Epilepsy Unit, Western Infirmary, Glasgow, Scotland, UK.
Neurology. 2010 Nov 16;75(20):1817-24. doi: 10.1212/WNL.0b013e3181fd6170. Epub 2010 Oct 13.
This study assessed the efficacy and safety of the neuronal potassium channel opener ezogabine (US adopted name; EZG)/retigabine (international nonproprietary name; RTG) as adjunctive therapy for refractory partial-onset seizures.
This was a multicenter, randomized, double-blind, placebo-controlled trial in adults with ≥4 partial-onset seizures per month receiving 1 to 3 antiepileptic drugs. EZG (RTG) or placebo, 3 times daily, was titrated to 600 or 900 mg/d over 4 weeks, and continued during a 12-week maintenance phase. Median percentage seizure reductions from baseline and responder rates (≥50% reduction in baseline seizure frequency) were assessed.
The intention-to-treat population comprised 538 patients (placebo, n = 179; 600 mg, n = 181; 900 mg, n = 178), 471 of whom (placebo, n = 164; 600 mg, n = 158; 900 mg, n = 149) entered the maintenance phase. Median percentage seizure reductions were greater in EZG (RTG)-treated patients (600 mg, 27.9%, p = 0.007; 900 mg, 39.9%, p < 0.001) compared with placebo (15.9%). Responder rates were higher in EZG (RTG)-treated patients (600 mg, 38.6%, p < 0.001; 900 mg, 47.0%, p < 0.001) than with placebo (18.9%). Treatment discontinuations due to adverse events (AEs) were more likely with EZG (RTG) than with placebo (placebo, 8%; 600 mg, 17%, 900 mg, 26%). The most commonly reported (>10%) AEs in the placebo, EZG (RTG) 600 mg/d, and EZG (RTG) 900 mg/d groups were dizziness (7%, 17%, 26%), somnolence (10%, 14%, 26%), headache (15%, 11%, 17%), and fatigue (3%, 15%, 17%).
In this dose-ranging, placebo-controlled trial, adjunctive EZG (RTG) was effective and generally well tolerated in adults with refractory partial-onset seizures.
This study provides Class II evidence that adjunctive EZG/RTG reduces the occurrence of partial-onset seizures.
本研究评估神经元钾通道 opener 依佐加滨(美国采用名;EZG)/瑞替加滨(国际非专利名;RTG)作为辅助治疗难治性部分发作性癫痫的疗效和安全性。
这是一项多中心、随机、双盲、安慰剂对照试验,纳入每月有≥4 次部分发作性癫痫且正在接受 1 至 3 种抗癫痫药物治疗的成年人。EZG(RTG)或安慰剂每日 3 次滴定,4 周内滴定至 600 或 900 mg/d,在 12 周的维持期继续治疗。评估基线时的中位癫痫发作减少百分比和应答率(基线癫痫发作频率减少≥50%)。
意向治疗人群包括 538 例患者(安慰剂,n=179;600 mg,n=181;900 mg,n=178),其中 471 例(安慰剂,n=164;600 mg,n=158;900 mg,n=149)进入维持期。与安慰剂(15.9%)相比,EZG(RTG)治疗患者的中位癫痫发作减少百分比更大(600 mg,27.9%,p=0.007;900 mg,39.9%,p<0.001)。EZG(RTG)治疗患者的应答率更高(600 mg,38.6%,p<0.001;900 mg,47.0%,p<0.001),安慰剂(18.9%)。因不良事件(AE)而停药的情况在 EZG(RTG)治疗患者中比安慰剂更常见(安慰剂,8%;600 mg,17%;900 mg,26%)。安慰剂、EZG(RTG)600 mg/d 和 EZG(RTG)900 mg/d 组中报告发生率>10%的最常见 AE 为头晕(7%、17%、26%)、嗜睡(10%、14%、26%)、头痛(15%、11%、17%)和疲劳(3%、15%、17%)。
在这项剂量范围的安慰剂对照试验中,辅助性 EZG(RTG)在难治性部分发作性癫痫成人中是有效且通常耐受良好的。
本研究提供了 II 级证据,表明辅助性 EZG/RTG 可减少部分发作性癫痫的发生。