a Inserm NeuroDiderot , InDev , Paris , France.
b Neurospin , CEA , Paris , France.
Expert Rev Neurother. 2019 Apr;19(4):301-310. doi: 10.1080/14737175.2019.1593142. Epub 2019 Apr 2.
Stiripentol is an orphan drug approved for the treatment of seizures associated with Dravet syndrome (since 2007 in Europe). Therapeutic options recently grew in this rare and severe early-onset epilepsy with the approval of stiripentol and cannabidiol in 2018 in the US and the positive trials just completed with fenfluramine. Areas covered: First, the short-term efficacy of stiripentol as adjunctive therapy to clobazam and valproate, which was discovered by serendipity thanks to a basket study and then confirmed in 1998 despite the small number of samples in phase III trials. Second, the further observational series worldwide, which showed sustained efficacy and satisfactory tolerability for up to 20 year exposure. Third, why it took more than 20 years for stiripentol be approved in a number of countries despite these extensive data: drug-drug interactions between stiripentol and comedication will be addressed, as well as the experimental and pharmacogenetic data which support the anticonvulsant effect of stiripentol per se. Expert opinion: Considering current and future competitors (cannabidiol and fenfluramine), efficacy seems lower for cannabidiol and seizure freedom seems occasionally be obtained with fenfluramine. Additionally, stiripentol could be especially useful in two critical conditions of the disease, very young age (<2 years) and convulsive status epilepticus.
司来吉兰是一种孤儿药,被批准用于治疗 Dravet 综合征相关的癫痫发作(自 2007 年以来在欧洲使用)。随着司来吉兰和大麻二酚于 2018 年在美国获得批准,以及刚刚完成的芬氟拉明阳性试验,这种罕见且严重的早发性癫痫的治疗选择最近有所增加。涵盖领域:首先,司来吉兰作为氯巴占和丙戊酸钠的辅助治疗的短期疗效,这是通过一项篮子研究偶然发现的,然后在 1998 年得到证实,尽管在 III 期临床试验中样本数量较少。其次,全球范围内的进一步观察性系列研究表明,在长达 20 年的暴露中,司来吉兰具有持续的疗效和良好的耐受性。第三,尽管有这些广泛的数据,为什么司来吉兰在多个国家的批准花了 20 多年的时间:将讨论司来吉兰与合并用药之间的药物相互作用,以及支持司来吉兰本身抗惊厥作用的实验和遗传药理学数据。专家意见:考虑到当前和未来的竞争对手(大麻二酚和芬氟拉明),大麻二酚的疗效似乎较低,而芬氟拉明似乎偶尔可以使癫痫发作得到控制。此外,司来吉兰在疾病的两种关键情况下可能特别有用,即非常年幼(<2 岁)和癫痫持续状态。