Privitera M D
Department of Neurology, College of Medicine, University of Cincinnati Medical Center, OH 45267, USA.
Ann Pharmacother. 1997 Oct;31(10):1164-73. doi: 10.1177/106002809703101010.
To review proposed mechanisms of action, clinical pharmacology, efficacy, safety, and tolerability of the antiepileptic drug (AED) topiramate.
All available data from the clinical development program--published and unpublished data (provided by investigators or the RW Johnson Pharmaceutical Research Institute)--were analyzed, with emphasis on the results of double-blind, placebo-controlled trials. Data from open-label studies provided information about long-term efficacy and tolerability.
Topiramate is highly effective in the control of previously therapy-resistant partial seizures, with or without secondary generalization. In the refractory adult patient population enrolled in controlled clinical trials, seizures were reduced by 50% or more in 27-47% of patients compared with 0-18% in placebo-treated patients and by 75% or more in 9-36% of the patients compared with 0-9% of those receiving placebo. The most common adverse effects involve the central nervous system and are mild to moderate in nature. Adverse effects include somnolence, fatigue, psychomotor slowing, and concentration problems. The currently recommended dosing is lower and titration slower than schedules used in the clinical trials; this may improve the tolerability of topiramate. Topiramate has few interactions with currently available AEDs, but phenytoin concentrations increased in some patients. Topiramate can be used initially as adjunctive therapy. Plasma topiramate concentrations are reduced substantially when used with enzyme-inducing AEDs. Open-label data and a single double-blind trial suggest that topiramate monotherapy may be effective. Open-label data also indicate that topiramate may be effective in generalized seizures of nonfocal origin, including those associated with Lennox-Gastaut syndrome.
The robust clinical effects of topiramate expand the therapeutic options for patients with epilepsy. Controlled clinical trials are needed to verify initial observations that topiramate may be effective against a broad spectrum of seizure types and to directly compare efficacy and tolerability with other new and standard AEDs.
综述抗癫痫药物托吡酯的作用机制、临床药理学、疗效、安全性及耐受性。
分析临床研发项目的所有可用数据,包括已发表和未发表的数据(由研究者或强生制药研究所提供),重点关注双盲、安慰剂对照试验的结果。开放标签研究的数据提供了关于长期疗效和耐受性的信息。
托吡酯对先前治疗耐药的部分性发作有效,无论是否伴有继发性全面发作。在纳入对照临床试验的难治性成年患者群体中,27% - 47%的患者癫痫发作减少了50%或更多,而安慰剂治疗组为0% - 18%;9% - 36%的患者癫痫发作减少了75%或更多,而接受安慰剂治疗的患者为0% - 9%。最常见的不良反应累及中枢神经系统,性质为轻至中度。不良反应包括嗜睡、疲劳、精神运动迟缓及注意力不集中问题。目前推荐的给药剂量低于临床试验中的剂量,滴定速度也较慢;这可能会提高托吡酯的耐受性。托吡酯与目前可用的抗癫痫药物相互作用较少,但部分患者的苯妥英浓度升高。托吡酯最初可作为辅助治疗使用。与酶诱导性抗癫痫药物合用时,托吡酯的血浆浓度会大幅降低。开放标签数据和一项双盲试验表明托吡酯单药治疗可能有效。开放标签数据还表明托吡酯对非局灶性起源的全身性发作可能有效,包括与伦诺克斯 - 加斯托综合征相关的发作。
托吡酯强大的临床疗效为癫痫患者扩展了治疗选择。需要进行对照临床试验来验证托吡酯可能对广泛的癫痫发作类型有效的初步观察结果,并直接将其疗效和耐受性与其他新型和标准抗癫痫药物进行比较。