Efficacy, safety, and tolerability of perampanel in Asian and non-Asian patients with epilepsy

被引:18
作者
Tsai, Jing-Jane [1 ,2 ]
Ikeda, Akio [3 ]
Hong, Seung Bong [4 ,5 ]
Likasitwattanakul, Surachai [6 ]
Dash, Amitabh [7 ]
机构
[1] Natl Cheng Kung Univ Hosp, Dept Neurol, Tainan, Taiwan
[2] Natl Cheng Kung Univ, Sch Med, Tainan, Taiwan
[3] Kyoto Univ, Grad Sch Med, Dept Epilepsy Movement Disorders & Physiol, Kyoto, Japan
[4] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Dept Neurol,Samsung Med Ctr, Seoul, South Korea
[5] Sungkyunkwan Univ, Sch Med, Samsung Adv Inst Hlth Sci & Technol, Seoul, South Korea
[6] Mahidol Univ, Dept Pediat, Fac Med, Bangkok, Thailand
[7] Eisai Singapore Pte Ltd, Singapore, Singapore
关键词
antiepileptic drugs; Asian; epilepsy; focal seizures; perampanel; SEIZURES INTEGRATED ANALYSIS; REFRACTORY PARTIAL SEIZURES; RANDOMIZED PHASE-III; ADJUNCTIVE PERAMPANEL; DOUBLE-BLIND; PARALLEL-GROUP; ADULT PATIENTS; MULTICENTER; RETIGABINE; TOPIRAMATE;
D O I
10.1111/epi.14642
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
People of different ethnic or racial backgrounds may experience variations in pharmacokinetic and pharmacodynamic responses to drug therapies. Our post hoc analysis evaluated the efficacy, safety, and tolerability of perampanel in Asian and non-Asian populations with refractory focal seizures with or without focal to bilateral tonic-clonic (FBTC) seizures. This analysis pooled data from 4 randomized, placebo-controlled, phase-3 studies involving patients aged >= 12 years who have focal seizures with or without FBTC seizures. Patients were receiving 2, 4, 8, or 12 mg perampanel (or placebo) by the end of a 6-week titration period and for a further 13 weeks during the maintenance phase. Efficacy endpoints included median percent change in seizure frequency per 28 days, and 50% and seizure-freedom responder rates relative to baseline. The median percent change in seizure frequency per 28 days from baseline was significantly greater than placebo for perampanel 8 and 12 mg (-31.1% and -38.1% change, respectively; each P < 0.0001) in the Asian population, and for perampanel 4, 8, and 12 mg (-21.1% [P = 0.0001], -26.3% [P < 0.0001], and -27.7% [P = 0.0001] change, respectively) in the non-Asian population. The 50% responder rate relative to baseline was significantly greater than placebo for perampanel 8 and 12 mg (40.1% and 43.8%, respectively; each P < 0.0001) in the Asian population, and for perampanel 4, 8, and 12 mg (29.4% [P = 0.0002], 32.8% [P < 0.0001] and 34.5% [P = 0.0001]), respectively, in the non-Asian population. Seizure-freedom rate among all patients was 4.9%-11.7% for perampanel 2, 4, 8, and 12 mg. The most frequently reported treatment-emergent adverse events (TEAEs) across both populations were dizziness, somnolence, irritability, headache, and fatigue. The most common psychiatric TEAEs were aggression and irritability. Perampanel demonstrated a favorable and similar risk-benefit profile in both Asian and non-Asian populations with refractory focal seizures.
引用
收藏
页码:37 / 46
页数:10
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