Dupilumab improves long-term outcomes in patients with uncontrolled, moderate-to-severe GINA-based type 2 asthma, irrespective of allergic status.


Journal

Allergy
ISSN: 1398-9995
Titre abrégé: Allergy
Pays: Denmark
ID NLM: 7804028

Informations de publication

Date de publication:
08 2023
Historique:
revised: 06 04 2023
received: 28 09 2022
accepted: 07 04 2023
medline: 1 8 2023
pubmed: 19 4 2023
entrez: 19 04 2023
Statut: ppublish

Résumé

Previous research has shown greater efficacy of dupilumab in patients with uncontrolled asthma and type 2 inflammation. We analyzed dupilumab's efficacy in patients from the TRAVERSE study with or without evidence of allergic asthma and type 2 inflammation per current GINA guidelines (≥150  eosinophils/μL or FeNO ≥20 ppb). All patients aged ≥12 years who rolled over from the placebo-controlled QUEST study (NCT02414854) to TRAVERSE (NCT02134028) received add-on dupilumab 300 mg every 2 weeks for up to 96 weeks. We assessed annualized severe asthma exacerbation rates (AERs) and changes from parent-study baseline (PSBL) in pre-bronchodilator FEV In TRAVERSE, dupilumab consistently reduced AER across all subgroups. By Week 96, dupilumab increased pre-bronchodilator FEV Long-term treatment with dupilumab reduced exacerbation rates and improved lung function and asthma control in patients with asthma with type 2 inflammation as per current GINA guidance and irrespective of evidence of allergic asthma.

Sections du résumé

BACKGROUND
Previous research has shown greater efficacy of dupilumab in patients with uncontrolled asthma and type 2 inflammation. We analyzed dupilumab's efficacy in patients from the TRAVERSE study with or without evidence of allergic asthma and type 2 inflammation per current GINA guidelines (≥150  eosinophils/μL or FeNO ≥20 ppb).
METHODS
All patients aged ≥12 years who rolled over from the placebo-controlled QUEST study (NCT02414854) to TRAVERSE (NCT02134028) received add-on dupilumab 300 mg every 2 weeks for up to 96 weeks. We assessed annualized severe asthma exacerbation rates (AERs) and changes from parent-study baseline (PSBL) in pre-bronchodilator FEV
RESULTS
In TRAVERSE, dupilumab consistently reduced AER across all subgroups. By Week 96, dupilumab increased pre-bronchodilator FEV
CONCLUSIONS
Long-term treatment with dupilumab reduced exacerbation rates and improved lung function and asthma control in patients with asthma with type 2 inflammation as per current GINA guidance and irrespective of evidence of allergic asthma.

Identifiants

pubmed: 37073882
doi: 10.1111/all.15747
doi:

Substances chimiques

dupilumab 420K487FSG
Bronchodilator Agents 0
Antibodies, Monoclonal 0
Anti-Asthmatic Agents 0

Banques de données

ClinicalTrials.gov
['NCT02414854', 'NCT02134028']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2148-2156

Informations de copyright

© 2023 Sanofi and The Authors. Allergy published by European Academy of Allergy and Clinical Immunology and John Wiley & Sons Ltd.

Références

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Auteurs

Klaus F Rabe (KF)

LungenClinic Grosshansdorf (Member of the German Center for Lung Research [DZL]), Airway Research Center North (ARCN), Grosshansdorf, Germany.
Christian-Albrechts University (Member of the German Center for Lung Research [DZL]), Airway Research Center North (ARCN), Kiel, Germany.

Ian D Pavord (ID)

NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.

William W Busse (WW)

University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.

Geoffrey L Chupp (GL)

Yale School of Medicine, New Haven, Connecticut, USA.

Kenji Izuhara (K)

Saga Medical School, Saga, Japan.

Arman Altincatal (A)

Sanofi, Cambridge, Massachusetts, USA.

Rebecca Gall (R)

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

Nami Pandit-Abid (N)

Sanofi, Bridgewater, New Jersey, USA.

Yamo Deniz (Y)

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.

Amr Radwan (A)

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

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