Efficacy and safety of perampanel in generalized and focal to bilateral tonic-clonic seizures: A comparative study of Asian and non-Asian populations

被引:15
|
作者
Nishida, Takuji [1 ]
Lee, Sang Kun [2 ]
Wu, Tony [3 ]
Tiamkao, Somsak [4 ]
Dash, Amitabh [5 ]
机构
[1] Natl Hosp Org, Shizuoka Inst Epilepsy & Neurol Disorders, Natl Epilepsy Ctr, Shizuoka, Japan
[2] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Neurol, Coll Med, Seoul, South Korea
[3] Chang Gung Mem Hosp & Univ, Dept Neurol, Taoyuan, Taiwan
[4] Khon Kaen Univ, Dept Med, Integrated Epilepsy Res Grp, Fac Med, Khon Kaen, Thailand
[5] Eisai Singapore Pte Ltd, Singapore, Singapore
关键词
antiepileptic drugs; Asian; focal seizures; focal to bilateral tonic-clonic seizures; generalized tonic-clonic seizures; SUDDEN UNEXPECTED DEATH; RANDOMIZED PHASE-III; QUALITY-OF-LIFE; ADJUNCTIVE PERAMPANEL; LONG-TERM; EPILEPSY; ONSET; MORTALITY; FREQUENCY; ACCIDENTS;
D O I
10.1111/epi.14644
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Perampanel is an approved adjunctive treatment for focal seizures with or without focal to bilateral tonic-clonic (FBTC) seizures and generalized tonic-clonic (GTC) seizures. We compared efficacy and safety of perampanel vs placebo in Asian and non-Asian populations in a post hoc analysis of pooled data from 5 randomized phase 3 studies. Patients (>= 12 years old) with focal + FBTC seizures received perampanel 2, 4, 8, or 12 mg or placebo; patients with GTC seizures received perampanel 8 mg or placebo (titration: 4-6 weeks; maintenance: 13 weeks). Efficacy endpoints included median percentage change in FBTC or GTC seizure frequency per 28 days and 50% responder rate relative to baseline. Median percentage change in FBTC seizure frequency was significantly greater for perampanel 8 and 12 mg than placebo in the Asian population (median difference from placebo: -30.32%, P = 0.0017; -30.06%, P = 0.0008, respectively) and perampanel 4, 8, and 12 mg in the non-Asian population (-35.07%, P = 0.0001; -37.78%, P < 0.0001; -34.53%, P < 0.0001, respectively). In both populations, median percentage change in GTC seizure frequency was significantly greater for perampanel 8 mg than placebo (median difference from placebo: Asian, -37.37%, P = 0.0139; non-Asian, -27.04%, P = 0.0006). The 50% responder rates were significantly greater than placebo for perampanel 8 and 12 mg for FBTC seizures (Asian: 58.0%, P = 0.0017 and 58.6%, P = 0.0013, respectively; non-Asian: 59.3%, P < 0.0001 and 54.3%, P = 0.0050, respectively) and perampanel 8 mg for GTC seizures (Asian: 57.6%, P = 0.0209; non-Asian: 68.8%, P = 0.0329). Pooled FBTC/GTC seizure data showed generally similar patterns of response to perampanel in both populations. The most frequent treatment-related adverse events were fatigue, irritability, dizziness, somnolence, and headache. Perampanel was effective, well tolerated, and can be considered a therapeutic option for FBTC/GTC seizures in Asian populations.
引用
收藏
页码:47 / 59
页数:13
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