Antiseizure medication in patients with Glioblastoma- a collaborative cohort study.


Journal

Seizure
ISSN: 1532-2688
Titre abrégé: Seizure
Pays: England
ID NLM: 9306979

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 25 08 2020
revised: 12 03 2021
accepted: 13 03 2021
pubmed: 25 3 2021
medline: 13 7 2021
entrez: 24 3 2021
Statut: ppublish

Résumé

We investigated, whether epileptic seizures (ES) as presenting symptom in adult patients with GBM are associated with better Overall Survival (OS) compared to ES presenting later during the course of GBM, and efficacy and safety of different antiseizure medications (ASMs). Retrospective consecutive cohort study of adults with GBM: 50 from Norway and 50 from Italy. We compared the time to changing ASM treatments. OS was investigated with a Cox regression model adjusted for time dependency. Median follow-up was 17 months from GBM diagnosis. ES were the presenting symptom in 49 patients. All patients received ASM treatment. LEV was the first ASM in the majority of patients and the most effective at one year from the first prescription, (p = 0.004). Occurrence of adverse events (AEs) was similar between LEV and other ASMs (p = 0.47). Poorer OS correlated with older age at GBM diagnosis, country and ASM therapy. A negative impact of ASMs on OS was observed for LEV in a univariate and multivariate analysis, and for VPA (only in multivariate analysis), even when adjusted for O6-methylguanine-DNA-methyltransferase (MGMT) methylation status. Patients with ES as the onset symptom of GBM and patients who had first ES later had similar OS (p = 0.87). ES as the GBM debut symptom did not lead to a longer OS. LEV was a more effective ASM compared to other treatments with no differences regarding AEs between LEV and other ASMs. Surprisingly, in our patients LEV and VPA were associated with worse OS than other ASMs. This result should be interpreted with caution due to the retrospective nature of this study along with the many variables which may affect the outcome in this population.

Identifiants

pubmed: 33761391
pii: S1059-1311(21)00088-1
doi: 10.1016/j.seizure.2021.03.012
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107-113

Informations de copyright

Copyright © 2021. Published by Elsevier Ltd.

Auteurs

Kristin M Knudsen-Baas (KM)

Department of Clinical Medicine, University of Bergen, Bergen, Norway; The National Center for Epilepsy, Norway. Electronic address: kriskn@ous-hf.no.

Anette M Storstein (AM)

Department of Neurology, Haukeland University Hospital, Bergen, Norway. Electronic address: anette.margrethe.storstein@helse-bergen.no.

Alessia Zarabla (A)

Center for Tumor-related Epilepsy, UOSD Neuroncology, Regina Elena National Cancer Institute IRCCS, Rome, Italy. Electronic address: alessiazarabla@libero.it.

Andrea Maialetti (A)

Center for Tumor-related Epilepsy, UOSD Neuroncology, Regina Elena National Cancer Institute IRCCS, Rome, Italy. Electronic address: andrea.maialetti@libero.it.

Diana Giannarelli (D)

Biostatistic Unit, Regina Elena National Cancer Institute IRCCS, Rome, Italy. Electronic address: diana.giannarelli@ifo.gov.it.

Ettore Beghi (E)

Laboratorio Malattie Neurologiche, IRCCS - Istituto "Mario Negri", Milano, Italy. Electronic address: ettore.beghi@marionegri.it.

Marta Maschio (M)

Center for Tumor-related Epilepsy, UOSD Neuroncology, Regina Elena National Cancer Institute IRCCS, Rome, Italy. Electronic address: Marta.maschio@ifo.gov.it.

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