[Efficacy and clinical remission in patients with severe asthma and blood eosinophil counts ≥150 cells/μl treated with benralizumab: a sub-analysis of the Phase 3 MIRACLE study].
<b>Objective:</b> To evaluate the efficacy of benralizumab in patients with baseline bEOS ≥150 cells/μl using data from the MIRACLE study in Asia. <b>Methods:</b> MIRACLE was a phase Ⅲ clinical trial. From September 7, 2017 to January 30, 2023, patients aged 12-75 years with eosinophilic severe asthma receiving medium- to high-dosage inhaled corticosteroids and long-acting β<sub>2</sub> agonists were enrolled from 79 centres in Asia. They were randomized (1∶1) to receive either benralizumab 30 mg or placebo for 48 weeks. The endpoints included annual asthma exacerbation rate (AAER), pre-bronchodilator forced expiratory volume in 1 second (pre-BD FEV<sub>1</sub>), total asthma symptom score (TASS), St George's Respiratory Questionnaire (SGRQ) score, and the proportion of patients achieving clinical remission (defined as no asthma exacerbations, FEV<sub>1</sub> improvement ≥100 ml, and 6-item Asthma Control Questionnaire [ACQ-6 score;≤0.75 or <1.5]; at Weeks 24 and 48) in patients with no baseline oral corticosteroid (OCS) use. <b>Results:</b> Of 695 patients randomized, 598 patients had baseline bEOS ≥150 cells/μl [benralizumab <i>n</i>=301, placebo <i>n</i>=297; age: (50.9±12.1) years; 61.2% were women]. In this population, benralizumab reduced the AAER by 67% [rate ratio (<i>RR</i>)=0.33, 95%<i>CI</i>: 0.25-0.44, <i>P</i><0.001) and improved lung function [least squares (LS) mean difference <i>vs.</i> placebo: 0.21 L, 95%<i>CI</i>: 0.14-0.29, <i>P</i><0.001]. Benralizumab achieved greater reductions in TASS (LS mean difference:-0.29, 95%<i>CI</i>:-0.46--0.11, <i>P</i>=0.002) and ACQ-6 scores (LS mean difference:-0.33, 95%<i>CI</i>:-0.46--0.19, <i>P</i><0.001), and improved SGRQ scores (LS mean difference:-8.07, 95%<i>CI</i>:-11.35--4.79], <i>P</i><0.001). Among patients with no baseline OCS use (benralizumab <i>n</i>=277; placebo <i>n</i>=264), a higher proportion of benralizumab-treated patients achieved clinical remission at Weeks 24 and 48 compared to the placebo-treated patients. <b>Conclusion:</b> These results reinforce that benralizumab can improve clinical outcomes in patients with severe, uncontrolled asthma with bEOS ≥150 cells/μl in Asia.
Authors
- Xiao Xu (ORCID: https://orcid.org/0000-0002-2761-2811)
- Sofia Necander
- Andrew Menzies‐Gow (ORCID: https://orcid.org/0000-0001-9707-4986)
- Zhengrong Luo (ORCID: https://orcid.org/0000-0001-5083-7368)
- Ziwen Zhao (ORCID: https://orcid.org/0000-0002-4374-9914)
- L M Wang
- Viktoría Werkström
- Kefang Lai (ORCID: https://orcid.org/0000-0001-7994-7296)
- Xiuhua Fu (ORCID: https://orcid.org/0000-0002-3856-2741)
- C T Liu (ORCID: https://orcid.org/0000-0002-6866-0641)
- Ping Chen (ORCID: https://orcid.org/0000-0001-8036-0855)
- Nanshan Zhong (ORCID: https://orcid.org/0000-0003-2274-1427)
- David Cohen (ORCID: https://orcid.org/0000-0001-7318-8567)
- Yen-Ching Wu
Institutions
- Kunming Medical University (CN)
- Guangzhou First People's Hospital (CN)
- First Affiliated Hospital of Kunming Medical University (CN)
- Xuzhou Central Hospital (CN)
- South China University of Technology (CN)
- Guangzhou Medical University (CN)
Publication Details
- Journal
- PubMed
- Published
- 2025-10-12
- DOI
- https://doi.org/10.3760/cma.j.cn112147-20250416-00210
- Primary Topic
- Asthma and respiratory diseases
- Type
- article
- Field-Weighted Citation Impact
- 0.00