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CNS Drugs. 2014 Jul;28(7):583-600. doi: 10.1007/s40263-014-0182-2.
Eslicarbazepine acetate (Aptiom(®), Zebinix(®)) is approved for the adjunctive treatment of partial-onset seizures in adults aged ≥18 years. Adjunctive therapy with oral eslicarbazepine acetate 800 or 1,200 mg once daily was associated with a significantly lower standardized seizure frequency (primary endpoint) than placebo in patients aged ≥18 years with refractory partial-onset seizures in three, randomized, double-blind, multinational, phase III trials. In a fourth randomized, double-blind, multinational, phase III trial in patients aged ≥16 years with refractory partial-onset seizures, adjunctive eslicarbazepine acetate 1,200 mg once daily, but not 800 mg once daily, was associated with a significantly lower standardized seizure frequency (primary endpoint). Responder rates were significantly higher with eslicarbazepine acetate 1,200 mg once daily than with placebo in these four trials, and with eslicarbazepine acetate 800 mg once daily than with placebo in two trials. The efficacy of eslicarbazepine acetate was maintained in the longer term, according to the results of 1-year extension studies. Adjunctive therapy with oral eslicarbazepine acetate was generally well tolerated in patients with refractory partial-onset seizures, with most adverse events being of mild to moderate severity. In conclusion, eslicarbazepine acetate is a useful option for the adjunctive treatment of patients with refractory partial-onset seizures.
依沙佐匹坦醋酸酯(Aptiom(®),Zebinix(®))被批准用于辅助治疗 18 岁及以上成人部分发作性癫痫。在三项随机、双盲、多中心、III 期临床试验中,对于难治性部分发作性癫痫患者,每日口服依沙佐匹坦醋酸酯 800 或 1200mg 作为辅助治疗与安慰剂相比,显著降低了标准化癫痫发作频率(主要终点)。在一项纳入 16 岁及以上难治性部分发作性癫痫患者的随机、双盲、多中心、III 期的第四次临床试验中,每日口服依沙佐匹坦醋酸酯 1200mg 作为辅助治疗与安慰剂相比,显著降低了标准化癫痫发作频率(主要终点)。与安慰剂相比,每日口服依沙佐匹坦醋酸酯 1200mg 的患者应答率显著更高,在这四项试验中,每日口服依沙佐匹坦醋酸酯 800mg 的患者应答率也显著高于安慰剂。根据为期 1 年的扩展研究结果,依沙佐匹坦醋酸酯的疗效在长期治疗中得以维持。对于难治性部分发作性癫痫患者,口服依沙佐匹坦醋酸酯辅助治疗总体耐受性良好,大多数不良事件为轻度至中度。总之,依沙佐匹坦醋酸酯是治疗难治性部分发作性癫痫患者的一种有效选择。