Bensimon G, Lacomblez L, Delumeau J C, Bejuit R, Truffinet P, Meininger V
Dept. Pharmacologie Clinique, Centre Hospitalier Universitaire Pitié-Salpêtrière, Assistance Publique Hôpitaux de Paris & Université Pierre & Marie Curie, 75013 Paris, France.
J Neurol. 2002 May;249(5):609-15. doi: 10.1007/s004150200071.
Treatment with the neuroprotective drug riluzole has previously been shown to increase the probability of survival in patients with amyotrophic lateral sclerosis. This report describes a placebo-controlled, double-blind randomised clinical trial of riluzole carried out in ALS patients with advanced stage disease or aged over 75 years. The primary objective was to enable access to treatment to patients excluded from the pivotal trial which was run in parallel. Another goal was to assess the safety of riluzole in patients with advanced-stage disease. One hundred and sixty-eight patients were included, randomised to either riluzole 50 mg b. i. d. or to placebo, and treated for eighteen months. Riluzole was well-tolerated in this patient population, and the adverse events observed were similar in nature and frequency to those observed in previously published clinical trials in patients included in pivotal trials. The study could not include enough patients to reach adequate power to detect differences in survival between the two treatment groups, and no such difference was in fact observed. In conclusion, riluzole is well-tolerated in ALS patients with advanced stage disease.
先前的研究表明,使用神经保护药物利鲁唑可提高肌萎缩侧索硬化症患者的存活几率。本报告描述了一项针对晚期疾病或年龄超过75岁的肌萎缩侧索硬化症患者开展的利鲁唑安慰剂对照双盲随机临床试验。主要目的是让被排除在同期进行的关键试验之外的患者能够接受治疗。另一个目标是评估利鲁唑在晚期疾病患者中的安全性。纳入了168名患者,随机分为接受每日两次50毫克利鲁唑治疗组或安慰剂组,并进行了18个月的治疗。在该患者群体中,利鲁唑耐受性良好,观察到的不良事件在性质和频率上与先前发表的关键试验中纳入的患者的临床试验中观察到的相似。该研究纳入的患者数量不足,无法获得足够的检验效能来检测两个治疗组之间的生存差异,实际上也未观察到此类差异。总之,利鲁唑在晚期疾病的肌萎缩侧索硬化症患者中耐受性良好。