique:
received: 20 05 2022
revised: 22 06 2022
accepted: 24 06 2022
entrez: 9 7 2022
pubmed: 10 7 2022
medline: 10 7 2022
Statut: epublish

Résumé

Background: Glioblastomas with methylation of the promoter region of the O(6)-methylguanine-DNA methyltransferase (MGMT) gene exhibit increased sensitivity to alkylating chemotherapy. Quantitative assessment of the MGMT promoter methylation status might provide additional prognostic information. The aim of our study was to determine a quantitative methylation threshold for better survival among patients with glioblastomas. Methods: We included consecutive patients ≥18 years treated at our department between 11/2010 and 08/2018 for a glioblastoma, IDH wildtype, undergoing quantitative MGMT promoter methylation analysis. The primary endpoint was overall survival. Results: A total of 321 patients were included. Median overall survival was 12.6 months. Kaplan−Meier and adjusted Cox regression analysis showed better survival for the groups with 16−30%, 31−60%, and 61−100% methylation. In contrast, survival in the group with 1−15% methylation was similar to those with unmethylated promoter regions. A secondary analysis confirmed this threshold. Conclusions: Better survival is observed in patients with glioblastomas with ≥16% methylation of the MGMT promoter region than with <16% methylation. Survival with tumors with 1−15% methylation is similar to with unmethylated tumors. Above 16% methylation, we found no additional benefit with increasing methylation.

Identifiants

pubmed: 35804921
pii: cancers14133149
doi: 10.3390/cancers14133149
pmc: PMC9264886
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : The Department of Neurosurgery, University Hospital Bern, University of Bern
ID : None

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Auteurs

Levin Häni (L)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Monika Kopcic (M)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Mattia Branca (M)

CTU Bern, University of Bern, 3012 Bern, Switzerland.

Alessa Schütz (A)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Michael Murek (M)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Nicole Söll (N)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Erik Vassella (E)

Institute of Pathology, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Andreas Raabe (A)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Ekkehard Hewer (E)

Institute of Pathology, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.
Institute of Pathology, Lausanne University Hospital and University of Lausanne, 1011 Lausanne, Switzerland.

Philippe Schucht (P)

Department of Neurosurgery, Inselspital, Bern University Hospital, University of Bern, 3010 Bern, Switzerland.

Classifications MeSH