Predictors of Response to Biologics for Severe Asthma: A Systematic Review and Meta‐Analysis

医学 哮喘 重症监护医学 人口 生物制剂 内科学 梅德林 临床试验 系统回顾 随机对照试验 荟萃分析 循证医学 疾病严重程度 嗜酸性粒细胞 过敏 预测值 风险评估
作者
Anna Rattu,Piers Dixey,David Charles,Christopher E. Brightling,Kian Fan Chung,Apostolos Bossios,Arnaud Bourdin,Ratko Djukanović,Sven‐Erik Dahlén,Louise Fleming,Rekha Chaudhuri,Erik Melén,A. Deschildre,Charles Pilette,Gerard H. Koppelman,Andrew Exley,Freja Anckers,Sarah Miller,Hanna Nielsen,Clare Williams
出处
期刊:Allergy [Wiley]
卷期号:81 (1): 24-55 被引量:5
标识
DOI:10.1111/all.70031
摘要

Biologics are effective for severe asthma, but not all patients benefit equally. There is an urgent need to understand which biologic works best for which patient. We systematically searched for predictors of response to biologics (except omalizumab) for severe asthma in four bibliographic databases and two trial registries from 1990 to 2024. Two reviewers screened records, extracted data, and assessed risk of bias using a modified CASP checklist. Data were synthesized narratively, and certainty of evidence assessed using the modified GRADE framework. Comparable studies were meta-analyzed using a random-effects model. From 5853 records, 21 studies were identified investigating predictors of anti-IL5/5Rα, 4Rα, and anti-TSLP response. We found predominantly 'moderate' to 'high' quality evidence that raised blood eosinophil counts (≥ 300 cells/μL), FeNO levels (> 40 ppb), lack of or low OCS dose (< 10 mg/day), and better asthma control predict biologic response. Evidence for the predictive value of other characteristics was limited and mostly 'low' quality. Key reasons for downgrading the evidence were heterogeneous response definitions and imprecision. No data were identified for the pediatric population or biologics targeting the non-T2 pathway. Outside of traditional inflammatory and clinical variables, there is an unmet need for universally applicable predictors of biologic response for severe asthma.
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