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Efficacy and Safety of Monoclonal Antibody Against Calcitonin Gene-Related Peptide or Its Receptor for Migraine: A Systematic Review and Network Meta-analysis

机译:单克隆抗体对Calcitonin基因相关肽或其对偏头痛受体的功效和安全性:系统审查和网络Meta分析

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The optimal monoclonal antibody against calcitonin gene-related peptide (CGRP) for adult patients with migraine has yet to be determined. Therefore, we aimed to compare the effectiveness of different monoclonal antibodies against CGRP or its receptor for adult patients with migraine through a network meta-analysis of randomized controlled trials. Methods: We systematically searched the MEDILNE, Embase, ClinicalTrials.gov, and Cochrane Library databases for relevant publications from inception until October 30, 2020. Only randomized clinical trials of adults with migraine that assessed any calcitonin gene-related peptide monoclonal antibody and reported clinical outcomes were included. The primary outcomes were changes in monthly migraine days and treatment-emergent adverse events Results: We initially retrieved 2,070 publications, and ultimately, 18 randomized clinical trials totaling 8,926 patients were included. In terms of efficacy, eptinezumab (MD ?1.43, 95% CrI ?2.59 to ?0.36), erenumab (MD ?1.61, 95% CrI ?2.40 to ?0.84), fremanezumab (MD ?2.19, 95% CrI ?3.15 to ?1.25), and galcanezumab (MD ?2.10, 95% CrI ?2.76 to ?1.45) significantly reduced MMDs compared with placebo. In terms of safety, only galcanezumab increased the incidences of TEAEs (RR 1.11, 95% CrI 1.01–1.22) and serious adverse events (RR 2.95, 95% CrI 1.41–6.87) compared with placebo. Conclusion: Most drugs performed similarly and were superior to placebo in most of our analyses. Further head-to-head research on different types of CGRP monoclonal antibodies is necessary to validate the present findings.
机译:尚未确定对成年患者的患有成年患者的降钙素基因相关肽(CGRP)的最佳单克隆抗体。因此,我们旨在通过网络荟萃分析对成年患者对成年患者的不同单克隆抗体对CGRP或其受体的有效性进行比较随机对照试验的网络荟萃分析。方法:我们系统地搜索了Medilne,Embase,Clinicaltrials.gov和Cochrane图书馆数据库,以实现相关出版物,直到2020年10月30日期。只有偏头痛的成年人随机临床试验,评估任何Calcitonin基因相关的肽单克隆抗体并报告临床包括结果。主要结果是每月偏头发日的变化和治疗紧急的不良事件结果:我们最初检索了2,070个出版物,最终,18例随机临床试验总计8,926名患者。在疗效方面,EPTinezumab(MD?1.43,95%CRI?2.59至0.36),Erenumab(MD?1.61,95%CRI?2.40至?0.84),Fremanezumab(MD?2.19,95%CRI?3.15到? 1.25)和Galcanezumab(MD?2.10,95%CRI?2.76至?1.45)与安慰剂相比,MMDS显着降低。就安全性而言,只有加元的茶叶(RR 1.11,95%CRI 1.01-1.22)增加了Galcanezumab(RR 1.11,95%CRI 1.01-1.22)和严重不良事件(RR 2.95,95%CRI 1.41-6.87)。结论:大多数药物表现出类似,在大多数分析中都有优于安慰剂。对不同类型的CGRP单克隆抗体进行进一步的头脑研究是为了验证当前研究结果。

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