Multi-Criteria Decision Analysis of Biologics in Chronic Obstructive Pulmonary Disease.

IF 3.1 3区 医学 Q2 RESPIRATORY SYSTEM
Maria Gabriella Matera, Luigino Calzetta, Paola Rogliani, Mario Cazzola
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引用次数: 0

Abstract

Background: Chronic obstructive pulmonary disease (COPD) is a heterogeneous condition with limited response to standard anti-inflammatory therapies. Biologics targeting specific inflammatory pathways have emerged as potential treatments, but their efficacy remains variable across distinct COPD endotypes.

Objective: To systematically evaluate the efficacy and trial quality of biologics tested in COPD patients using a multicriteria decision analysis (MCDA) approach, with attention to type 2 (T2) and non-T2 inflammatory targets.

Methods: We assessed 20 trials encompassing 12 biologics and 9294 patients with COPD. Each trial was scored (0-3 per domain, total 12 points) across four domains: exacerbation reduction, lung function improvement, biomarker stratification, and trial design quality.

Results: Dupilumab (anti-IL-4Rα) demonstrated the most robust efficacy in eosinophilic COPD, with consistent reductions in exacerbation rates and improvements in FEV1, supported by high trial quality. Mepolizumab and benralizumab (anti-IL-5/IL-5R) showed moderate efficacy in biomarker-enriched populations. Anti-alarmins, specifically tozorakimab (anti-IL-33), itepekimab (anti-IL-33/IL-1RL1), astegolimab (anti-ST2), and tezepelumab (anti-TSLP), showed mixed results, with modest lung function gains but largely non-significant effects on exacerbation rates. Agents targeting non-T2 pathways, including infliximab (anti-TNF-α), canakinumab (anti-IL-1β), MEDI8968 (anti-IL-1R1), CNTO6785 (anti-IL-17A), and ABX-IL8 (anti-IL-8), consistently failed to demonstrate clinical efficacy, often due to small sample sizes, early-phase design, and lack of biomarker stratification.

Conclusion: Biologics targeting T2 inflammation offer therapeutic promise in eosinophilic COPD when guided by biomarkers. Conversely, current biologics directed at non-T2 and alarmin pathways yield limited or inconsistent benefits, emphasizing the need for improved phenotyping and targeted intervention strategies in non-eosinophilic COPD.

Abstract Image

慢性阻塞性肺疾病生物制剂的多标准决策分析。
背景:慢性阻塞性肺疾病(COPD)是一种异质性疾病,对标准抗炎治疗的反应有限。针对特定炎症途径的生物制剂已成为潜在的治疗方法,但其疗效在不同的COPD内型中仍存在差异。目的:采用多标准决策分析(MCDA)方法,关注2型(T2)和非T2炎症靶点,系统评价生物制剂在COPD患者中的疗效和试验质量。方法:我们评估了20项试验,包括12种生物制剂和9294例COPD患者。每个试验在四个领域进行评分(每个领域0-3分,共12分):减少恶化,肺功能改善,生物标志物分层和试验设计质量。结果:Dupilumab(抗il - 4r α)在嗜酸性COPD中表现出最强大的疗效,在高质量的试验支持下,其恶化率持续降低,FEV1改善。Mepolizumab和benralizumab(抗il -5/IL-5R)在生物标志物富集人群中显示中等疗效。抗危险药物,特别是托zorakimab(抗il -33), itepekimab(抗il -33/IL-1RL1),阿斯特戈利单抗(抗st2)和tezepelumab(抗tslp),显示出混合的结果,肺功能得到适度的改善,但对恶化率的影响很大程度上不显著。靶向非t2通路的药物,包括英菲利昔单抗(抗tnf -α)、canakinumab(抗il -1β)、MEDI8968(抗il - 1r1)、CNTO6785(抗il - 17a)和ABX-IL8(抗il -8),一直未能证明临床疗效,通常是由于样本量小、早期设计和缺乏生物标志物分层。结论:在生物标志物的指导下,靶向T2炎症的生物制剂有望治疗嗜酸性COPD。相反,目前针对非t2和警报蛋白通路的生物制剂产生有限或不一致的益处,强调需要改善非嗜酸性COPD的表型和有针对性的干预策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
10.70%
发文量
372
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal of therapeutics and pharmacology focusing on concise rapid reporting of clinical studies and reviews in COPD. Special focus will be given to the pathophysiological processes underlying the disease, intervention programs, patient focused education, and self management protocols. This journal is directed at specialists and healthcare professionals
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