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2型哮喘中的单克隆抗体:一项更新的网状Meta分析。

Monoclonal antibodies in type 2 asthma: an updated network meta-analysis.

作者信息

Edris Ahmed, Lahousse Lies

机构信息

Pharmaceutical Care Unit, Department of Bioanalysis, Ghent University, Ghent, Belgium.

Pharmaceutical Care Unit, Department of Bioanalysis, Ghent University, Ghent, Belgium -

出版信息

Minerva Med. 2021 Oct;112(5):573-581. doi: 10.23736/S0026-4806.21.07623-0. Epub 2021 May 14.

Abstract

INTRODUCTION

Novel treatments target eosinophilic inflammation in type 2 asthma. We aimed to evaluate and meta-analyze the efficacy of monoclonal antibodies to reduce exacerbation rate.

EVIDENCE ACQUISITION

PubMed and Embase were searched for phase II and phase III randomized clinical trials with monoclonal antibodies targeting key mediators of type 2-associated asthma between 2019 and 2021 to update our previous meta-analysis covering studies published from 2005 to 2018. Five-hundred and sixty six publications have been identified, of which six recent trials (on top of 30 previously identified) involving mepolizumab, benralizumab, reslizumab and dupilumab met our inclusion criteria. As no head-to-head trials were retrieved from literature, we performed an arm-based network meta-analysis including a total of 19 RCTs to compare effects on exacerbation rate between the different treatments.

EVIDENCE SYNTHESIS

Benralizumab significantly reduced the risk of exacerbations compared to the pooled placebo in our network meta-analysis (median effect difference: -0.520, 95% CI [-1.010- -0.048]). No biologic showed superiority over the others in indirect comparisons. Large reductions in exacerbation rates were observed compared to placebo, though only benralizumab was sufficiently powered (N.=2564) to demonstrate significantly decreased exacerbation rates both in the overall population and in the subgroup analysis of IL-5 acting agents compared to placebo.

CONCLUSIONS

Monoclonal antibodies have proven their benefit to reduce exacerbation rates in severe persistent eosinophilic asthma in the published trials. No biological showed superiority over the others emphasizing the need for clearly defined endotypes indicating those patients who will optimally benefit for each treatment.

摘要

引言

新型疗法针对2型哮喘中的嗜酸性粒细胞炎症。我们旨在评估和荟萃分析单克隆抗体降低急性加重率的疗效。

证据获取

检索了PubMed和Embase数据库,以查找2019年至2021年间针对2型相关哮喘关键介质的单克隆抗体的II期和III期随机临床试验,以更新我们之前涵盖2005年至2018年发表研究的荟萃分析。共识别出566篇文献,其中六项近期试验(除之前识别的30项外)涉及美泊利单抗、贝那利珠单抗、瑞利珠单抗和度普利尤单抗,符合我们的纳入标准。由于未从文献中检索到直接对比试验,我们进行了基于组的网状荟萃分析,共纳入19项随机对照试验,以比较不同治疗方法对急性加重率的影响。

证据综合

在我们的网状荟萃分析中,与汇总安慰剂相比,贝那利珠单抗显著降低了急性加重风险(中位效应差值:-0.520,95%置信区间[-1.010--0.048])。在间接比较中,没有一种生物制剂显示出优于其他制剂的效果。与安慰剂相比,观察到急性加重率大幅降低,不过只有贝那利珠单抗有足够的样本量(N = 2564),在总体人群以及与安慰剂相比的IL-5作用药物亚组分析中均显示急性加重率显著降低。

结论

在已发表的试验中,单克隆抗体已证明其在降低重度持续性嗜酸性粒细胞哮喘急性加重率方面的益处。没有一种生物制剂显示出优于其他制剂的效果,这强调了需要明确界定内型,以表明哪些患者将从每种治疗中获得最佳益处。

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