Evidence map›Paper›PMID 42397117›Full record

ArticleEpilepsia open2026

Real-world use of Cenobamate in pediatric drug-resistant epilepsy: A European multicenter retrospective study.

Konstantin L Makridis, Thomas Bast, Stéphane Auvin, Pavel Krsek, Matyas Ebel, Eva Breuer, Mira Beckhaus, Matúš Bašovský, Pavlína Danhofer, Ondřej Horák and 5 more

Abstract read
In one paragraph

Article in Epilepsia open, 2026. 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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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Konstantin L MakridisDepartment of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0002-2609-4557
Thomas BastEpilepsy Center Kork, Kehl, Germany.
Stéphane AuvinAP-HP, Pediatric Neurology Department, Reference Center for Rare Epilepsies, Member of ERN Epicare, Hôpital Universitaire Robert Debré, Paris, France.ORCID https://orcid.org/0000-0003-3874-9749
Pavel KrsekDepartment of Paediatric Neurology, Motol Epilepsy Center, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Full Member of the ERN EpiCARE and Epilepsy Research Centre Prague - EpiReC Consortium, Prague, Czech Republic.
Matyas EbelDepartment of Paediatric Neurology, Motol Epilepsy Center, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Full Member of the ERN EpiCARE and Epilepsy Research Centre Prague - EpiReC Consortium, Prague, Czech Republic.
Eva BreuerEpilepsy-Center Berlin-Brandenburg, Ev. Krankenhaus Königin Elisabeth Herzberge, Berlin, Germany.
Mira BeckhausEpilepsy-Center Berlin-Brandenburg, Ev. Krankenhaus Königin Elisabeth Herzberge, Berlin, Germany.
Matúš BašovskýDepartment of Child Neurology, Thomayer University Hospital, Prague, Czech Republic.
Pavlína DanhoferDepartment of Paediatric Neurology, Faculty of Medicineof Masaryk University and University Hospital Brno, Brno Epilepsy Center, EpiCARE, Brno, Czech Republic.
Ondřej HorákDepartment of Paediatric Neurology, Faculty of Medicineof Masaryk University and University Hospital Brno, Brno Epilepsy Center, EpiCARE, Brno, Czech Republic.
Alessandro OrsiniPediatric Neurology, University Hospital of Pisa, Azienda Ospedaliero Universitaria Pisana, Pisa, Italy.
Gonzalo Alonso Ramos RiveraDepartment of Neurology, Bory Hospital, Bratislava, Slovakia.ORCID https://orcid.org/0009-0003-4184-0321
Hana MedřickáDepartment of Paediatric Neurology, University Hospital Ostrava, Ostrava, Czech Republic.
Steffen SyrbeDivision of Pediatric Epileptology, Center for Pediatric and Adolescent Medicine, Clinic 1, Medical Faculty of Heidelberg, Heidelberg University, Heidelberg, Germany.
Angela M KaindlDepartment of Pediatric Neurology, Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID https://orcid.org/0000-0001-9454-206X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pediatric drug-resistant epilepsy (DRE) remains a significant clinical challenge, with few effective pharmacological options. This European multicenter retrospective study assessed the real-world efficacy, tolerability, and retention of off-label cenobamate (CNB) in 108 children and adolescents with DRE (median age: 13.83 years, range 3.9-19.8). Overall, 57/108 patients (52.8%) achieved a ≥50% seizure reduction, including 20/108 (18.5%) who were seizure-free during the documented interval between visits. The median monthly seizure frequency declined from 30 to 9. Median follow-up was 581.5 days (IQR 340,8; range 27-1160); 5 patients had follow-up ≤90 days and 10 had follow-up <180 days. In sensitivity analyses excluding patients with follow-up ≤90 days and <180 days, ≥50% responder rates were 54.4% and 56.1%, respectively. Concomitant ASM dose reductions and discontinuations occurred in 44% and 51% of patients, respectively, with the median ASM count declining from 3 to 2. Adverse events were documented in 57.4%, most frequently fatigue, vertigo, and behavioral symptoms. No cases of DRESS were reported. CNB retention at 12 months was 86.8% and was higher in patients without adverse events (93.5% vs. 81.6%, p = 0.0076). The initiation dose was most commonly 12.5 mg (0.25 mg/kg/day, IQR 0.12), with titration to a median maintenance dose of 3.57 mg/kg/day (IQR 1.95; range 0.3-10). These findings suggest that CNB is a generally well-tolerated and clinically effective adjunctive treatment in pediatric DRE, with the potential to reduce polypharmacy and support long-term adherence. Controlled prospective studies are needed to confirm these results and to establish safe, evidence-based use of CNB in children. PLAIN LANGUAGE SUMMARY: Many children and adolescents with drug-resistant epilepsy do not respond to available medications. In this European multicenter study, we evaluated cenobamate, used off label, in 108 young patients with severe epilepsy. More than half had their seizures reduced by at least 50%, and nearly one in five became seizure-free. Seizure frequency dropped markedly, and many patients could reduce other anti-seizure medications. Side effects were common but usually mild, and most patients continued treatment long term. These results suggest cenobamate may be a useful option in pediatric drug-resistant epilepsy, but prospective studies are needed to confirm safety and effectiveness.

Indexed as

anti‐seizure medicationcenobamatedrug‐resistant epilepsyepilepsypediatric

Identifiers

PMID42397117
PMCPMC13394996

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