Perampanel for the treatment of Asian people with epilepsy: Real-world evidence from the PERMIT extension study

IF 3.6 3区 医学 Q1 CLINICAL NEUROLOGY Journal of the Neurological Sciences Pub Date : 2024-08-14 DOI:10.1016/j.jns.2024.123173
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Abstract

This post-hoc analysis of the PERMIT Extension study compared the effectiveness and safety/tolerability of perampanel (PER) between Asian and non-Asian participants. Retention rates, adverse events (AEs), seizure frequency, responder rate (≥50% seizure frequency reduction), and seizure freedom rate (no seizures since at least the prior visit) were assessed. Retention was assessed after 3, 6 and 12 months. Effectiveness assessments were evaluated at 3, 6 and 12 months and the last visit by seizure type (total, focal and generalised). PERMIT Extension included 730 Asian and 1662 non-Asian individuals. Significant differences in demographic/baseline characteristics were reported for the Asian versus non-Asian subgroups including higher median age at epilepsy onset, longer median duration of epilepsy, higher mean number of previous and concomitant ASMs and lower mean monthly seizure frequency (total, focal and generalised). Retention rates were similar between the two subgroups at 3 and 12 months, but significantly lower in the Asian versus non-Asian subgroup at 6 months (65.6% vs. 71.8%; p = 0.004). At last visit, seizure freedom rate was significantly higher in the Asian versus non-Asian for total (35.9% vs. 25.4%; p = 0.001) and focal seizures (32.4% vs. 18.9%; p = 0.001) as was responder rate for both total (63.9% vs. 52.3%; p = 0.001) and focal seizures (62.2% vs. 44.7%; p < 0.001). Seizure freedom and responder rates for generalised seizures were similar between the two subgroups at the last visit. Rates of AEs were similar between the two subgroups (Asian, 47.6%; non-Asian, 45.4%). PER was effective and generally well-tolerated in Asian and non-Asian individuals.

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佩兰帕奈用于治疗亚洲癫痫患者:来自 PERMIT 扩展研究的现实世界证据
这项 PERMIT 扩展研究的事后分析比较了亚裔和非亚裔参与者服用培南帕奈(PER)的有效性和安全性/耐受性。研究评估了保留率、不良事件(AEs)、癫痫发作频率、应答率(癫痫发作频率减少≥50%)和癫痫发作自由率(至少自前次就诊以来无癫痫发作)。3个月、6个月和12个月后对保留率进行评估。疗效评估在 3、6 和 12 个月以及最后一次就诊时按癫痫发作类型(总体性、局灶性和全身性)进行。PERMIT 推广项目包括 730 名亚洲人和 1662 名非亚洲人。据报道,亚裔与非亚裔亚组在人口统计学/基线特征方面存在显著差异,包括癫痫发病年龄中位数较高、癫痫持续时间中位数较长、既往和并发 ASM 的平均次数较高以及每月平均发作频率(总体、局灶性和全身性)较低。两个亚组在 3 个月和 12 个月的保留率相似,但在 6 个月时,亚裔亚组的保留率明显低于非亚裔亚组(65.6% 对 71.8%;P = 0.004)。在最后一次就诊时,亚裔与非亚裔的总发作自由度(35.9% vs. 25.4%;p = 0.001)和局灶发作自由度(32.4% vs. 18.9%;p = 0.001)均显著高于非亚裔,总发作自由度(63.9% vs. 52.3%;p = 0.001)和局灶发作自由度(62.2% vs. 44.7%;p <0.001)的应答率也显著高于非亚裔。在最后一次就诊时,两个亚组的癫痫发作自由度和全身性癫痫发作应答率相似。两个亚组的AEs发生率相似(亚裔为47.6%;非亚裔为45.4%)。PER对亚裔和非亚裔患者均有效,且耐受性普遍良好。
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来源期刊
Journal of the Neurological Sciences
Journal of the Neurological Sciences 医学-临床神经学
CiteScore
7.60
自引率
2.30%
发文量
313
审稿时长
22 days
期刊介绍: The Journal of the Neurological Sciences provides a medium for the prompt publication of original articles in neurology and neuroscience from around the world. JNS places special emphasis on articles that: 1) provide guidance to clinicians around the world (Best Practices, Global Neurology); 2) report cutting-edge science related to neurology (Basic and Translational Sciences); 3) educate readers about relevant and practical clinical outcomes in neurology (Outcomes Research); and 4) summarize or editorialize the current state of the literature (Reviews, Commentaries, and Editorials). JNS accepts most types of manuscripts for consideration including original research papers, short communications, reviews, book reviews, letters to the Editor, opinions and editorials. Topics considered will be from neurology-related fields that are of interest to practicing physicians around the world. Examples include neuromuscular diseases, demyelination, atrophies, dementia, neoplasms, infections, epilepsies, disturbances of consciousness, stroke and cerebral circulation, growth and development, plasticity and intermediary metabolism.
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