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.

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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
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article

Prospective REALITI-A Study

Guy Brusselle, Cristiano Caruso, Rupert W. Jakes, Thomas Köhler et al.
5 citations
CHEST Pulmonary
Asthma and respiratory diseases
1.63
article

Prospective REALITI-A Study

Guy Brusselle, Cristiano Caruso, Rupert W. Jakes, Thomas Köhler, Manish Patel, Giorgio Walter Canonica, Geoffrey Chupp, Rafael Alfonso‐Cristancho, Lydia Demetriou, Andrew Smith, Charles Pilette, Robert G. Price, Peter Howarth, Antonio Valero, Mark C. Liu
article en
5 citations

Abstract

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.

CHEST PulmonaryVol. 3(1)
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)
Zero hunger
Openalex Percentile: Top 16%
Asthma and respiratory diseases
1.63
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