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偏头痛预防中CGRP靶向药物的开放标签试验:一项叙述性综述。

Open-label trials for CGRP-targeted drugs in migraine prevention: A narrative review.

作者信息

Raffaelli Bianca, De Icco Roberto, Corrado Michele, Terhart Maria, Ailani Jessica

机构信息

Department of Neurology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Clinician Scientist Program, Berlin Institute of Health, Berlin, Germany.

出版信息

Cephalalgia. 2023 Feb;43(2):3331024221137091. doi: 10.1177/03331024221137091.

Abstract

BACKGROUND

Calcitonin gene-related peptide-targeted drugs have proven safe and effective for migraine prevention in large randomized-controlled, double-blind trials with an average duration of six months. Open-label studies may provide additional information on the long-term safety and efficacy of these substances.

METHODS

We searched PubMed for open-label trials with calcitonin gene-related peptide(-receptor) monoclonal antibodies and calcitonin gene-related peptide-receptor antagonists. We summarized and critically analyzed the literature in a narrative way.

RESULTS

Overall, 13 open-label trials were included in this review (n = 4 for erenumab, n = 4 for galcanezumab, n = 3 for fremanezumab, n = 1 for eptinezumab, n = 1 for atogepant). Open-label trial duration ranged between 12 and 264 weeks. No safety concerns emerged, and the adverse events profile was similar to the double-blind study phase. Discontinuation rates were generally low with >75% of patients remaining in the trials after one year. Efficacy data showed a sustained reduction of migraine frequency throughout the trials, along with a lasting improvement in quality of life.

CONCLUSIONS

The open-label study program for calcitonin gene-related peptide-targeted migraine preventives confirms the favorable safety and efficacy profile of these drugs over time. Treatment adherence appears higher than with previous unspecific migraine preventives. Real-world data and post-marketing surveillance studies may corroborate and complement open-label results.

摘要

背景

在平均为期6个月的大型随机对照双盲试验中,降钙素基因相关肽靶向药物已被证明对预防偏头痛安全有效。开放标签研究可能会提供有关这些物质长期安全性和有效性的更多信息。

方法

我们在PubMed上搜索了有关降钙素基因相关肽(-受体)单克隆抗体和降钙素基因相关肽受体拮抗剂的开放标签试验。我们以叙述方式总结并批判性地分析了文献。

结果

总体而言,本综述纳入了13项开放标签试验(erenumab为4项,galcanezumab为4项,fremanezumab为3项,eptinezumab为1项,atogepant为1项)。开放标签试验持续时间在12至264周之间。未出现安全问题,不良事件情况与双盲研究阶段相似。停药率普遍较低,一年后超过75%的患者仍留在试验中。疗效数据显示,在整个试验过程中偏头痛发作频率持续降低,生活质量持续改善。

结论

降钙素基因相关肽靶向偏头痛预防药物的开放标签研究计划证实了这些药物长期良好的安全性和有效性。治疗依从性似乎高于以往非特异性偏头痛预防药物。真实世界数据和上市后监测研究可能会证实并补充开放标签研究结果。

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