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Impact of timing of antiseizure medication withdrawal on seizure recurrence in glioma patients: a retrospective observational study.
van der Meer, Pim B; Dirven, Linda; Fiocco, Marta; Vos, Maaike J; Kerkhof, Melissa; Kouwenhoven, Mathilde C M; van den Bent, Martin J; Taphoorn, Martin J B; Koekkoek, Johan A F.
Afiliación
  • van der Meer PB; Department of Neurology, Leiden University Medical Center, PO BOX 9600, 2300 RC, Leiden, The Netherlands. pbvandermeer@lumc.nl.
  • Dirven L; Department of Neurology, Leiden University Medical Center, PO BOX 9600, 2300 RC, Leiden, The Netherlands.
  • Fiocco M; Department of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
  • Vos MJ; Department of Biomedical Data Sciences, Medical Statistics, Leiden University Medical Center, Leiden, The Netherlands.
  • Kerkhof M; Mathematical Institute, Leiden University, Leiden, The Netherlands.
  • Kouwenhoven MCM; Department of Neurology, Leiden University Medical Center, PO BOX 9600, 2300 RC, Leiden, The Netherlands.
  • van den Bent MJ; Department of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
  • Taphoorn MJB; Department of Neurology, Haaglanden Medical Center, The Hague, The Netherlands.
  • Koekkoek JAF; Department of Neurology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
J Neurooncol ; 164(3): 545-555, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37755633
ABSTRACT

BACKGROUND:

Withdrawal of antiseizure medication treatment (ASM) can be considered after completion of antitumour treatment in glioma patients who no longer suffer from seizures. We compared the risk for recurrent seizures after ASM withdrawal between patients with short-term, medium-term versus long-term seizure freedom after antitumour treatment.

METHODS:

In this retrospective observational study, the primary outcome was time to recurrent seizure, from the starting date of no ASM treatment up to 36 months follow-up. Cox proportional hazards models were used to study the effect of risk factors on time to recurrent seizure. Stratification was done with information known at baseline. Short-term seizure freedom was defined as ≥ 3 months, but < 12 months; medium-term as 12-24 months; and long-term as ≥ 24 months seizure freedom from the date of last antitumour treatment.

RESULTS:

This study comprised of 109 patients; 31% (34/109) were in the short-term, 29% (32/109) in the medium-term, and 39% (43/109) in the long-term group. A recurrent seizure was experienced by 47% (16/34) of the patients in the short-term, 31% (10/32) in the medium-term, and 44% (19/43) in the long-term group. Seizure recurrence risk was similar between patients in the short-term group as compared to the medium-term (cause-specific adjusted hazard ratio [aHR] = 0.65 [95%CI = 0.29-1.46]) and long-term group (cause-specific aHR = 1.04 [95%CI = 0.52-2.09]).

CONCLUSIONS:

Seizure recurrence risk is relatively similar between patients with short-term, medium-term, and long-term seizure freedom after completion of antitumour treatment.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Epilepsia Generalizada / Glioma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurooncol Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Epilepsia Generalizada / Glioma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: J Neurooncol Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos