Two-Year Integrated Efficacy And Safety Analysis Of Benralizumab In Severe Asthma
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Author
FitzGerald, J MarkBleecker, Eugene R
Bourdin, Arnaud
Busse, William W
Ferguson, Gary T
Brooks, Laura
Barker, Peter
Martin, Ubaldo J
Affiliation
Univ Arizona, Coll Med, Div PharmacogenUniv Arizona, Coll Med, Div Genet Genom & Precis Med
Issue Date
2019-12-09
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DOVE MEDICAL PRESS LTDCitation
FitzGerald, J. M., Bleecker, E. R., Bourdin, A., Busse, W. W., Ferguson, G. T., Brooks, L., … Martin, U. J. (2019). Two-Year Integrated Efficacy And Safety Analysis Of Benralizumab In Severe Asthma. Journal of Asthma and Allergy, Volume 12, 401–413. https://doi.org/10.2147/jaa.s227170 Journal
JOURNAL OF ASTHMA AND ALLERGYRights
Copyright © 2019 FitzGerald et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/).Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Background: Benralizumab is an interleukin-5 receptor alpha-directed cytolytic monoclonal antibody. Treatment with benralizumab significantly reduces exacerbations and improves lung function after 1 year for patients with severe, uncontrolled eosinophilic asthma. Objective: We explored whether benralizumab efficacy was sustained after an additional year of treatment while maintaining an acceptable safety profile. Methods: Data from the pivotal 48-week SIROCCO and 56-week CALIMA studies were integrated with data from the predefined 56-week adult phase of the BORA extension study to provide a 2-year integrated efficacy and safety analysis of benralizumab. BORA enrolled patients who had completed SIROCCO or CALIMA. Patients receiving benralizumab 30 mg subcutaneously, either every 4 weeks (Q4W) or every 8 weeks (Q8W; first three doses Q4W), were assessed. Efficacy was evaluated based on baseline blood eosinophil counts from the pivotal studies (>= 300 and <300 cells/mu L). Results: Mean treatment exposures were 24.3 (Q4W, n=518) and 24.6 (Q8W, n=512) months. Exacerbation frequency reductions observed in SIROCCO/CALIMA were maintained; 50% of the patients had no exacerbations during the 2-year study period (crude exacerbation rate, Q8W: 0.56 exacerbations/year for patients with blood eosinophil counts >= 300 cells/mu L). Lung function improvements with benralizumab were maintained for 2 years, as represented by increases in mean prebronchodilator forced expiratory volume in 1 second from baseline of 0.343 L and 0.364 L with 1 and 2 years of benralizumab Q8W treatment, respectively, for patients with blood eosinophil counts >= 300 cells/mu L. Health-related quality of life improvements with benralizumab observed in the pivotal studies were also sustained. Adverse events and serious adverse event rates were similar between the BORA extension and SIROCCO/CALIMA periods, with no new or unexpected occurrence of adverse events. Conclusion: This benralizumab 2-year integrated analysis further supports long-term use of benralizumab for patients with severe, uncontrolled eosinophilic asthma.Note
Open access journalISSN
1178-6965PubMed ID
31849500Version
Final published versionSponsors
AstraZeneca; Kyowa Hakko Kirinae974a485f413a2113503eed53cd6c53
10.2147/JAA.S227170
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Except where otherwise noted, this item's license is described as Copyright © 2019 FitzGerald et al. This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/).
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