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Early Cenobamate as a Third-Line Option in Drug-Resistant Focal Epilepsy: A Paradigm Shift?

  • Fedele Dono
  • , Mirella Russo
  • , Rita Agosto
  • , Giacomo Evangelista
  • , Bruna Nucera
  • , Giovanni Falcicchio
  • , Stefano L Sensi
  • University "G. d'Annunzio" of Chieti-Pescara
  • Hospital of Merano-Meran (SABES-ASDAA)
  • University "Aldo Moro" of Bari

Research output: Contribution to journal › Original Article › peer-review

Abstract

IntroductionDrug-resistant epilepsy (DRE) affects nearly 30% of patients with epilepsy, and the optimal sequencing of adjunctive anti-seizure medications (ASMs) remains uncertain. Comparative real-world evidence on early use of newer ASM is limited. This study explores real-world comparative effectiveness, safety and 12-month retention of cenobamate (CNB) introduced as early third-line adjunctive therapy compared with perampanel (PER) and brivaracetam (BRV) in adults with focal-onset DRE.MethodsThis multicenter observational study included 34 CNB patients and 37 matched controls treated with PER or BRV, all after failure of two prior ASMs. Primary outcome was 12-month treatment retention; secondary outcomes included responder rates (>= 50%, >= 75%, 100%) and adverse events at 3, 6 and 12 months. Comparative analyses were exploratory. Univariate analyses and longitudinal generalized linear mixed-effects models (GLMMs) were used to describe outcome trajectories over time.ResultsCNB showed a 12-month retention rate of 94.1%. Descriptively, seizure freedom was achieved in 62.5% of CNB patients at 12 months compared with 43.7% with PER and 16.6% with BRV. Adverse events were less frequent with CNB (9.4% at 12 months) than in controls (35.3%) and were generally non-treatment-limiting. GLMMs confirmed a significant time & times; treatment interaction for seizure frequency, indicating a steeper reduction in CNB patients, while no significant interaction emerged for adverse events.ConclusionsIn this real-world study, early third-line CNB exhibits potentially favorable effectiveness compared with other commonly used third-line ASMs, and tolerability remained acceptable. These findings support the need for larger prospective studies to better define optimal treatment sequencing in focal-onset DRE.
Original languageEnglish
Pages (from-to)1191-1205
Number of pages15
JournalNEUROLOGY AND THERAPY
Volume15
Issue number3
Early online dateMar 2026
DOIs
Publication statusPublished - Jun 2026

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