Evidence map›Paper›PMID 40761646›Full record

ArticleERJ open research2025

Real-world comparative effectiveness of biologic therapies in severe asthma: EU-ADVANTAGE.

Giorgio Walter Canonica, Johann Christian Virchow, Arnaud Bourdin, Juby Jacob-Nara, Kinga Borsos, Richard H Stanford, Zhixiao Wang, Mena Soliman, Lynn Huynh, Fariha Haque and 2 more

Abstract read
In one paragraph

Article in ERJ open research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Giorgio Walter CanonicaPersonalized Medicine, Asthma and Allergy, Humanitas University and Research Hospital IRCCS, Milan, Italy.ORCID https://orcid.org/0000-0001-8467-2557
Johann Christian VirchowDepartments of Pneumology/Intensive Care Medicine, Universitätsmedizin Rostock, Rostock, Germany.
Arnaud BourdinDepartment of Respiratory Diseases, CHU Montpellier, University of Montpellier, PhyMedExp, INSERM, CNRS, Montpellier, France.ORCID https://orcid.org/0000-0002-4645-5209
Juby Jacob-NaraSanofi, Bridgewater, NJ, USA.
Kinga BorsosSanofi, Cambridge, MA, USA.
Richard H StanfordAESARA Inc., Chapel Hill, NC, USA.
Zhixiao WangRegeneron Pharmaceuticals, Inc., Sleepy Hollow, NY, USA.
Mena SolimanRegeneron Pharmaceuticals, Inc., Sleepy Hollow, NY, USA.
Lynn HuynhAnalysis Group, Inc., Boston, MA, USA.
Fariha HaqueAnalysis Group, Inc., Boston, MA, USA.
Mei Sheng DuhAnalysis Group, Inc., Boston, MA, USA.
Wei-Han ChengSanofi, Cambridge, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In Europe, although multiple biologics have been approved for the treatment of severe asthma (SA), comparative data from real-world settings remain limited. This study compared the real-world effectiveness of dupilumab with that of omalizumab, benralizumab and mepolizumab in European patients with SA. Methods: In the EU-ADVANTAGE study, physicians from France, Italy, Germany, Spain and the Netherlands were recruited to review medical charts of patients (aged ≥12 years) who had physician-confirmed SA and initiated dupilumab, omalizumab, benralizumab or mepolizumab (index) between May 2019 and February 2022. Patients with ≥12 months of pre- and post-index records were included. Differences in baseline covariates were balanced with inverse probability of treatment weighting (IPTW) between dupilumab and other biologics. Reductions in SA exacerbations and oral corticosteroid (OCS) prescriptions during the 12-month post-index period were estimated using a doubly robust regression. Results: A total of 2739 patients met all study criteria; 1281, 638, 406 and 414 received dupilumab, omalizumab, benralizumab and mepolizumab, respectively. After IPTW, the majority of baseline covariates were balanced (standardised difference <10%) between dupilumab and other biologics in a pairwise manner. After regression, dupilumab was associated with a lower risk of SA exacerbations during the 12-month post-index period, as follows: 22% Conclusions: The findings suggest that dupilumab may reduce severe exacerbations and OCS use in patients with SA better than omalizumab, benralizumab and mepolizumab in European real-world settings.

Identifiers

PMID40761646
PMCPMC12320101

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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.