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Meta-analysis of asthma-related hospitalization in mepolizumab studies of severe eosinophilic asthma.

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posted on 2016-11-16, 10:21 authored by S. W. Yancey, H. G. Ortega, O. N. Keene, B. Mayer, N. B. Gunsoy, Christopher E. Brightling, E. R. Bleecker, Pranabashis Haldar, I. D. Pavord
BACKGROUND: Studies show that mepolizumab can reduce the frequency of clinically significant exacerbations in patients with severe eosinophilic asthma, compared with placebo. However, important events such as hospitalizations and emergency room visits are rare and difficult to characterize in single studies. OBJECTIVE: We sought to compare hospitalization or hospitalization and/or emergency room visit rates in patients with severe eosinophilic asthma treated with mepolizumab or placebo in addition to standard of care for at least 24 weeks. METHODS: This study was conducted and reported in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses statement. PubMed and the GSK Clinical Study Register were searched for suitable studies. The primary end points were the rate of exacerbations requiring hospitalization and the rate of exacerbations requiring hospitalization/emergency room visit. The proportion of patients with 1 or more event was also assessed. All mepolizumab doses were combined and individual patient-level data were analyzed. RESULTS: Four studies (n = 1388) were eligible for inclusion. Mepolizumab significantly reduced the rate of exacerbations requiring hospitalization (relative rate, 0.49; 95% CI, 0.30-0.80; P = .004) and hospitalization/emergency room visit (relative rate, 0.49; 95% CI, 0.33-0.73; P < .001) versus placebo. Significant reductions of 45% and 38% were also observed for the proportion of patients experiencing 1 or more hospitalization and hospitalization and/or emergency room visit, respectively. CONCLUSIONS: Mepolizumab approximately halved exacerbations requiring hospitalization and/or emergency room visits compared with placebo in patients with severe eosinophilic asthma. This treatment addresses a key outcome in a patient population with a high unmet need (GSK Study 204664).

Funding

Editorial support (in the form of writing assistance, including the development of the initial draft on the basis of author feedback on an initial outline developed by the first author, collating and incorporating author comments on all drafts, grammatical editing, and referencing) was provided by Elizabeth Hutchinson, PhD, of Fishawack Indicia Ltd, funded by GSK.

History

Citation

Journal of Allergy and Clinical Immunology, 2016

Author affiliation

/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY/School of Medicine/Department of Infection, Immunity and Inflammation

Version

  • VoR (Version of Record)

Published in

Journal of Allergy and Clinical Immunology

Publisher

Elsevier for American Academy of Allergy, Asthma and Immunology, Mosby

issn

0091-6749

eissn

1097-6825

Acceptance date

2016-08-09

Copyright date

2016

Available date

2016-11-16

Publisher version

http://www.sciencedirect.com/science/article/pii/S0091674916308910

Language

en

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