Evidence map›Paper›PMID 40483369›Full record

ArticlePediatric research2025

A nationwide experience of biological treatments in children with eosinophilic esophagitis.

Juliette Soudant, Stéphanie Lejeune, Madeleine Aumar, Nicolas Caron, Hélène Lengline, Cyrille Hoarau, Nicolas Kalach, Raphaël Enaud, Marjorie Bonneton, Claire Dupont-Lucas and 9 more

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Article in Pediatric research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Juliette SoudantUniv.Lille, CHU Lille, Pediatric Gastroenterology Hepatology and Nutrition Department, Jeanne de Flandre Hospital, CHU Lille, F-59000, Lille, France.
Stéphanie LejeuneUniv. Lille, CHU Lille, Pediatric Pulmonology and Allergy Department, Jeanne de Flandre Hospital, CHU Lille, F-59000, Lille, France.
Madeleine AumarUniv.Lille, CHU Lille, Pediatric Gastroenterology Hepatology and Nutrition Department, Jeanne de Flandre Hospital, CHU Lille, F-59000, Lille, France.
Nicolas CaronHCL, Hôpital Femme-Mère-Enfant CHU de Lyon, Bron, 69500, France.
Hélène LenglineDepartment of Pediatric Gastroenterology and Nutrition, Robert-Debré University Hospital, APHP, Paris, France.
Cyrille HoarauCEREMAST, Service d'Immunologie Clinique et d'Allergologie, Centre Hospitalier Régional Universitaire, Tours, France.
Nicolas KalachDepartment of Paediatrics, Saint Antoine Paediatric Hospital, Saint Vincent de Paul Hospital, Groupement des Hôpitaux de l'Institut Catholique de Lille, Catholic University of Lille, Lille, France.
Raphaël EnaudDepartment of Pediatric Gastroenterology and Hepatology, University Hospital, Bordeaux, France.
Marjorie BonnetonDepartment of Pediatric Gastroenterology, Hepatology and Nutrition, Children's Hospital, Vandoeuvre-lès-Nancy, France.
Claire Dupont-LucasDepartment of Pediatric Gastroenterology, University Hospital, Caen, France.
Alexandre FabrePediatric Multidisciplinary Department, Timone Enfant Hospital, Assistance Publique-Hôpitaux de Marseille, INSERM, MMG, U1251, Aix Marseille Univ, Marseille, France.
Mathilde ButoriPediatric Gastroenterology Department, Hôpitaux pédiatriques de Nice CHU-Lenval, Nice, France.
Anaïs LemoinePediatric Nutrition and Gastroenterology, Trousseau Hospital, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, F-75012, Paris, France.
Laure Bridoux-HennoDepartment of Pediatrics, Hôpital Sud, University Hospital Rennes, Rennes, France.
Julie RebeuhDepartment of Pediatrics, University Hospital, Strasbourg, France.
Georges DimitrovPaediatrics, Centre Hospitalier Régional d'Orléans, Orleans, France.
Émeline CaillauBiostatistics Department, CHU Lille, 59000, Lille, France.
Frédéric GottrandUniv.Lille, CHU Lille, Pediatric Gastroenterology Hepatology and Nutrition Department, Jeanne de Flandre Hospital, CHU Lille, F-59000, Lille, France.
Léa Chantal TranUniv.Lille, CHU Lille, Pediatric Gastroenterology Hepatology and Nutrition Department, Jeanne de Flandre Hospital, CHU Lille, F-59000, Lille, France. lea.tran@chu-lille.fr.ORCID http://orcid.org/0000-0002-7574-7956

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNo biological treatment has been approved for pediatric eosinophilic esophagitis (EoE) in France. For patients refractory to conventional treatments, although compassionate use of monoclonal antibodies has developed, experience remains limited.

methodsWe conducted a national multicenter study across French pediatric tertiary care centers where children (younger than 18 years) who presented with EoE were treated with biological therapies between January 2015 and December 2023. The main objective was to characterize this patient population, and the indications for prescribing biologics. The secondary goals were to assess these patients' clinical, endoscopic, and histologic finding, as well as patient tolerance, and to compare our cohort at baseline with pediatric patients from two European registers of EoE treated with conventional therapies.

resultsThirty-six patients were prescribed 37 biologics (omalizumab, n = 1; mepolizumab, n = 6; dupilumab, n = 30). At diagnosis, the mean patient age was 7.4 (±4.4) years, and most patients had at least one atopic comorbidity (91.7%, n = 33). Failure of first-line treatments was the main reason for starting biological therapy (75.7%, n = 28), prescribed as compassionate use (54.1%, n = 20). Dupilumab showed significant clinical (48%, p < 0.01) and histological (82.6%, p < 0.01) improvement. Compared with children treated with conventional therapies, patients in our cohort at baseline presented significantly more asthma, food allergies, and atopic dermatitis, as well as more fibrostenotic phenotype and digestive symptoms. No severe side effect was reported within a 6-12-month follow-up.

conclusionDupilumab is the most frequently prescribed, and appears to be the most effective biotherapy, regarding clinical and histologic remission. All biologics were well-tolerated. IMPACT: Pending marketing authorization, biological therapies for pediatric eosinophilic esophagitis are mainly prescribed after failure of first-line treatments and on a compassionate basis in France. Dupilumab is the biotherapy most frequently used, is associated with clinical and histological efficacy and is well-tolerated. Children and adolescents requiring biologics appear to be younger and more severe at diagnosis than naive pediatric patients in Europeans registries.

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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.