Assessment of the long-term efficacy and safety of adjunctive perampanel in tonic-clonic seizures: Analysis of four open-label extension studies

被引:18
作者
Rektor, Ivan [1 ,2 ]
Krauss, Gregory L. [3 ]
Inoue, Yushi [4 ]
Kaneko, Sunao [5 ]
Williams, Betsy [6 ]
Patten, Anna [7 ]
Malhotra, Manoj [6 ]
Laurenza, Antonio [6 ]
Wechsler, Robert T. [8 ]
机构
[1] Masaryk Univ, Brno Epilepsy Ctr, Kamenice 753-5, Brno 62500, Czech Republic
[2] Masaryk Univ, Cent European Inst Technol CEITEC, Kamenice 753-5, Brno 62500, Czech Republic
[3] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[4] Natl Epilepsy Ctr, Shizuoka Inst Epilepsy & Neurol Disorders, Shizuoka, Japan
[5] Minato Hosp, North Tohoku Epilepsy Ctr, Hachinohe, Aomori, Japan
[6] Eisai Inc, Woodcliff Lake, NJ USA
[7] Eisai Ltd, Hatfield, Herts, England
[8] Idaho Comprehens Epilepsy Ctr, Boise, ID USA
关键词
AMPA receptor antagonist; antiseizure medication; focal to bilateral tonic-clonic seizures; generalized tonic-clonic seizures; PARTIAL-ONSET SEIZURES; SUDDEN UNEXPECTED DEATH; IDIOPATHIC GENERALIZED EPILEPSY; RANDOMIZED PHASE-III; ANTIEPILEPTIC DRUGS; RISK; TOLERABILITY; CHILDREN; ABSENCE;
D O I
10.1111/epi.16573
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective This post hoc analysis evaluated long-term efficacy and safety in patients with focal to bilateral tonic-clonic seizures (FBTCS) or generalized tonic-clonic seizures (GTCS) who entered open-label extension (OLEx) studies to receive long-term adjunctive perampanel. Methods Patients aged 12 years and older who completed phase II or III randomized, double-blind, placebo-controlled studies could enter an OLEx study, each comprising a blinded conversion period followed by an open-label maintenance period (32-424 weeks; maximum perampanel dose = 12 mg/d). Exposure, seizure outcomes, and treatment-emergent adverse events (TEAEs) were analyzed. Results Baseline characteristics were generally balanced between patients with FBTCS (n = 720) and GTCS (n = 138). Mean (standard deviation) cumulative duration of perampanel exposure was 102.3 (70.3) weeks (FBTCS) and 83.9 (38.4) weeks (GTCS). Retention rates were 50.0% for up to 4 years (FBTCS) and 49.2% for up to 2 years (GTCS). Across OLEx treatment durations, median reductions in seizure frequency per 28 days were 66.7% (FBTCS) and 80.6% (GTCS). Fifty percent and 75% responder and seizure-freedom rates were 59.5%, 45.3%, and 18.4%, respectively (FBTCS), and 72.5%, 51.5%, and 16.7%, respectively (GTCS). Efficacy was sustained for up to 4 years (FBTCS) and up to 3 years (GTCS), even when accounting for early dropouts. TEAE incidence was highest during Year 1 (FBTCS, 85.3%; GTCS, 86.2%); most common were dizziness and somnolence. During Year 1, serious TEAEs were reported in 81 (11.3%; FBTCS) and 10 (7.2%; GTCS) patients. TEAEs were consistent with the known safety profile of perampanel; no new safety signals were identified with long-term treatment. Significance This post hoc analysis suggests long-term (up to 4 years) adjunctive perampanel (up to 12 mg/d) is efficacious and well tolerated in patients (aged 12 years and older) with FBTCS or GTCS.
引用
收藏
页码:1491 / 1502
页数:12
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