From FEV1 to Small Airways: AMethodological Review of Lung Function Assessment in Biologic-Treated Asthma.

IF 3.3 3区 医学 Q2 ALLERGY
Journal of Asthma and Allergy Pub Date : 2026-08-14 eCollection Date: 2026-01-01 DOI:10.2147/JAA.S628156
Hai-Ling Yang, Ya-Jia Chen, Xue-Qiong Mai, Xiao-Ling Zou, Wenwen Ding, Shao-Zhu Wu
{"title":"From FEV<sub>1</sub> to Small Airways: AMethodological Review of Lung Function Assessment in Biologic-Treated Asthma.","authors":"Hai-Ling Yang, Ya-Jia Chen, Xue-Qiong Mai, Xiao-Ling Zou, Wenwen Ding, Shao-Zhu Wu","doi":"10.2147/JAA.S628156","DOIUrl":null,"url":null,"abstract":"<p><p>Biologics have revolutionized the treatment of severe asthma, yet their clinical efficacy assessment has focused primarily on exacerbation reduction and symptom control, often overlooking the comprehensive evaluation of lung function improvement. Traditionally, forced expiratory volume in onesecond (FEV<sub>1</sub>) has been the cornerstone metric for assessing airflow limitation. However, accumulating evidence highlights small airway dysfunction (SAD) as acritical driver of asthma symptoms, exacerbation risk, and heterogeneity in treatment response. This review explores the existing tools and metrics and their clinical relevance for assessing the impact of biologics on lung function, with aparticular emphasis on small airway function in asthma patients. Methodologically, we appraise the physiological validity, repeatability, feasibility, responsiveness, and current regulatory readiness of small-airway endpoints for biologic trials and real-world effectiveness studies. We propose that these measures complement, rather than replace, FEV<sub>1</sub> within amultidimensional endpoint framework. We explore the application of techniques ranging from conventional spirometry (FEV<sub>1</sub>, FEF<sub>2</sub> <sub>5</sub>-<sub>7</sub> <sub>5</sub>, ie, forced expiratory flow at 25-75% of forced vital capacity) to more advanced methods such as impulse oscillometry (IOS), body plethysmography, multiple-breath nitrogen washout (MBNW), and novel imaging modalities. Our analysis reveals the differences in the effects of various biologics (anti-IgE, anti-IL-5/5Rα, anti-IL-4Rα, anti-TSLP, etc.). on large and small airways. Furthermore, we also discuss the methodological frameworks, challenges, and future directions for integrating small airway function assessment into both clinical trial design and real-world effectiveness evaluations.</p>","PeriodicalId":15079,"journal":{"name":"Journal of Asthma and Allergy","volume":"19 ","pages":"628156"},"PeriodicalIF":3.3000,"publicationDate":"2026-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13487953/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Asthma and Allergy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2147/JAA.S628156","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"ALLERGY","Score":null,"Total":0}
引用次数: 0

Abstract

Biologics have revolutionized the treatment of severe asthma, yet their clinical efficacy assessment has focused primarily on exacerbation reduction and symptom control, often overlooking the comprehensive evaluation of lung function improvement. Traditionally, forced expiratory volume in onesecond (FEV1) has been the cornerstone metric for assessing airflow limitation. However, accumulating evidence highlights small airway dysfunction (SAD) as acritical driver of asthma symptoms, exacerbation risk, and heterogeneity in treatment response. This review explores the existing tools and metrics and their clinical relevance for assessing the impact of biologics on lung function, with aparticular emphasis on small airway function in asthma patients. Methodologically, we appraise the physiological validity, repeatability, feasibility, responsiveness, and current regulatory readiness of small-airway endpoints for biologic trials and real-world effectiveness studies. We propose that these measures complement, rather than replace, FEV1 within amultidimensional endpoint framework. We explore the application of techniques ranging from conventional spirometry (FEV1, FEF2 5-7 5, ie, forced expiratory flow at 25-75% of forced vital capacity) to more advanced methods such as impulse oscillometry (IOS), body plethysmography, multiple-breath nitrogen washout (MBNW), and novel imaging modalities. Our analysis reveals the differences in the effects of various biologics (anti-IgE, anti-IL-5/5Rα, anti-IL-4Rα, anti-TSLP, etc.). on large and small airways. Furthermore, we also discuss the methodological frameworks, challenges, and future directions for integrating small airway function assessment into both clinical trial design and real-world effectiveness evaluations.

从FEV1到小气道:生物治疗哮喘肺功能评估的方法学综述。
生物制剂已经彻底改变了重症哮喘的治疗,但其临床疗效评估主要集中在减轻加重和控制症状上,往往忽视了对肺功能改善的综合评估。传统上,一秒用力呼气量(FEV1)一直是评估气流限制的基础指标。然而,越来越多的证据表明,小气道功能障碍(SAD)是哮喘症状、恶化风险和治疗反应异质性的关键驱动因素。本综述探讨了评估生物制剂对肺功能影响的现有工具和指标及其临床相关性,特别强调哮喘患者的小气道功能。在方法学上,我们评估了生理有效性、可重复性、可行性、反应性和小气道终点在生物试验和现实世界有效性研究中的当前监管就绪性。我们建议这些措施在多维端点框架内补充而不是取代FEV1。我们探索了从传统肺活量测定法(FEV1, FEF2 5-75,即用力呼气流量在用力肺活量的25-75%)到更先进的方法,如脉冲振荡测定法(IOS),身体体积脉搏图,多次呼吸氮冲洗(MBNW)和新型成像方式等技术的应用。我们的分析揭示了不同生物制剂(抗ige、抗il -5/ 5r α、抗il - 4r α、抗tslp等)的作用差异。在大气道和小气道上。此外,我们还讨论了将小气道功能评估纳入临床试验设计和现实世界有效性评估的方法学框架、挑战和未来方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Asthma and Allergy
Journal of Asthma and Allergy Medicine-Immunology and Allergy
CiteScore
5.30
自引率
6.20%
发文量
185
审稿时长
16 weeks
期刊介绍: An international, peer-reviewed journal publishing original research, reports, editorials and commentaries on the following topics: Asthma; Pulmonary physiology; Asthma related clinical health; Clinical immunology and the immunological basis of disease; Pharmacological interventions and new therapies. Although the main focus of the journal will be to publish research and clinical results in humans, preclinical, animal and in vitro studies will be published where they shed light on disease processes and potential new therapies.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书