从另一种靶向 CGRP 通路的 mAb 转用 fremanezumab 对偏头痛患者的实际疗效。

IF 2.7 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Dental and Medical Problems Pub Date : 2024-01-01 DOI:10.17219/dmp/174706
Marta Waliszewska-Prosół, Paolo Martelletti
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引用次数: 0

摘要

本文是题为 "fremanezumab 对从另一种靶向 CGRP 通路的 mAb 转用的偏头痛患者的实际疗效:Finesse 研究的亚组分析 "的研究文章摘要:降钙素基因相关肽(CGRP)作为偏头痛治疗靶点的发现是近年来神经学领域最伟大的成就之一。针对 CGRP 的特异性抗体通过受体(erenumab)或配体(fremanezumab、galcanezumab、eptinezumab)与 CGRP 结合。单克隆抗体(mAbs)是一种有效、安全且耐受性良好的药物,已被批准用于每月至少4天偏头痛的预防性治疗。然而,在临床实践中,也观察到了使用 mAbs 治疗失败的案例,因此就产生了一个问题:是否值得使用具有不同作用机制的抗体进行治疗?Finesse 研究旨在评估 fremanezumab 对曾使用其他抗 CGRP 通路 mAbs 治疗失败患者的疗效。在153名曾使用mAb失败的患者中,改用fremanezumab后,42.8%的患者每月偏头痛天数减少了≥50%。该结论强调,对于既往治疗失败的患者,应考虑改用另一种抗体。
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Real-world effectiveness of fremanezumab in patients with migraine switching from another mAb targeting the CGRP pathway.

This is a summary of the research article entitled "Real-world effectiveness of fremanezumab in patients with migraine switching from another mAb targeting the CGRP pathway: A subgroup analysis of the Finesse Study".The discovery of calcitonin gene-related peptide (CGRP) as a therapeutic target in migraine has been one of the greatest achievements in neurology in recent years. Specific antibodies against CGRP bind to it either via a receptor (erenumab) or ligand (fremanezumab, galcanezumab, eptinezumab). Monoclonal antibodies (mAbs) are effective, safe and welltolerated drugs that have been approved for prophylactic treatment if there are at least 4 days with migraine per month. However, in clinical practice, the failure of treatment with mAbs has been observed, and thus the question arises whether it is worthwhile to include treatment using an antibody with a different mechanism of action.The Finesse Study was designed to evaluate the efficacy of fremanezumab in patients with a history of prior treatment failure with other mAbs against the CGRP pathway. Among the 153 patients with priorly failed mAbs, switching to fremanezumab led to a ≥50% reduction in the number of days with migraine per month in 42.8% of patients. The conclusion emphasizes that switching to another antibody should be considered in patients with prior therapy failure.

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来源期刊
CiteScore
4.00
自引率
3.80%
发文量
58
审稿时长
53 weeks
期刊最新文献
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