Hai-Ling Yang, Ya-Jia Chen, Xue-Qiong Mai, Xiao-Ling Zou, Wenwen Ding, Shao-Zhu Wu
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.