Effectiveness of perampanel as the only add-on: Retrospective, multicenter, observational real-life study on epilepsy

Sara Gasparini1,2, Edoardo Ferlazzo1,2,3, Sabrina Neri1,2

  • 1Department of Medical and Surgical Sciences, Magna Græcia University of Catanzaro, Catanzaro, Italy.

Epilepsia Open
|September 9, 2022
PubMed

Insights

Perampanel (PER) is an effective add-on treatment for epilepsy, showing high retention rates and seizure control in real-world use. Adverse events were less common than in clinical trials, confirming PER

Area of Science:

  • Epilepsy research
  • Pharmacology
  • Clinical neurology

Background:

  • Perampanel (PER) is an adjunctive antiseizure medication (ASM) for epilepsy.
  • Clinical trial data show PER's efficacy and tolerability.
  • Limited real-world data exist on PER as an only add-on treatment.

Purpose of the Study:

  • To evaluate the real-world effectiveness and safety of PER.
  • To assess PER's retention rate, seizure frequency, and adverse events.
  • To investigate PER's use as the sole add-on therapy for epilepsy.

Main Methods:

  • Observational, retrospective, multicenter study.
  • 503 patients with focal or generalized epilepsy (>12 years) received PER as the only add-on ASM.
  • Data collected at 3, 6, and 12 months on retention, seizure frequency, and adverse events.

Main Results:

  • High retention rate (89% at 12 months).
  • Early add-on PER use correlated with higher seizure freedom rates at 3 months (66% vs 53%).
  • Treatment-emergent adverse events occurred in 25% of patients, lower than in trials.

Conclusions:

  • Confirms PER's efficacy and safety in real-world epilepsy treatment.
  • Demonstrates effectiveness as an only add-on therapy, even in patients with long-standing epilepsy.
  • Provides robust data supporting PER's clinical utility.
Abstract

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