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. 2024 Apr;132(4):463-468.e1.
doi: 10.1016/j.anai.2023.11.006. Epub 2023 Nov 14.

Real-world effectiveness of dupilumab in patients with asthma: Findings from the US ADVANTAGE study

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Real-world effectiveness of dupilumab in patients with asthma: Findings from the US ADVANTAGE study

Michael Blaiss et al. Ann Allergy Asthma Immunol. 2024 Apr.

Abstract

Background: Dupilumab is approved as an add-on maintenance therapy for patients (≥6 years) with moderate-to-severe asthma. Better understanding of real-world effectiveness is needed.

Objective: To characterize the real-world effectiveness of dupilumab in asthma management.

Methods: This retrospective study included patients (≥12 years of age) diagnosed with asthma, initiating dupilumab between November 2018 and September 2020. The study used a US electronic medical record database (TriNetX Dataworks, Cambridge, Massachusetts). Asthma exacerbation rates before and after the initiation of dupilumab were analyzed using generalized estimating equations models with Poisson probabilistic link to estimate incidence rate ratios (IRRs). Sensitivity analyses were conducted based on previous exacerbation data, eosinophil levels, history of atopic dermatitis or chronic rhinosinusitis with nasal polyps, previous use of biologics, and presence of SARS-CoV-2 (COVID-19).

Results: A total of 2400 patients initiating dupilumab met all study criteria. After initiation of dupilumab, risk of asthma exacerbation was reduced by 44% (IRR, 0.56; 95% CI, 0.47-0.57; P = <0.0001) and systemic corticosteroid prescriptions by 48% (IRR, 0.52; 95% CI, 0.48, 0.56; P = <0.0001) compared with those before initiation of dupilumab. Adjustment for COVID-19 showed a greater reduction in asthma exacerbations (IRR, 0.50; 95% CI, 0.45-0.55; P = <0.0001).

Conclusion: Current real-world efficacy evidence indicates that dupilumab reduces asthma exacerbations and total systemic corticosteroid prescriptions in clinical practice. The effectiveness of dupilumab was observed independent of exacerbation history, eosinophil levels, or COVID-19 impact.

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Conflict of interest statement

Disclosures Dr Blaiss: Sanofi, Regeneron, Amgen, Lanier Biotherapeutics; Eugene R. Bleecker: Sanofi, AstraZeneca, Novartis, Regeneron; Dr Jacob-Nara and Dr Hardin are employees of Sanofi; Dr Borsos and Dr Nair were employees of Sanofi at the time of study and preparation of the manuscript; Dr Wang and Dr Soler are employees and stockholders of Regeneron; Mei Sheng Duh, Mingchen Ye, and Anamika Khanal are employees of Analysis Group, Inc, which received research funds from Sanofi to conduct this study; Dr Stanford is a paid consultant for Sanofi.

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