Placebo response with subcutaneous injections in calcitonin gene-related peptide receptor monoclonal antibody migraine preventative trials – A systematic review and meta-analysis

Q3 Medicine
S. Gorantla, Murali Mohan Reddy Gopireddy, Archana Bhat, Lavanya Ayyasamy, Sarath Kumar Jaganathan Jaishankar, Bassil Kherallah, H. Nersesyan
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引用次数: 1

Abstract

Background: The majority of CGRP monoclonal antibodies for migraine prevention are administered subcutaneously. Therefore, we attempted to calculate the pooled placebo response with subcutaneous placebo injections in this systematic review and meta-analysis. Methods: We identified 16 randomized controlled trials that met our inclusion and exclusion criteria through a comprehensive search in five electronic databases (PubMed Central, EMBASE, MEDLINE, Cochrane library and clinicaltrials.gov). The risk of bias was assessed for all included studies. Random effects model was used to calculate pooled mean monthly migraine days and 50% response rates. Results: A total of 4240 subjects were included from 16 studies in this meta-analysis. The pooled mean monthly migraine day reduction with subcutaneous placebo injections was 2.15 (95% CI: 1.60–2.69). The pooled proportion of patients achieving a 50% reduction in mean monthly headache days was 26% (95% CI: 20%–31%). Placebo response accounted for more than 50% of therapeutic gain in our study. Conclusion: A substantial placebo response was noted with subcutaneous injections in migraine CGRP monoclonal antibody clinical trials. This meta-analysis may serve as a reference point to calculate sample size in clinical trials using subcutaneous interventions for migraine prevention. We registered our study at PROSPERO (CRD42020185300).
降钙素基因相关肽受体单克隆抗体偏头痛预防试验中皮下注射安慰剂的反应——系统综述和荟萃分析
背景:大多数用于预防偏头痛的CGRP单克隆抗体都是皮下注射的。因此,在本系统综述和荟萃分析中,我们试图计算皮下注射安慰剂的合并安慰剂反应。方法:我们通过在五个电子数据库(PubMed Central、EMBASE、MEDLINE、Cochrane library和clinicaltrials.gov)中进行全面搜索,确定了16项符合纳入和排除标准的随机对照试验。评估了所有纳入研究的偏倚风险。随机效应模型用于计算合并的每月平均偏头痛天数和50%的缓解率。结果:本荟萃分析共纳入16项研究中的4240名受试者。皮下注射安慰剂后每月平均偏头痛天数减少2.15天(95%置信区间:1.60–2.69)。每月平均头痛天数减少50%的患者比例为26%(95%可信区间:20%–31%)。在我们的研究中,安慰剂反应占治疗增益的50%以上。结论:在偏头痛CGRP单克隆抗体临床试验中,皮下注射有显著的安慰剂反应。这项荟萃分析可以作为在使用皮下干预预防偏头痛的临床试验中计算样本量的参考点。我们在PROSPERO注册了我们的研究(CRD42020185300)。
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
Cephalalgia Reports
Cephalalgia Reports Medicine-Neurology (clinical)
CiteScore
2.50
自引率
0.00%
发文量
17
审稿时长
9 weeks
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