Effectiveness and safety of dupilumab for the treatment of severe asthma in a real-life French multi-centre adult cohort

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Abstract

Background: Dupilumab is a monoclonal anti-IL-4Rα antibody developed for the treatment of severe asthma (SA). An early access programme for dupilumab was opened in France in SA patients experiencing unacceptable steroids side-effects and/or life-threatening exacerbations. Objective: To assess changes in asthma control between baseline and 12 months of treatment. Methods: Multi-centre (n = 13) retrospective real-life cohort study. This study is registered on ClinicalTrials.gov (NCT04022447). Results: Overall, 64 patients with SA (median age 51, interquartile range [44-61]; 53% females) received dupilumab as add-on therapy to maximal standard of care; and 76% were on oral daily steroids at baseline. After 12 months, median asthma control test score improved from 14 [7-16] to 22 [17-24] (P

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APA

Dupin, C., Belhadi, D., Guilleminault, L., Gamez, A. S., Berger, P., De Blay, F., … Taillé, C. (2020). Effectiveness and safety of dupilumab for the treatment of severe asthma in a real-life French multi-centre adult cohort. Clinical and Experimental Allergy, 50(7), 789–798. https://doi.org/10.1111/cea.13614

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