Estimating Changes in Clinical Outcomes after Discontinuation of Anti-CGRP Targeting Therapy for Migraine Prophylaxis: A Systematic Review and Meta-analysis.

IF 7.4 2区 医学 Q1 CLINICAL NEUROLOGY
Luana Miyahira Makita, Thales Pardini Fagundes, Pedro Henrique Reginato, Lucca Passow Carpinelli, Giovanna de Freitas Morais, Renata Trinkel Montanarin, Rafael de Freitas Kleimmann, Rafael Eduardo Streit, Aishwarya Koppanatham, Andressa Christine Sales Rodrigues, Elcio Juliato Piovesan
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引用次数: 0

Abstract

Background and objectives: Anti-calcitonin gene-related peptide (CGRP) therapies have significantly improved migraine prevention, but the long-term impact of discontinuation remains unclear. This systematic review and meta-analysis aimed to evaluate clinical outcomes following the cessation of anti-CGRP therapy.

Methods: PubMed, Embase, and Cochrane databases were searched up to September 2024 for randomized or observational studies reporting post-discontinuation effects in patients with episodic or chronic migraine who had been preventively treated with anti-CGRP monoclonal antibodies or gepants. The primary outcome was the mean change in monthly migraine days from baseline to post-discontinuation. Secondary outcomes included acute headache medication use, the mean change in migraine frequency from active therapy to treatment cessation, and ≥ 50% responder rates. Heterogeneity was assessed with prediction intervals (PIs) for binary outcomes and I2 statistics for continuous data. Random-effects models pooled mean differences (MDs) and risk ratios (RRs), with subgroup analyses based on follow-up duration, study design, and individuals with chronic migraine.

Results: Eight studies (n = 1012) evaluating anti-CGRP monoclonal antibodies interruption were included. No studies on gepant cessation were found. Monthly migraine days decreased significantly post-discontinuation compared with baseline (MD -3.78; 95% CI -4.89, -2.67; I2 = 57%; p < 0.05), with reductions of - 5.70 days at 1 month and - 3.62 days at 3 months. Patients with chronic migraine showed sustained reductions (MD - 6.54; 95% CI - 8.64, - 4.43; I2 = 68%; p < 0.05) in the days per month with migraine between cessation and pre-treatment periods. Monthly acute headache medication days declined from baseline (MD - 1.74; 95% CI - 2.84, - 0.64; I2 = 0%; p < 0.05). Monthly migraine days increased at 3 months after discontinuation compared with just before discontinuation (MD 4.43; 95% CI 2.61, 6.25; I2 = 86%; p < 0.05), with monthly acute headache drug usage rising by 3.22 days. Responder rates of ≥ 50% declined (RR 0.42; 95% CI 0.33, 0.53; PI 0.17, 1.03; p < 0.05).

Conclusions: Migraine burden worsened after discontinuation of anti-CGRP targeting therapies but remained lower than pretreatment levels. Further research is needed to explore disease-modifying potential and optimal discontinuation strategies. PROSPERO registration number CRD42024595771.

估计停止抗cgrp靶向治疗偏头痛后临床结果的变化:一项系统回顾和荟萃分析。
背景和目的:抗降钙素基因相关肽(CGRP)治疗可以显著改善偏头痛的预防,但停止治疗的长期影响尚不清楚。本系统综述和荟萃分析旨在评估停止抗cgrp治疗后的临床结果。方法:检索PubMed、Embase和Cochrane数据库,检索截至2024年9月的随机或观察性研究,这些研究报告了服用抗cgrp单克隆抗体或抗cgrp单克隆抗体预防性治疗的发作性或慢性偏头痛患者停药后的疗效。主要结局是每月偏头痛天数从基线到停药后的平均变化。次要结局包括急性头痛药物的使用,偏头痛频率从积极治疗到停止治疗的平均变化,以及≥50%的应答率。采用预测区间(pi)对二元结果进行评估,I2统计对连续数据进行评估。随机效应模型汇集了平均差异(MDs)和风险比(rr),并根据随访时间、研究设计和慢性偏头痛患者进行了亚组分析。结果:纳入8项评估抗cgrp单克隆抗体中断的研究(n = 1012)。没有关于妊娠停止的研究被发现。与基线相比,停药后每月偏头痛天数显著减少(MD -3.78; 95% CI -4.89, -2.67; I2 = 57%; p < 0.05), 1个月减少- 5.70天,3个月减少- 3.62天。慢性偏头痛患者在停止治疗和治疗前期间每月偏头痛天数持续减少(MD - 6.54; 95% CI - 8.64, - 4.43; I2 = 68%; p < 0.05)。每月急性头痛用药天数较基线下降(MD - 1.74; 95% CI - 2.84, - 0.64; I2 = 0%; p < 0.05)。与停药前相比,停药后3个月每月偏头痛天数增加(MD 4.43; 95% CI 2.61, 6.25; I2 = 86%; p < 0.05),每月急性头痛药物使用量增加3.22天。≥50%的应答率下降(RR 0.42; 95% CI 0.33, 0.53; PI 0.17, 1.03; p < 0.05)。结论:停止抗cgrp靶向治疗后偏头痛负担加重,但仍低于治疗前水平。需要进一步的研究来探索改善疾病的潜力和最佳的停药策略。普洛斯彼罗注册号CRD42024595771。
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来源期刊
CNS drugs
CNS drugs 医学-精神病学
CiteScore
12.00
自引率
3.30%
发文量
82
审稿时长
6-12 weeks
期刊介绍: CNS Drugs promotes rational pharmacotherapy within the disciplines of clinical psychiatry and neurology. The Journal includes: - Overviews of contentious or emerging issues. - Comprehensive narrative reviews that provide an authoritative source of information on pharmacological approaches to managing neurological and psychiatric illnesses. - Systematic reviews that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. - Adis Drug Reviews of the properties and place in therapy of both newer and established drugs in neurology and psychiatry. - Original research articles reporting the results of well-designed studies with a strong link to clinical practice, such as clinical pharmacodynamic and pharmacokinetic studies, clinical trials, meta-analyses, outcomes research, and pharmacoeconomic and pharmacoepidemiological studies. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in CNS Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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