Evidence map›Paper›PMID 42625556›Full record

ArticleEpilepsia open2026

DECREASE study: A European pool-analysis of patients with significant reductions in concomitant antiseizure medications in cenobamate Early Access Programs.

Vicente Villanueva, Simona Lattanzi, Javier Peña-Ceballos, Rhys H Thomas, Juan Rodríguez-Uranga, Zsófia Jordán, Bernhard J Steinhoff, Randi von Wrede, Norman Delanty, Patrick B Moloney and 16 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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

26 authors.

Vicente VillanuevaDepartment of Neurology, Refractory Epilepsy Unit, Hospital Universitario y Politécnico La Fe, Member of ERN EpiCARE, Valencia, Spain.ORCID https://orcid.org/0000-0003-2080-8042
Simona LattanziNeurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.ORCID https://orcid.org/0000-0001-8748-0083
Javier Peña-CeballosDepartment of Neurology, Beaumont Hospital, Dublin, Ireland.ORCID https://orcid.org/0000-0001-7260-1292
Rhys H ThomasDepartment of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UK.ORCID https://orcid.org/0000-0003-2062-8623
Juan Rodríguez-UrangaCentro Neurología Avanzada, Sevilla, Spain.ORCID https://orcid.org/0009-0007-5354-1256
Zsófia JordánEpilepsy Unit, Department of Neurology, Semmelweis University Clinic for Neurosurgery and Neurointervention, Budapest, Hungary.ORCID https://orcid.org/0000-0002-6195-9130
Bernhard J SteinhoffDepartment for Adults, Kork Epilepsy Centre, Kehl-Kork, Germany.ORCID https://orcid.org/0000-0001-5995-5862
Randi von WredeDepartment of Epileptology, University Hospital Bonn, Bonn, Germany.ORCID https://orcid.org/0000-0002-9430-5037
Norman DelantyDepartment of Neurology, Beaumont Hospital, Dublin, Ireland.ORCID https://orcid.org/0000-0002-3953-9842
Patrick B MoloneyDepartment of Neurology, Beaumont Hospital, Dublin, Ireland.ORCID https://orcid.org/0000-0003-0997-2087
Roberta RobertiCRUISE Research Center, Science of Health Department, Magna Græcia University, Catanzaro, Italy.
Giovanni BoeroComplex Structure of Neurology, SS Annunziata Hospital, Taranto, Italy.
Laura CanafogliaEpilepsy Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy.ORCID https://orcid.org/0000-0002-5385-761X
Nicola SpecchioNeurology, Epilepsy and Movement Disorders Unit, Bambino Gesù Children's Hospital, IRCCS, Full Member of ERN EpiCARE, Rome, Italy.ORCID https://orcid.org/0000-0002-8120-0287
Antonio GambardellaDepartment of Neurology, Policlinico Universitario, Azienda Ospedaliero-Universitaria "Renato Dulbecco", Catanzaro, Italy.ORCID https://orcid.org/0000-0001-7384-3074
Edoardo FerlazzoDepartment of Medical and Surgical Sciences, Magna Graecia University of Catanzaro, Catanzaro, Italy.
Francesca Felicia OpertoCRUISE Research Center, Science of Health Department, Magna Græcia University, Catanzaro, Italy.ORCID https://orcid.org/0000-0002-2444-8761
Elena TartaraIRCCS Mondino Foundation, Epilepsy Center, Full Member of ERN EpiCARE, Pavia, Italy.ORCID https://orcid.org/0000-0003-1656-5420
Hester GarrattDepartment of Neurology, Royal Victoria Infirmary, Newcastle upon Tyne, UK.
Dániel FabóDepartment of Neurology, University of Szeged, Szeged, Hungary.ORCID https://orcid.org/0000-0001-5141-5351
Asier Gómez-IbáñezDepartment of Neurology, Clínica Universidad de Navarra, Madrid, Spain.
Gustavo Torres-GaonaDepartment of Neurology, Clínica Corachan, Barcelona, Spain.
Yulia NovitskayaDepartment of Neurosurgery, Epilepsy Center, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Member of ERN EpiCARE, Freiburg, Germany.ORCID https://orcid.org/0000-0002-0905-9936
Rainer SurgesClinic for Neurology and Neurophysiology, University of Freiburg, Freiburg, Germany.ORCID https://orcid.org/0000-0002-3177-8582
Kevin HampelDepartment of Neurology, Refractory Epilepsy Unit, Hospital Universitario y Politécnico La Fe, Member of ERN EpiCARE, Valencia, Spain.ORCID https://orcid.org/0000-0003-3582-060X
Andreas Schulze-BonhageDepartment of Neurosurgery, Epilepsy Center, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Member of ERN EpiCARE, Freiburg, Germany.ORCID https://orcid.org/0000-0003-2382-0506

Funding

Angelini Pharma
6 · The paper itself

Abstract

objectiveTo evaluate the effectiveness and tolerability of cenobamate in patients with a significant reduction in concomitant antiseizure medication (ASM) in European cenobamate Early Access Programs (EAPs).

methodAnonymized patient data from real-world studies/registries associated with European cenobamate EAPs were pooled. Patients were included if they had significantly reduced their concomitant drug load (i.e., converted to cenobamate monotherapy or reduced from multiple to one concomitant ASM) between baseline and the last visit. Effectiveness, tolerability, and dosage of cenobamate were evaluated. Responses according to therapeutic regimen at last visit were studied.

resultsOf 694 patients within cenobamate EAPs, 75 (10.7%) met the inclusion criteria (mean age 39.5 years [range 19-65]). At baseline, the median number of prior ASMs was 10 (interquartile range [IQR] 6-13); 46 patients (61.3%) were taking two, 23 (30.7%) were taking three, and six (8%) were taking four concomitant ASMs at baseline. At the last visit, seven patients (9.3%) were converted to monotherapy and 68 (90.7%) were receiving one concomitant ASM. The median cenobamate dosage at last visit was 300 mg (IQR 200-350). Median cenobamate follow-up was 22 months; 73 patients (97%) had at least 1 year of follow-up and one discontinued cenobamate at 1 year. Twenty-five patients (33.3%) were seizure-free at last visit; 51 (68%) had a ≥50% reduction in seizure frequency. The seizure-freedom rate was numerically, but not significantly, higher in patients converted to monotherapy (57.1%) versus those receiving one concomitant ASM (30.9%; p = 0.16). Cenobamate plus clobazam was the most effective combination. Adverse events (AEs) were reported in 55/75 patients (73.3%); the most common were somnolence (30.7%), dizziness/vertigo (28%), and fatigue (26.7%). No AEs led to treatment discontinuation. SIGNIFICANCE: Cenobamate demonstrated good effectiveness and tolerability in a population of patients within European EAPs who achieved a significant reduction of concomitant ASM. PLAIN LANGUAGE SUMMARY: People with highly drug-resistant epilepsy often need to take several antiseizure medications at the same time. Combined data from European Early Access Programs show that about 10% of people treated with cenobamate were able to stop all other antiseizure medications or reduce treatment to cenobamate plus one other medication. Despite this simplification of treatment, one-third of these patients became seizure-free and more than two-thirds experienced at least a 50% reduction in seizure frequency. Within this group, no patients stopped cenobamate because of side effects.

Indexed as

cenobamate monotherapydual therapyreal‐world evidence

Identifiers

PMID42625556
PMCPMC13494722

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.