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首页> 外文期刊>Frontiers in Neuropharmacology >Calcitonin Gene-Related Peptide Monoclonal Antibodies Versus Botulinum Neurotoxin a in the Preventive Treatment of Chronic Migraine: An Adjusted Indirect Treatment Comparison Meta-Analysis
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Calcitonin Gene-Related Peptide Monoclonal Antibodies Versus Botulinum Neurotoxin a in the Preventive Treatment of Chronic Migraine: An Adjusted Indirect Treatment Comparison Meta-Analysis

机译:Calcitonin基因相关的肽单克隆抗体对肉毒杆菌神经毒素A中的预防治疗慢性偏头痛:调整后的间接治疗比较荟萃分析

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Calcitonin gene-related peptide monoclonal antibodies (CGRPmAbs) are new agents approved by the US Food and Drug Administration for preventive treatment of chronic migraine. Comparison between CGRPmAbs and previously approved Botulinum neurotoxin A (BoNT-A) will inform optimal preventive treatment of chronic migraine, but head-to-head trials are lacking. We therefore aimed to perform adjusted indirect comparison between CGRPmAbs and BoNT-A through a meta-analysis. Methods: OVID MEDLINE, EMBASE and the Cochrane central register of controlled trials, clinical registries, and government websites were searched from inception to September 2019. Randomized controlled trials comparing CGRPmAbs or BoNT-A with placebo in the preventive treatment of chronic migraine were included. The primary outcomes were headache days and migraine days measured at week 12. Data were synthesized by using a frequentist approach; and the treatments were ranked by P-score. Results: We included 10 trials (n = 4,678) after screening 1049 candidates. Six trials were with low risk of bias. Fremanezumab had an effect similar to BoNT-A in the reduction of headache days at week 12 (standard mean difference [SMD] 0.08, 95%CI -0.55 to -0.7). Galcanezumab reduced more migraine days than BoNT-A at week 12 (SMD, -0.94, 95% CI ?1.24 to ?0.63); fremanezumab showed similar findings (SMD, ?0.55, 95%CI ?0.85 to ?0.24). Galcanezumab and fremanezumab had better effect in mitigating headache impact at week 12. CGRPmAbs and BoNT-A had similar adverse event rate. Conclusion: CGRPmAbs and BoNT-A had similar effect in the preventive treatment of chronic migraine. BoNT-A might be preferentially selected owing to its cost-effectiveness profiles. Further studies with direct comparison of the two treatments are warranted.
机译:Calcitonin基因相关的肽单克隆抗体(CGRPMABs)是美国食品和药物管理局批准的新试剂,用于预防慢性偏头痛。 CGRPMABs与先前批准的肉毒杆菌神经毒素A(Bont-A)的比较将为慢性偏头痛提供最佳的预防治疗,但缺乏头脑前往头试验。因此,我们旨在通过META分析进行CGRPMABS和BONT-A之间的调整后的间接比较。方法:从2009年9月开始搜查了对受控试验,临床登记和政府网站的Ovid Medline,Embase和Cochrane Centralite,包括在慢性偏头痛预防治疗中,将CGRPMABS或Bont-A与安慰剂进行比较的随机对照试验。主要结果是头痛日,第12周测量的偏头发日。通过使用频繁的方法来合成数据;并且治疗被P级排名。结果:在筛选1049名候选人后,我们包括10项试验(n = 4,678)。六项试验具有低风险的偏见。 Fremanezumab在第12周(标准平均值差异[SMD] 0.08,95%CI -0.55至-0.7)中,Fremanezumab的效果类似于笨蛋Galcanezumab在第12周(SMD,-0.94,95%CI-1.24至0.63); Fremanezumab显示出类似的发现(SMD,?0.55,95%CI?0.85至0.24)。 Galcanezumab和Fremanezumab在第12周的减轻头痛影响方面具有更好的影响.CGRPMABS和Bont-A具有类似的不良事件率。结论:CGRPMABS和逆向-A在慢性偏头痛的预防治疗中具有相似的效果。由于其成本效益配置文件,可能优先选择Bont-A。有必要进一步研究两种治疗方法。

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