Evidence map›Paper›PMID 41258589›Full record

ArticleJournal of neuro-oncology2025

Seizure characteristics in epilepsy patients with a primary brain tumor.

Lena Vegh, Felix Benninger, Idit Tamir

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Article in Journal of neuro-oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Lena VeghGray Faculty of Medical & Health Sciences, Tel Aviv University, Tel Aviv, Israel. lena.a.vegh@gmail.com.ORCID http://orcid.org/0009-0004-4888-2054
Felix BenningerDepartment of Neurology, Rabin Medical Center, Petah-Tikva, Israel.ORCID http://orcid.org/0000-0003-3097-4693
Idit TamirDepartment of Neurosurgery, Rabin Medical Center, Petah-Tikva, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEpilepsy is among the most prevalent neurological disorders, with one in 10 people experiencing a seizure in their lifetime. In adults, brain tumors are a common cause. While tumor-control outcomes are well studied, less is known about seizure control in this population.

methodsWe retrospectively reviewed the Clalit Dan–Petah Tikva County database (2000–2019), covering 1.55 million patients. Adults with primary brain tumors and epilepsy were identified by ICD-10 codes. Seizure control and management were assessed through anti-seizure medication (ASM) prescriptions, follow-up care, hospitalizations, and evaluation by specialized epilepsy clinics.

resultsAmong 1,557,764 individuals, 17,225 (1.1%) adults were diagnosed with a brain tumor, of whom 14.7% (n = 2,532) had secondary epilepsy. Glioma patients had more than double the epilepsy rate (29.2%, n = 878) compared to meningioma (13.1%, n = 1,417). Most epilepsy cases were associated with benign tumors (65.6%, n = 1,661). Overall, 9.7% (n = 1,672) were classified as high-risk for drug-resistant epilepsy (DRE), yet only 0.5% (n = 89) had a formal diagnosis. Of these, just 12 (0.7%) received follow-up at a specialized epilepsy clinic; the remainder were managed by community neurologists, oncologists, neurosurgeons, or primary care physicians. None of the patients with intractable epilepsy underwent evaluation for epilepsy surgery.

conclusionDespite adequate tumor control, many patients with tumor-related epilepsy continue to experience seizures after resection and oncological treatment, due to suboptimal management or intractability. Under-recognition of DRE and low referral rates to specialized epilepsy centers highlight a significant treatment gap. Improved referral pathways and comprehensive evaluations are needed to optimize seizure outcomes in this population.

Indexed as

Brain NeoplasmsEpilepsySeizuresAdolescentAdultAgedAnticonvulsantsFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective StudiesYoung AdultAnticonvulsantsAnti-seizure medicationDrug-resistant epilepsyEpilepsyGliomaMeningioma

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.