Safety and effectiveness of perampanel monotherapy after adjunctive therapy through retention rate in subjects with focal-onset seizures with or without focal to bilateral tonic-clonic seizures: A multicenter retrospective study in Koreaopen access
- Authors
- Lim, Sung Chul; Lee, Won Gu; Kim, Dong Wook; Kim, Kwang Ki; Shon, Young-Min; Park, Jihyun; Lee, Yoona; Seo, Dae-Won
- Issue Date
- Aug-2023
- Publisher
- Elsevier Inc
- Keywords
- Perampanel; Monotherapy; Antiepileptic drug; Focal -onset seizures; Retention rate
- Citation
- Epilepsy & Behavior, v.145, pp 1 - 5
- Pages
- 5
- Indexed
- SCIE
SCOPUS
- Journal Title
- Epilepsy & Behavior
- Volume
- 145
- Start Page
- 1
- End Page
- 5
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/21149
- DOI
- 10.1016/j.yebeh.2023.109291
- ISSN
- 1525-5050
1525-5069
- Abstract
- Objective: To assess the effectiveness and tolerability of perampanel monotherapy following conversion from adjunctive therapy. Methods: This was a multicenter, retrospective, non-interventional study of Korean patients aged & GE;12 years with focal-onset seizures (FOS) with or without focal to bilateral tonic-clonic seizures. Data were extracted from electronic medical records of perampanel-treated patients from 1 February 2016 to 31 October 2020. Kaplan-Meier estimated retention rates, effectiveness, and safety were recorded. Results: Subjects (n = 66, mean age 46.2 years) were mostly male (68.2%) with focal to bilateral tonic-clonic seizure (71.2%). Mean duration of illness was 86.3 months. Retention rates after conversion to per-ampanel monotherapy at 3, 6, and 12 months (primary outcome) were 96.0%, 96.0%, and 75.6%, respec-tively. Overall retention rates in patients receiving perampanel as adjunctive or monotherapy at 3, 6, 12, 18, and 24 months after perampanel add-on were 100%, 98.3%, 95.9%, 92.6%, and 92.6%, respectively. Mean retention duration was 41.2 months (overall perampanel administration) and 21.4 months (monotherapy). Mean seizure frequency/28 days in the Full Analysis Set (n = 61) was comparable for adjunctive and monotherapy (0.2 & PLUSMN; 0.79 vs 0.2 & PLUSMN; 0.64; change between adjunctive and monotherapy peri-ods: 0.0 & PLUSMN; 0.59; p = 0.498). Perampanel was well tolerated and no new safety signals were identified. Dizziness (4.6%), only reported during adjunctive therapy, was the most common treatment-emergent adverse event. Conclusions: Conversion to perampanel monotherapy from adjunctive therapy showed promising results in subjects with FOS with/without focal to bilateral tonic-clonic seizures; further studies in a larger pop-ulation are needed to confirm these encouraging data. & COPY; 2023 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
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