Efficacy and Safety of Fremanezumab in Patients with Migraine: Real-World Evidence in a Private Neurological Center

Q4 Medicine
Marli Vitorino
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Abstract

Introduction: Migraine is the first cause of disability under 50 years of age. In the last decade there were significant advances in the comprehension of this disorder that led to the development of specific treatments, such as those targeting calcitonin gene-related peptide (CGRP) or its receptor including monoclonal antibodies. Here, we present real life results of a cohort of migraine patients treated with fremanezumab. Material and Methods: We analysed data, collected prospectively for 18 months, of consecutive patients with migraine treated with fremanezumab in a Lisbon center. Patients had a baseline evaluation and monthly visits. Data included monthly headache days, a composite headache measure (days x pain intensity), acute treatment intake and adverse events. Patients also fulfilled quality of life and migraine impact scales at 1st, 3rd, 6th, 9th and 12th months of treatment and were evaluated after treatment withdrawal. Efficacy was defined as a reduction ≥ 30% or ≥ 50% of the number of monthly headache days (in chronic and episodic migraine, respectively) compared to baseline. Results: We included 29 patients (47.8 years of age, 25 female) with chronic (n=20) or high frequency episodic (n=9), migraine previously resistant to an average of 3.3 oral preventives/botulinum toxin, 20 with medication overuse. Efficacy increased from 62% in the 1st month to 76.9% on the 3rd and there was a significant reduction of migraine headache days, acute medication intake, index and HIT-6 scores and improved quality of life in all assessment periods compared to baseline. The most common adverse events were constipation (27.6%) and pain on the injection site (20.7%) leading to interruption of treatment in one patient. There was no increase in the number of headache days or acute medication intake five months after treatment interruption. Conclusion: These results corroborate data from clinical trials about the efficacy and safety of fremanezumab, showing an improvement of different migraine measures and impact, even in patients with resistant migraine and medication overuse. In general, adverse events were well tolerated not leading to treatment withdrawal.
Fremanezumab在偏头痛患者中的疗效和安全性:私人神经学中心的真实世界证据
引言:偏头痛是50岁以下残疾的首要原因。在过去的十年里,对这种疾病的理解取得了重大进展,这导致了特异性治疗的发展,例如针对降钙素基因相关肽(CGRP)或其受体(包括单克隆抗体)的治疗。在这里,我们展示了一组接受氟曼珠单抗治疗的偏头痛患者的真实生活结果。材料和方法:我们分析了在里斯本一家中心接受氟曼珠单抗治疗的连续偏头痛患者的前瞻性收集的18个月的数据。患者进行了基线评估和每月就诊。数据包括每月头痛天数、综合头痛测量(天数x疼痛强度)、急性治疗摄入量和不良事件。患者在治疗的第1、3、6、9和12个月也达到了生活质量和偏头痛影响量表,并在停药后进行了评估。疗效定义为与基线相比,每月头痛天数(分别为慢性偏头痛和发作性偏头痛)减少≥30%或≥50%。结果:我们纳入了29名患有慢性(n=20)或高频发作性(n=9)偏头痛的患者(47.8岁,25名女性),这些患者之前平均对3.3种口服预防药物/肉毒杆菌毒素有耐药性,20名患者过度用药。疗效从第一个月的62%增加到第三个月的76.9%,与基线相比,偏头痛天数、急性药物摄入、指数和HIT-6评分显著减少,生活质量也有所改善。最常见的不良事件是便秘(27.6%)和注射部位疼痛(20.7%),导致一名患者的治疗中断。治疗中断五个月后,头痛天数或急性药物摄入没有增加。结论:这些结果证实了关于氟曼珠单抗疗效和安全性的临床试验数据,表明不同的偏头痛措施和影响都有所改善,即使是在顽固性偏头痛和药物过度使用的患者中也是如此。一般来说,不良事件耐受性良好,不会导致停药。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Sinapse
Sinapse Medicine-Neurology (clinical)
CiteScore
0.10
自引率
0.00%
发文量
26
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