Overcoming Barriers to Remission in Severe Eosinophilic Asthma: Two‐Year Real‐World Data With Benralizumab

Author:

Jackson David J.12,Burhan Hassan34,Rupani Hitasha5ORCID,Pfeffer Paul E.6,Clifton Ian J.7ORCID,Faruqi Shoaib8,Dhariwal Jaideep1,Patel Pujan9,Morris Tamsin10,Lipworth Joseph10,Watt Michael10,Lupton Charlotte10,Dube Sabada10,Hickey Joe11,Nanzer Alexandra M.12

Affiliation:

1. Guy's Severe Asthma Centre Guy's & St Thomas' NHS Trust London UK

2. School of Immunology & Microbial Sciences King's College London London UK

3. Liverpool University Hospitals NHS Foundation Trust Liverpool UK

4. University of Liverpool Liverpool UK

5. University Hospital Southampton NHS Foundation Trust Southampton UK

6. St. Bartholomew's Hospital London UK

7. University of Leeds Leeds UK

8. Hull University Teaching Hospitals Hull UK

9. Royal Brompton and Harefield Hospitals London UK

10. AstraZeneca UK London UK

11. OPEN Health Marlow UK

Abstract

ABSTRACTBackgroundBenralizumab has been reported to lead to clinical remission of severe eosinophilic asthma (SEA) at 1 year in some patients. However, whether this is maintained over a longer term remains unclear. Additionally, the impact of pulmonary and extrapulmonary comorbidities on the ability to meet remission is poorly understood.MethodsClinical outcomes including remission of SEA with benralizumab at 1 and 2 years were assessed retrospectively in a real‐world UK multi‐centre severe asthma cohort. The presence of clinically relevant pulmonary and extrapulmonary comorbidities associated with respiratory symptoms was recorded. Analyses to identify factors associated with the ability to meet remission were performed.ResultsIn total, 276 patients with SEA treated with benralizumab including 113 patients who had switched from a previous biologic to benralizumab were included. Overall, clinical remission was met in 17% (n = 31/186) and 32% (n = 43/133) of patients at 1 and 2 years, respectively. This increased to 28% at 1 year and 49% at 2 years once patients with pulmonary and/or extrapulmonary comorbidities were excluded. Body mass index (BMI) and maintenance OCS (mOCS) use demonstrated a negative association with clinical remission at 1 (BMI: OR: 0.89, 95% CI: 0.82–0.96, p < 0.01; mOCS: OR: 0.94, 95% CI: 0.89–0.99, p < 0.05) and 2 years (BMI: OR: 0.93, 95% CI: 0.87–0.99, p < 0.05; mOCS: OR: 0.95, 95% CI: 0.89–0.99, p < 0.05).ConclusionsIn this long‐term, real‐world study, patients with SEA demonstrated the ability to meet and sustain clinical remission when treated with benralizumab. The presence of comorbidities including obesity, which are known to be independently associated with respiratory symptoms, reduced the likelihood of meeting clinical remission.

Publisher

Wiley

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