[Botulinum toxin type A (Relatox) in the treatment of chronic migraine in adults: results of phase IIIb, randomized, one-blind, multicenter, active-controlled, parallel-group trial].

A R Artemenko, V G Abramov, Z N Konovalova, A N Korenko, D A Krasavina, A L Kurenkov, N V Latysheva, M V Naprienko, O R Orlova, E G Filatova, V S Shevchenko, P N Yakovleva
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引用次数: 1

Abstract

Objective: To access the efficacy and safety of the first Russian botulinum toxin type A (Relatox) as a headache prophylaxis in adult with chronic migraine (CM).

Material and methods: The randomized, one-blind, multicenter, active-controlled, parallel-group trial study involved 209 patients with CM aged from 19 to 65 years. The patients were randomized to injections of the Russian botulinum toxin type A - Relatox (n=101) or onabotulinumtoxinA injections - Botox (n=108). The duration of the study was 16 weeks, which included five visits of patients every 4 weeks. Relatox and Botox were injected once into seven muscle groups of the head and neck at a dose of 155-195 units. Primary efficacy variable was mean change from baseline in frequency of headache days after 12 weeks. Secondary efficacy variables were mean changes from the baseline to week 12 in frequency of migraine days, acute headache pain medication intakes days; headache intensity; proportion of patients achieving ≥50% reduction from baseline in headache days, the proportion of the patients with medication overuse, the proportion of the patients with severe (≥60) Headache Impact Test-6 score and with a severe (≥21) MIDAS score.

Results: Analyses demonstrated a large mean decrease from baseline in frequency of headache days, without statistically significant between-group differences Relatox vs Botox at week 12 (-10.89 vs -10.06; p=0.365) and at other time points. Significant differences from baseline were also observed for all secondary efficacy variables at all time points without differences between the groups. The proportion of patients achieving ≥50% reduction from baseline in headache days was 75.0% and 70% in the Relatox and Botox groups, respectively (OR, CI 95% 1.58 [0.84; 3.02], p=0.155). Adverse events (AE) occurred in 15.8% of Relatox patients and 15.7% of Botox patients (p=1.000). No unexpected AE were identified.

Conclusion: The results demonstrate that the first Russian botulinum toxin type A (Relatox) is an effective prophylactic treatment for CM in adult patients. Relatox led to significant improvements from baseline in multiple measures of headache symptoms, headache-related disability and quality of life. For the first time, a comparative analysis of two botulinum toxin type A products in parallel groups showed no less (not inferior) efficacy and safety of Relatox relative to Botox in the treatment of CM in adults.

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[A型肉毒毒素(Relatox)治疗成人慢性偏头痛:IIIb期随机、单盲、多中心、主动对照、平行组试验结果]。
目的:探讨俄罗斯第一种A型肉毒毒素(Relatox)预防成人慢性偏头痛(CM)头痛的疗效和安全性。材料与方法:随机、单盲、多中心、主动对照、平行组试验研究纳入209例CM患者,年龄19 ~ 65岁。患者被随机分为注射俄罗斯A型肉毒杆菌毒素(101例)和单肉毒杆菌毒素(108例)两组。研究的持续时间为16周,其中包括每4周对患者进行5次访问。Relatox和Botox分别以155-195单位的剂量注射到头颈部的7个肌肉群中。主要疗效变量为12周后头痛天数频率较基线的平均变化。次要疗效变量为从基线到第12周偏头痛天数频率、急性头痛药物摄入天数的平均变化;头痛强度;头痛天数较基线减少≥50%的患者比例、药物过度使用患者比例、严重(≥60)头痛影响测试-6评分和严重(≥21)MIDAS评分患者比例。结果:分析显示头痛天数的频率比基线有很大的平均下降,在第12周时,Relatox和Botox组间差异无统计学意义(-10.89 vs -10.06;P =0.365)和其他时间点。在所有时间点,所有次要疗效变量也观察到与基线的显著差异,组间无差异。在Relatox组和肉毒杆菌素组中,头痛天数比基线减少≥50%的患者比例分别为75.0%和70% (OR, CI 95% 1.58 [0.84;3.02, p = 0.155)。15.8%的Relatox患者和15.7%的Botox患者发生了不良事件(AE) (p=1.000)。未发现意外AE。结论:第一俄A型肉毒毒素(Relatox)是预防成人CM的有效药物。Relatox使头痛症状、头痛相关残疾和生活质量的多项指标从基线显著改善。两种a型肉毒杆菌毒素产品在平行组中的比较分析首次显示,相对于肉毒杆菌素,Relatox在治疗成人CM中的疗效和安全性并不逊色(并不逊色)。
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Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova Medicine-Psychiatry and Mental Health
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