Comparative efficacy of biologics for patients with inadequately controlled asthma: A network meta-analysis

IF 3.9 2区 医学 Q2 ALLERGY World Allergy Organization Journal Pub Date : 2024-07-01 DOI:10.1016/j.waojou.2024.100934
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Abstract

Background

Few studies have evaluated the comparative efficacy of biologics for asthma. This network meta-analysis aimed to compare the efficacy of biologics.

Methods

This study included randomized controlled trials (RCTs) evaluating the efficacy of a biologic compared to a placebo or another biologic in patients with inadequately controlled asthma despite high-intensity treatment, published by January 6, 2022. Two researchers independently searched the PubMed, Embase, Web of Science, and Scopus and assessed the risk of bias using the Cochrane tool. The outcomes of interest were the annual asthma exacerbation rate (AER), forced expiratory volume per second before bronchodilator use (preBD FEV1), the asthma control questionnaire (ACQ), and asthma quality of life questionnaire (AQLQ) results. A frequentist network meta-analysis was conducted, and a random effects model was used to draw pooled incidence rate ratio or standardized mean differences.

Results

Twenty-three RCTs with 8376 participants were retrieved. All biologics included in this study were associated with significantly better effects than placebo in AER, preBD FEV1, and ACQ outcomes. Although there were no significant differences between the biologics in the overall study population, patients with eosinophil levels ≥300 cells/μL or eosinophilic asthma showed that dupilumab and tezepelumab were significantly better than anti-IL-5 biologics in improving preBD FEV1. Additionally, in patients with eosinophil levels ≥300 cells/μL, benralizumab, unlike reslizumab, performed significantly better than placebo in improving ACQ and AQLQ outcomes.

Conclusion

The comparative effects of biologics can be considered with phenotypes and biomarkers to help clinicians select an appropriate treatment for inadequately controlled asthma.

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生物制剂对未得到充分控制的哮喘患者的疗效比较:网络荟萃分析
背景很少有研究对生物制剂治疗哮喘的疗效进行比较评估。本网络荟萃分析旨在比较生物制剂的疗效。方法本研究纳入了2022年1月6日之前发表的随机对照试验(RCT),这些试验评估了生物制剂与安慰剂或另一种生物制剂相比对高强度治疗后仍未得到充分控制的哮喘患者的疗效。两名研究人员独立检索了 PubMed、Embase、Web of Science 和 Scopus,并使用 Cochrane 工具评估了偏倚风险。研究结果包括年度哮喘加重率(AER)、使用支气管扩张剂前每秒用力呼气容积(FEV1)、哮喘控制问卷(ACQ)和哮喘生活质量问卷(AQLQ)结果。研究人员进行了频数网络荟萃分析,并使用随机效应模型得出集合发病率比或标准化平均差。本研究纳入的所有生物制剂在AER、BD前FEV1和ACQ结果方面的效果均明显优于安慰剂。虽然在整个研究人群中,生物制剂之间没有明显差异,但在嗜酸性粒细胞水平≥300 cells/μL 或嗜酸性粒细胞性哮喘患者中,dupilumab 和 tezepelumab 在改善 BD 前 FEV1 方面的效果明显优于抗 IL-5 生物制剂。此外,对于嗜酸性粒细胞水平≥300 cells/μL 的患者,与雷利珠单抗不同,苯拉利珠单抗在改善 ACQ 和 AQLQ 结果方面明显优于安慰剂。
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来源期刊
World Allergy Organization Journal
World Allergy Organization Journal Immunology and Microbiology-Immunology
CiteScore
9.10
自引率
5.90%
发文量
91
审稿时长
9 weeks
期刊介绍: The official pubication of the World Allergy Organization, the World Allergy Organization Journal (WAOjournal) publishes original mechanistic, translational, and clinical research on the topics of allergy, asthma, anaphylaxis, and clincial immunology, as well as reviews, guidelines, and position papers that contribute to the improvement of patient care. WAOjournal publishes research on the growth of allergy prevalence within the scope of single countries, country comparisons, and practical global issues and regulations, or threats to the allergy specialty. The Journal invites the submissions of all authors interested in publishing on current global problems in allergy, asthma, anaphylaxis, and immunology. Of particular interest are the immunological consequences of climate change and the subsequent systematic transformations in food habits and their consequences for the allergy/immunology discipline.
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