Ferrari Michel D, Wilkinson Marcia, Hirt Dorothea, Lataste Xavier, Notter Marianne
Department of Neurology, University Hospital, LeidenThe Netherlands The City of London Migraine Clinic, LondonU.K. Clinical Research, Sandoz Pharma Ltd., BasleSwitzerland.
Pain. 1991 Jun;45(3):283-291. doi: 10.1016/0304-3959(91)90052-Y.
To investigate whether the novel, potent and highly selective 5-hydroxytryptamine3 (5-HT3) receptor antagonist ICS 205-930 can prevent migraine attacks, we conducted simultaneously two randomized, double-blind, placebo-controlled, multicentre, international trials, involving a total of 204 patients, suffering from classic or common migraine. Both trials had the same parallel-group design (1 month baseline observation, followed by 3 months treatment) and both produced remarkably similar results. The primary efficacy parameter was the proportional reduction in attack frequency recorded after 3 months of treatment. Twenty-two patients withdrew prematurely from the trials and could not be assessed for efficacy. Mild to severe constipation was reported by about 50% of the patients on active treatment. None of the doses of ICS 205-930 tested (50 mg, 25 mg and 15 mg daily) produced a statistically significantly better result to reduce attack frequency than did placebo. However, confidence intervals for the difference in effect with placebo were wide, indicating that 15 mg ICS 205-930 may produce a 57% reduction in attack frequency as compared to placebo. The most unusual finding was that, for all efficacy parameters, the best results were obtained with the lowest dose (15 mg), the worst results with the highest dose (50 mg) and an intermediate effect with 25 mg. Such an inverse relation between dose and efficacy suggests a bell-shaped dose-response curve, implying that doses lower than 15 mg might well prove to be more effective. Thus, the present study has produced inconclusive, but intriguing results. Lower doses should be further investigated before drawing any definite conclusion on the efficacy of ICS 205-930 in the prophylactic treatment of migraine.
为研究新型、强效且高选择性的5-羟色胺3(5-HT3)受体拮抗剂ICS 205-930是否能预防偏头痛发作,我们同时进行了两项随机、双盲、安慰剂对照、多中心、国际试验,共纳入204例患有典型或普通偏头痛的患者。两项试验均采用相同的平行组设计(1个月基线观察,随后3个月治疗),且结果非常相似。主要疗效参数为治疗3个月后记录的发作频率的比例降低。22例患者提前退出试验,无法评估疗效。接受活性治疗的患者中约50%报告有轻度至重度便秘。所测试的ICS 205-930的任何剂量(每日50 mg、25 mg和15 mg)在降低发作频率方面均未产生统计学上显著优于安慰剂的结果。然而,与安慰剂相比,疗效差异的置信区间较宽,表明与安慰剂相比,15 mg ICS 205-930可能使发作频率降低57%。最不寻常的发现是,对于所有疗效参数,最低剂量(15 mg)获得最佳结果,最高剂量(50 mg)获得最差结果,25 mg产生中等效果。剂量与疗效之间的这种反比关系表明存在钟形剂量反应曲线,这意味着低于15 mg的剂量可能更有效。因此,本研究结果尚无定论,但很有趣。在对ICS 205-930在偏头痛预防性治疗中的疗效得出任何明确结论之前,应进一步研究更低剂量。