Oral Viscous Budesonide in Children With Eosinophilic Esophagitis After Repaired Esophageal Atresia: A Clinical Trial

Author:

Tambucci Renato1,Roversi Marco2,Rea Francesca1,Malamisura Monica1,Angelino Giulia1,Biondi Isabella3,Simeoli Raffaele4,Goffredo Bianca Maria4,Francalanci Paola1,Simonetti Alessandra3,Livadiotti Susanna3,Corsetti Tiziana5,Dall’Oglio Luigi6,Rossi Paolo3,Pontrelli Giuseppe3,De Angelis Paola1

Affiliation:

1. Digestive Endoscopy Unit, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

2. Residency School of Pediatrics, University of Rome Tor Vergata, Rome, Italy

3. Centre of Excellence for the Development and Implementation of Medicines, Vaccines, and Medical Devices for Pediatric Use, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

4. Division of Metabolic Diseases and Drug Biology, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

5. Unit of Clinical Pharmacy, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy

6. Digestive Endoscopy and Surgery Unit, Bambino Gesù Children’s Hospital IRCCS, Rome, Italy.

Abstract

Objectives: A high prevalence of eosinophilic esophagitis (EoE) has been reported in children with repaired esophageal atresia (EA). Topical steroids proved to be an effective and safe therapy in EoE, although not approved in pediatrics. We report the results of the first clinical trial of oral viscous budesonide (OVB) performed in children with EoE after repaired esophageal atresia (EoE-EA). Methods: This open-label, single-arm, phase 2 clinical trial with randomized pharmacokinetic sampling, was conducted at the Bambino Gesù Children’s Hospital between September 2019 and June 2021. EoE-EA patients received an age-banded dose of OVB twice daily for 12 weeks and were endoscopically evaluated. The primary endpoint was the rate of patients achieving histological remission. Secondary endpoints included clinical and endoscopic benefit after treatment, and safety assessments. Results: Eight consecutive EA-EoE patients were enrolled (median age 9.1 years, interquartile range 5.5). Of these, 5 received 0.8 mg and 3 received 1.0 mg twice daily of OVB. Histological remission was obtained in all but 1 patient (87.5%). The clinical score showed significant improvement at the end of treatment in all patients. No endoscopic features of EoE were found after treatment. No treatment-emergent adverse event occurred. Conclusion: OVB is an effective, safe, and well-tolerated formulation of budesonide for use in pediatric patients with EoE-EA.

Publisher

Wiley

Subject

Gastroenterology,Pediatrics, Perinatology and Child Health

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