Evidence map›Paper›PMID 39694677›Full record

ArticleBMJ open respiratory research2024

What is the true target population for biologics in real-life COPD or asthma-COPD overlap patients?

Maéva Zysman, Fanchon Herman, Léo Grassion, Camille Taillé, Jesus Gonzalez-Bermejo, Marina Guecamburu, Nicolas Roche, Arthur Pavot, Pierre-Olivier Girodet, Arnaud Bourdin and 3 more

Abstract readMulticenter Study
In one paragraph

Article in BMJ open respiratory research, 2024. 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. Review
  2. Review
  3. Review
  4. Review
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

13 authors.

Maéva ZysmanCentre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, Université de Bordeaux, Bordeaux, France maeva.zysman@chu-bordeaux.fr.ORCID http://orcid.org/0000-0003-1459-2409
Fanchon HermanCHU de Montpellier, Montpellier, France.
Léo GrassionDépartement de Pneumologie, Service des Maladies Respiratoires, Hôpital du Haut Lévêque, CHU de Bordeaux, Pessac, France.ORCID http://orcid.org/0000-0002-1909-9755
Camille TailléService de Pneumologie et Centre de Référence des Maladies Pulmonaires Rares, Hôpital Bichat - Claude-Bernard, Paris, France.
Jesus Gonzalez-BermejoUMRS1158 Neurophysiologie respiratoire expérimentale et clinique, (1) Sorbonne Universités, UPMC Univ Paris 06, INSERM, Paris, France.
Marina GuecamburuDépartement de Pneumologie, Service des Maladies Respiratoires, Hôpital du Haut Lévêque, CHU de Bordeaux, Bordeaux, France.ORCID http://orcid.org/0009-0007-7719-7453
Nicolas RocheService de Pneumologie, Hôpital Cochin, AP-HP Centre, Paris, France.
Arthur PavotDépartement de Pneumologie, Service des Maladies Respiratoires, Hôpital du Haut Lévêque, CHU Bordeaux, Bordeaux, France.
Pierre-Olivier GirodetCentre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, CHU de Bordeaux, Bordeaux, France.
Arnaud BourdinClinical Research and Epidemiology Unit, CHU Montpellier, Univ Montpellier, Montpellier, France.
Nicolas MolinariClinical Research and Epidemiology Unit, CHU Montpellier, Univ Montpellier, Montpellier, France.
Patrick BergerCentre de Recherche Cardio-Thoracique de Bordeaux, U1045, CIC 1401, Université de Bordeaux, Bordeaux, France.
COBRA Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBiologics provide significant benefits in asthma, reducing exacerbations and symptoms. Some biologics have shown promising results in small subgroups of patients with chronic obstructive pulmonary disease (COPD) and frequent exacerbations. Nevertheless, real-life data on the size of the COPD target population remain scarce.

methodsWe analysed the characteristics of COPD and coexisting asthma and COPD patients included in the prospective multicentre, French COhort of BRonchial obstruction and Asthma, between 2008 and 2023 and evaluated the number of patients who could correspond to the inclusion criteria of randomised controlled trials evaluating various biologics targeting interleukin 33 (IL-33) (-receptor), IL-5 (-receptor), IL-4Rα or TSLP, in routine clinical practice.

resultsAmong 434 COPD patients, only 21.7% met inclusion criteria for at least one biologic. Among patients with asthma, 54 (3.5%) had coexisting features of COPD in terms of age, smoking status and airflow obstruction and met inclusion criteria for at least one biologic. Notably, these patients were predominantly female, with worse lung function. Globally, the target chronic airway diseases population of the eagerly awaited biologics remains limited to a small part (ie, 1.3%-8%, depending on the biologic).

conclusionIn a real-life COPD and asthma population (including asthmatic patients with features of COPD), the proportion of patients satisfying selection criteria applied in randomised controlled trials assessing the efficacy of biologics remains limited to less than 10% of the whole population.

Indexed as

Biological ProductsPulmonary Disease, Chronic ObstructiveAgedAsthmaAsthma-Chronic Obstructive Pulmonary Disease Overlap SyndromeFemaleFranceHumansMaleMiddle AgedProspective StudiesRandomized Controlled Trials as TopicBiological ProductsAsthma in primary careAsthma PharmacologyCOPD PharmacologyEosinophil Biology

Identifiers

PMID39694677
PMCPMC11667443

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Registered trials

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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.