Evidence map›Paper›PMID 42153327›Full record

Trial reportAmerican journal of respiratory and critical care medicine2026

Dupilumab in chronic obstructive pulmonary disease: a pooled analysis of emergency department visits, hospital admissions, and systemic corticosteroid use.

Surya P Bhatt, Fernando J Martinez, Imran Satia, Antonio Anzueto, Jean Bourbeau, Alberto Papi, Stephanie Korn, Gaëtan Deslée, Changming Xia, Jigna Heble and 2 more

2 registry-linked trialsAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in American journal of respiratory and critical care medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03930732 phase3completednot on this map

A Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Pivotal Study to Assess the Efficacy, Safety and Tolerability of Dupilumab in Patients With Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD) With Type 2 Inflammation

TypeinterventionalSponsorSanofiRan2019 to 2023Enrolled939ConditionsChronic Obstructive Pulmonary DiseaseArmsDupilumab SAR231893, Inhaled Corticosteroid, Inhaled Long-Acting Beta Agonist, Inhaled Long-Acting Muscarinic Antagonist, Placebo
NCT04456673 phase3completednot on this map

A Randomized, Double-blind, Placebo-controlled, Parallel-group, 52-week Pivotal Study to Assess the Efficacy, Safety, and Tolerability of Dupilumab in Patients With Moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD) With Type 2 Inflammation

TypeinterventionalSponsorSanofiRan2020 to 2024Enrolled935ConditionsChronic Obstructive Pulmonary DiseaseArmsDupilumab SAR231893, Inhaled Corticosteroid, Inhaled Long-Acting Beta Agonist, Inhaled Long-Acting Muscarinic Antagonist, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Surya P BhattDivision of Pulmonary, Allergy and Critical Care Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.ORCID 0000-0002-8418-4497
Fernando J MartinezDivision of Allergy, Pulmonary and Critical Care Medicine, University of Massachusetts Chan/UMass Memorial Hospital, Worcester, MA, United States.
Imran SatiaDivision of Respirology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Antonio AnzuetoDivision of Pulmonary Diseases and Critical Care Medicine, University of Texas Health, San Antonio, TX, United States.
Jean BourbeauRespiratory Epidemiology and Clinical Research Unit, Department of Medicine, McGill University and Research Institute of the McGill University Health Centre, Montreal, QC, Canada.ORCID 0000-0002-7649-038X
Alberto PapiDepartment of Cardiorespiratory Medicine, Respiratory Medicine Unit, University of Ferrara, S. Anna University Hospital, Ferrara, Italy.
Stephanie KornIKF Pneumologie Mainz, Mainz, Germany.
Gaëtan DesléeDepartment of Pulmonary Medicine, INSERM U1250 U903, University Hospital of Reims, Reims, France.
Changming XiaRegeneron Pharmaceuticals Inc., Tarrytown, NY, United States.
Jigna HebleSanofi, Morristown, NJ, United States.
Mena SolimanRegeneron Pharmaceuticals Inc., Tarrytown, NY, United States.
Mona BafadhelKing's Centre for Lung Health, School of Immunology and Microbial Sciences, Faculty of Life Sciences & Medicine, King's College London, London, United Kingdom.

Funding

1/2 Video Telehealth Pulmonary Rehabilitation to Reduce Hospital Readmission in Chronic Obstructive Pulmonary Disease (Tele-COPD)UH3HL155806 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Surya P Bhatt · 2022 to 2026
$5.4M
Structural Determinants of Disease Progression in COPDR01HL151421 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BHATT, SURYA P., NAKHMANI, ARIE · 2020 to 2024
$2.6M
Asthma + Lung UKAstraZenecaBoehringer IngelheimGood Publication Practice GPP2022National Health ServiceNational Institute for HealthNHLBI NIH HHS R01 HL151421NHLBI NIH HHS UH3 HL155806NIH HHS R01HL151421NIH HHS UH3HL155806NIHRSanofi and Regeneron Pharmaceuticals IncUK Department of Health and Social Care
6 · The paper itself

Abstract

rationaleIn chronic obstructive pulmonary disease (COPD), exacerbations drive morbidity, healthcare resource utilization, and mortality. Hospitalization and emergency department (ED) visits reflect acute clinical instability. Systemic corticosteroids are usually prescribed for exacerbations, but cumulative exposure is a concern.

objectivesTo evaluate the effect of dupilumab on ED visits/hospital admissions and systemic corticosteroid use in patients experiencing exacerbations.

methodsBOREAS and NOTUS, two phase 3, randomized, double-blind, placebo-controlled trials, enrolled patients (40-85 years) with COPD, moderate-to-severe airflow limitation, and type 2 inflammation (screening blood eosinophil count ≥300 cells/µL). Patients received dupilumab 300 mg (N = 938) or placebo (N = 936) for 52 weeks. Systemic corticosteroid use and annualized rate and time to first ED visit/hospital admission were assessed. MEASUREMENTS AND MAIN

resultsDupilumab versus placebo reduced ED visits/hospital admissions of any duration by 38% (rate ratio, 0.62 [95% CI, 0.43-0.90]; P = .0121), delayed time to first event, and reduced risk of a first event by 45% (hazard ratio, 0.55 [95% CI, 0.38-0.78]; P = .0010). Compared with placebo, systemic corticosteroid use was reduced in patients treated with dupilumab who experienced severe exacerbations by 42% (rate ratio, 0.58 [95% CI, 0.38-0.89]; P = .0126) and moderate exacerbations by 28% (rate ratio, 0.72 [95% CI, 0.60-0.87]; P = .0005).

conclusionsDupilumab reduced ED visits/hospital admissions of any duration. Patients who experienced moderate and/or severe exacerbations required fewer systemic corticosteroids with dupilumab compared with placebo. CLINICAL

trial registrationClinicalTrials.gov (NCT03930732, NCT04456673).

Indexed as

Adrenal Cortex HormonesAntibodies, Monoclonal, HumanizedEmergency Room VisitsHospitalizationPulmonary Disease, Chronic ObstructiveAdultAgedAged, 80 and overDisease ProgressionDouble-Blind MethodEmergency Service, HospitalFemaleHumansMaleMiddle AgedTreatment OutcomeAdrenal Cortex HormonesAntibodies, Monoclonal, Humanizeddupilumabchronic obstructive pulmonary diseasedupilumabexacerbationssevere exacerbationssystemic corticosteroids

Identifiers

PMID42153327
PMCPMC13519320

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.