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依瑞奈玛(AMG334)治疗既往预防治疗失败的慢性偏头痛患者的疗效和安全性:一项随机、双盲、安慰剂对照研究的亚组分析。

Efficacy and safety of erenumab (AMG334) in chronic migraine patients with prior preventive treatment failure: A subgroup analysis of a randomized, double-blind, placebo-controlled study.

机构信息

1 Danish Headache Center and Department of Neurology, Rigshospitalet Glostrup, Faculty of Medical and Health Sciences, University of Copenhagen, Copenhagen, Denmark.

2 Geisel School of Medicine at Dartmouth, Hanover, NH, USA.

出版信息

Cephalalgia. 2018 Sep;38(10):1611-1621. doi: 10.1177/0333102418788347. Epub 2018 Jul 8.

Abstract

Background Erenumab was effective and well tolerated in a pivotal clinical trial of chronic migraine. Here, we evaluated efficacy and safety of monthly erenumab (70 mg or 140 mg) versus placebo in the subgroup of patients who had previously failed preventive treatment(s) (≥ 1, ≥ 2 prior failed medication categories) and in patients who had never failed. Methods Subgroup analyses evaluated change from baseline in monthly migraine days; achievement of ≥ 50% and ≥ 75% reduction in monthly migraine days; and change in monthly acute migraine-specific medication days. Adverse events were evaluated for each subgroup. Results Treatment with both doses of erenumab resulted in greater reductions in monthly migraine days (primary endpoint) at Month 3 (treatment difference [95% CI], never failed subgroup: -2.2 [-4.1, -0.3] for 70 mg and -0.5 [-2.4, 1.5] for 140 mg; ≥ 1 prior failed medication categories subgroup: -2.5 [-3.8, -1.2], for 70 mg and -3.3 [-4.6, -2.1] for 140 mg; ≥ 2 prior failed medication categories subgroup: -2.7 [-4.2, -1.2], for 70 mg and -4.3 [-5.8, -2.8] for 140 mg). Similar results were observed in the monthly acute migraine-specific medication days endpoint, and in the achievement of ≥ 50% and ≥ 75% reduction in monthly migraine days. There were no new or unexpected safety issues. Conclusion Erenumab showed consistent efficacy in chronic migraine patients who had failed prior preventive treatments and was well tolerated across subgroups.

摘要

背景

依瑞奈umab 在慢性偏头痛的关键临床试验中有效且耐受性良好。在此,我们评估了每月依瑞奈umab(70mg 或 140mg)与安慰剂在先前预防治疗失败(≥1 种、≥2 种先前失败的药物类别)的亚组患者和从未失败的患者中的疗效和安全性。

方法

亚组分析评估了每月偏头痛天数从基线的变化;达到每月偏头痛天数减少≥50%和≥75%;以及每月急性偏头痛特异性药物天数的变化。评估了每个亚组的不良事件。

结果

两种剂量的依瑞奈umab 在第 3 个月时均导致每月偏头痛天数(主要终点)更大幅度的减少(从未失败的亚组:70mg 为-2.2[-4.1,-0.3],140mg 为-0.5[-2.4,1.5];≥1 种先前失败的药物类别的亚组:70mg 为-2.5[-3.8,-1.2],140mg 为-3.3[-4.6,-2.1];≥2 种先前失败的药物类别的亚组:70mg 为-2.7[-4.2,-1.2],140mg 为-4.3[-5.8,-2.8])。在每月急性偏头痛特异性药物天数终点以及达到每月偏头痛天数减少≥50%和≥75%方面也观察到了类似的结果。没有新的或意外的安全性问题。

结论

依瑞奈umab 在先前预防治疗失败的慢性偏头痛患者中显示出一致的疗效,且在各亚组中具有良好的耐受性。

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