Impact of dupilumab across seasons in patients with type 2 uncontrolled, moderate-to-severe asthma.

Allergic asthma exacerbations

Journal

Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology
ISSN: 1534-4436
Titre abrégé: Ann Allergy Asthma Immunol
Pays: United States
ID NLM: 9503580

Informations de publication

Date de publication:
25 Nov 2023
Historique:
received: 29 03 2023
revised: 15 11 2023
accepted: 15 11 2023
medline: 28 11 2023
pubmed: 28 11 2023
entrez: 28 11 2023
Statut: aheadofprint

Résumé

Seasonal variability could influence asthma exacerbations. Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for IL-4/IL-13, key and central drivers of type 2 inflammation. In the 52-week QUEST study (NCT02414854), add-on dupilumab every 2 weeks vs placebo significantly reduced exacerbations and improved pre-bronchodilator FEV1 in patients with uncontrolled, moderate-to-severe asthma. TRAVERSE (NCT02134028), the open-label QUEST extension study, enrolled patients with moderate-to-severe asthma to investigate long-term safety and efficacy of dupilumab, including patients previously receiving placebo that initiated dupilumab therapy. This post-hoc analysis investigated long-term dupilumab efficacy in reducing exacerbations across yearly seasons in patients with type 2 inflammatory asthma with and without clinical evidence of allergic asthma. Unadjusted annualized rate and proportions of patients experiencing severe asthma exacerbations are reported by month, season, and for both hemispheres. The proportion of type 2 patients experiencing ≥1 severe asthma exacerbation during QUEST was 20.8% vs 10.0% in spring, 18.2% vs 7.3% in summer, 22.2% vs 12.6% in autumn, and 26.4% vs 12.0% in winter, for placebo- vs dupilumab-treated patients, respectively; P<0.001 for placebo vs dupilumab in all seasons. Reductions in the proportion of patients experiencing severe exacerbations across seasons in subgroups with and without evidence of allergic asthma were similar to the overall type 2 population. Reductions in severe exacerbations observed during QUEST were sustained during TRAVERSE, up to 96 weeks across both hemispheres. Dupilumab reduced asthma exacerbations, with no difference in the reduction between seasons, in patients with type 2 inflammation, with and without evidence of allergic asthma.

Sections du résumé

BACKGROUND BACKGROUND
Seasonal variability could influence asthma exacerbations. Dupilumab, a fully human monoclonal antibody, blocks the shared receptor component for IL-4/IL-13, key and central drivers of type 2 inflammation. In the 52-week QUEST study (NCT02414854), add-on dupilumab every 2 weeks vs placebo significantly reduced exacerbations and improved pre-bronchodilator FEV1 in patients with uncontrolled, moderate-to-severe asthma. TRAVERSE (NCT02134028), the open-label QUEST extension study, enrolled patients with moderate-to-severe asthma to investigate long-term safety and efficacy of dupilumab, including patients previously receiving placebo that initiated dupilumab therapy.
OBJECTIVE OBJECTIVE
This post-hoc analysis investigated long-term dupilumab efficacy in reducing exacerbations across yearly seasons in patients with type 2 inflammatory asthma with and without clinical evidence of allergic asthma.
METHODS METHODS
Unadjusted annualized rate and proportions of patients experiencing severe asthma exacerbations are reported by month, season, and for both hemispheres.
RESULTS RESULTS
The proportion of type 2 patients experiencing ≥1 severe asthma exacerbation during QUEST was 20.8% vs 10.0% in spring, 18.2% vs 7.3% in summer, 22.2% vs 12.6% in autumn, and 26.4% vs 12.0% in winter, for placebo- vs dupilumab-treated patients, respectively; P<0.001 for placebo vs dupilumab in all seasons. Reductions in the proportion of patients experiencing severe exacerbations across seasons in subgroups with and without evidence of allergic asthma were similar to the overall type 2 population. Reductions in severe exacerbations observed during QUEST were sustained during TRAVERSE, up to 96 weeks across both hemispheres.
CONCLUSION CONCLUSIONS
Dupilumab reduced asthma exacerbations, with no difference in the reduction between seasons, in patients with type 2 inflammation, with and without evidence of allergic asthma.

Identifiants

pubmed: 38013139
pii: S1081-1206(23)01470-9
doi: 10.1016/j.anai.2023.11.021
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023. Published by Elsevier Inc.

Auteurs

Anju T Peters (AT)

Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA. Electronic address: anjupeters@northwestern.edu.

Hironori Sagara (H)

Division of Respiratory Medicine and Allergology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Jonathan Corren (J)

David Geffen School of Medicine at UCLA, Los Angeles, California, USA.

Christian Domingo (C)

Pulmonary Service, Corporació Sanitària Parc Taulí, Sabadell, Universitat Autònoma de Barcelona (UAB), Barcelona, Spain.

Arman Altincatal (A)

Sanofi, Cambridge, Massachusetts, USA.

Xavier Soler (X)

Regeneron Pharmaceuticals Inc., Tarrytown, New York, USA.

Nami Pandit-Abid (N)

Sanofi, Bridgewater, New Jersey, USA.

Nora Crikelair (N)

Regeneron Pharmaceuticals Inc., Tarrytown, New York, USA.

Paul J Rowe (PJ)

Sanofi, Bridgewater, New Jersey, USA.

Juby A Jacob-Nara (JA)

Sanofi, Bridgewater, New Jersey, USA.

Yamo Deniz (Y)

Regeneron Pharmaceuticals Inc., Tarrytown, New York, USA.

Classifications MeSH