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加卡尼单抗用于丛集性头痛预防性治疗的疗效和安全性:一项系统评价和荟萃分析。

Efficacy and safety of galcanezumab for cluster headache preventive treatment: a systematic review and meta-analysis.

作者信息

Barbosa da Silva Marina, Baroni Coelho de Oliveira Ferreira Domênica, Mendieta Cristian D, Pereira da Silva Hamilcar, Aguiar Nogueira-Rosa Lívia, Moraes-Figueiredo Nathalia

机构信息

Universidade Barão de Mauá, São Paulo, Brazil.

Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

Neurol Res. 2025 Jan;47(1):63-76. doi: 10.1080/01616412.2024.2440022. Epub 2024 Dec 17.

Abstract

BACKGROUND

Galcanezumab is a monoclonal antibody targeting the CGRP pathway and represents the latest disease-specific and mechanism-based therapeutic option for cluster headache (CH).

OBJECTIVE

We performed a systematic review and meta-analysis to evaluate the efficacy and safety of galcanezumab for CH.

METHODS

We searched PubMed, Embase, and Cochrane Library for studies implementing galcanezumab for episodic and chronic CH. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and Reporting Guidelines for Meta-analyses of Observational Studies (MOOSE) guidelines. The primary outcome was efficacy, defined by a reduction from the baseline of at least 50% in the weekly frequency of CH attacks and the Patient Global Impression of Improvement scale (PGI-I). Secondary outcomes included treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs).

RESULTS

A total of 504 patients were included from 6 studies, of which 2 were RCTs. The follow-up period ranged from 3 weeks to 15 months. The mean age was 44.4 ± 10.2 years, with 24.4% female patients. Overall efficacy was 76.0% (95% CI 0.67-0.85), TEAEs were observed in 48.0% of patients (95% CI 0.25-0.72), and the most common were nasopharyngitis, local injection pain, and local injection swelling. TEAEs were, however, considerably higher within the 300 mg dose group compared with the 240 mg dose group, 80.0% (95% CI 0.65-0.87) versus 28.0% (95% CI 0.12-0.47), respectively.

CONCLUSION

This meta-analysis suggests that galcanezumab is effective in reducing the number of CH attacks and can be considered a safe medication.

摘要

背景

加卡尼单抗是一种靶向降钙素基因相关肽(CGRP)途径的单克隆抗体,是丛集性头痛(CH)最新的针对疾病和基于发病机制的治疗选择。

目的

我们进行了一项系统评价和荟萃分析,以评估加卡尼单抗治疗CH的疗效和安全性。

方法

我们检索了PubMed、Embase和Cochrane图书馆,查找使用加卡尼单抗治疗发作性和慢性CH的研究。我们遵循系统评价和荟萃分析的首选报告项目(PRISMA)以及观察性研究荟萃分析报告指南(MOOSE)。主要结局是疗效,定义为CH发作的每周频率和患者总体改善印象量表(PGI-I)较基线降低至少50%。次要结局包括治疗中出现的不良事件(TEAE)和严重不良事件(SAE)。

结果

6项研究共纳入504例患者,其中2项为随机对照试验。随访期为3周-15个月。平均年龄为44.4±10.2岁,女性患者占24.4%。总体疗效为76.0%(95%CI 0.67-0.85),48.0%的患者观察到TEAE(95%CI 0.25-0.72),最常见的是鼻咽炎、局部注射疼痛和局部注射肿胀。然而,300mg剂量组的TEAE明显高于240mg剂量组,分别为80.0%(95%CI 0.65-0.87)和28.0%(95%CI 0.12-0.47)。

结论

这项荟萃分析表明,加卡尼单抗可有效减少CH发作次数,可被认为是一种安全的药物。

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