Prospective REALITI-A Study
Mepolizumab, a monoclonal antibody targeting IL-5, is of proven clinical benefit in severe asthma; however, prospective, long-term, real-world data in severe asthma are required. What is the real-world benefit of 2 years of mepolizumab treatment in severe asthma? REALITI-A was a 2-year, international, prospective study enrolling adults with asthma on newly initiated mepolizumab 100 mg subcutaneously (physician decision). Outcomes in the 1-year premepolizumab vs 2-year follow-up periods included rates of clinically significant asthma exacerbations (CSEs) (deterioration requiring systemic corticosteroids and/or emergency department [ED] visit/hospitalization), exacerbations requiring ED visit/hospitalization, exacerbations requiring hospitalization, proportion of patients with no exacerbations, median daily maintenance oral corticosteroids (mOCSs) dose, proportion of patients discontinuing mOCSs completely, Asthma Control Questionnaire-5 score, FEV 1 , and adverse events (AEs). After 2 years’ follow-up, 73% of patients (599 of 822) had no record of mepolizumab discontinuation. During the 2-year follow-up vs premepolizumab period (N = 822), rates of CSEs, exacerbations requiring ED visit/hospitalization, or hospitalization only were reduced by 74%, 79%, and 73%, respectively (odds ratio for no CSEs, 10.0; 95% CI, 7.55- 13.25). Median daily mOCS dose decreased from 10.0 (quartile 1, 5.0; quartile 3, 14.7) mg at week 0 (n = 297) to 0.0 (quartile 1, 0.0; quartile 3, 5.0) mg at weeks 101 to 104 (n = 168), and the proportion of patients discontinuing mOCS increased progressively to 43% at 1 year and 57% at 2 years. There was a 1.53-point reduction in Asthma Control Questionnaire-5 scores from baseline at 2 years. At months 21 to 24, least square mean FEV 1 improved by 142 mL from baseline. Ninety (11%) and 7 (< 1%) patients experienced mepolizumab-related AEs and serious AEs during the follow-up period, respectively. In patients with severe asthma, real-world mepolizumab treatment for 2 years was well tolerated and was associated with sustained reductions in exacerbations and progressive reductions in mOCS use.
Authors
- Guy Brusselle (ORCID: https://orcid.org/0000-0001-7021-8505)
- Cristiano Caruso (ORCID: https://orcid.org/0000-0001-7631-029X)
- Rupert W. Jakes (ORCID: https://orcid.org/0000-0002-3837-8063)
- Thomas Köhler (ORCID: https://orcid.org/0000-0001-9012-4100)
- Manish Patel (ORCID: https://orcid.org/0000-0003-3012-7507)
- Giorgio Walter Canonica (ORCID: https://orcid.org/0000-0001-8467-2557)
- Geoffrey Chupp (ORCID: https://orcid.org/0000-0001-9968-6564)
- Rafael Alfonso‐Cristancho (ORCID: https://orcid.org/0000-0002-7060-5131)
- Lydia Demetriou (ORCID: https://orcid.org/0009-0004-4665-279X)
- Andrew Smith (ORCID: https://orcid.org/0000-0003-4648-4090)
- Charles Pilette (ORCID: https://orcid.org/0000-0001-6685-0356)
- Robert G. Price (ORCID: https://orcid.org/0000-0001-6418-6818)
- Peter Howarth (ORCID: https://orcid.org/0000-0003-0619-7927)
- Antonio Valero (ORCID: https://orcid.org/0000-0002-5543-0345)
- Mark C. Liu
Institutions
- Università Cattolica del Sacro Cuore (IT)
- Cliniques Universitaires Saint-Luc (BE)
- Humanitas University (IT)
- Age UK (GB)
- Ghent University Hospital (BE)
- University Medical Center Freiburg (DE)
- Wishaw General Hospital (GB)
- Agostino Gemelli University Polyclinic (IT)
- North Hertfordshire College (GB)
- Yale University (US)
- GlaxoSmithKline (United States) (US)
- Hospital Clínic de Barcelona (ES)
- GlaxoSmithKline (Germany) (DE)
- IRCCS Humanitas Research Hospital (IT)
Publication Details
- Journal
- CHEST Pulmonary
- Published
- 2024-09-16
- DOI
- https://doi.org/10.1016/j.chpulm.2024.100107
- Citations
- 5
- Primary Topic
- Asthma and respiratory diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.63