Relja M, Poole A C, Schoenen J, Pascual J, Lei X, Thompson C
Department of Neurology, Medical School University of Zagreb, Zagreb, Croatia.
Cephalalgia. 2007 Jun;27(6):492-503. doi: 10.1111/j.1468-2982.2007.01315.x. Epub 2007 Apr 11.
Our aim was to evaluate the safety and efficacy of botulinum toxin type A (BoNTA; BOTOX) for prophylaxis of episodic migraine. In this double-blind, placebo-controlled study, patients were randomized to 225, 150 or 75 U of BoNTA or placebo after a 30-day placebo run-in for three 90-day treatment cycles. The primary efficacy end-point was the mean reduction from baseline in the frequency of migraine episodes at day 180 in the placebo non-responder stratum. All groups (N = 495) improved, with no significant differences. At day 180, the frequency of migraine episodes was reduced from baseline means of 4.3, 4.7, 4.7 and 4.4 by 1.6, 1.7, 1.5 and 1.4 for BoNTA 225 U, 150 U and 75 U and placebo, respectively. The primary end-point was not met. Treatment-related adverse events were transient and mild to moderate. BoNTA treatment was safe and well tolerated but did not result in significantly greater improvement than placebo in this study. Several factors may have confounded the results.
我们的目的是评估A型肉毒毒素(BoNTA;保妥适)预防发作性偏头痛的安全性和有效性。在这项双盲、安慰剂对照研究中,患者在经过30天的安慰剂导入期后,被随机分为接受225单位、150单位或75单位的BoNTA治疗或安慰剂治疗,为期三个90天的治疗周期。主要疗效终点是安慰剂无反应者亚组在第180天时偏头痛发作频率相对于基线的平均降低幅度。所有组(N = 495)均有改善,无显著差异。在第180天时,225单位、150单位和75单位的BoNTA组以及安慰剂组的偏头痛发作频率相对于基线均值4.3、4.7、4.7和4.4分别降低了1.6、1.7、1.5和1.4。主要终点未达到。治疗相关不良事件为短暂性,且为轻至中度。在本研究中,BoNTA治疗安全且耐受性良好,但与安慰剂相比,并未带来显著更大的改善。可能有几个因素混淆了结果。