Alimentary Pharmacology & Therapeutics· 2026Q1· Clinical trial
Clinical Trial: Dupilumab Improves Eosinophilic Oesophagitis Outcomes Versus Placebo Regardless of Comorbidities or Treatment History in a Randomised Clinical Trial
- 1citations
- Q1SCImago
- 2026year
Short summary
Dupilumab significantly improved histological, symptomatic, and endoscopic outcomes in patients with eosinophilic esophagitis (EoE) compared to placebo, irrespective of patient demographics, disease characteristics, treatment history, or type 2 inflammatory comorbidities.
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Key points
- Dupilumab achieved histological remission (≤ 6 eos/hpf) in a greater proportion of EoE patients versus placebo at Week 24.
- Improvements in dysphagia symptoms (DSQ) and endoscopic scores (EREFS) were also observed with dupilumab compared to placebo.
- Efficacy of dupilumab was consistent across subgroups defined by demographics, disease duration, type 2 comorbidities, and treatment history.
- Benefits were maintained with continued dupilumab treatment through Week 52 and seen in patients switching from placebo.
AI-generated from the title and abstract; the full text is not read.
Abstract
BACKGROUND: Patients with eosinophilic oesophagitis (EoE) can present with differing disease characteristics, treatment resistance, and associated type 2 inflammatory comorbidities. We assessed the efficacy of dupilumab in subgroups of patients with EoE from the LIBERTY EoE TREET study across a range of demographics, characteristics, treatments, and comorbidities. METHODS: ), disease duration before study entry (< 5 years, ≥ 5 to < 10 years, ≥ 10 years), history of type 2 inflammatory comorbidities (with/without asthma, allergic rhinitis, atopic dermatitis, or food allergy), history of elimination diet, concurrent elimination diet, concurrent proton pump inhibitor use, and prior oesophageal dilation. Outcomes were analysed post hoc and included the proportion of patients achieving ≤ 6 eosinophils per high-power field (eos/hpf) and change from baseline in Dysphagia Symptom Questionnaire (DSQ) and total Endoscopic Reference Score (EREFS). RESULTS: At Week 24, dupilumab treatment increased the proportion of patients achieving histological remission (peak eosinophil count ≤ 6 eos/hpf) versus placebo in all subgroups. At Week 52, improvements were maintained with continued dupilumab treatment. Improvements were also observed through Week 52 in patients who switched from placebo to dupilumab at Week 24. Similar results were observed for change from baseline in DSQ and EREFS. CONCLUSIONS: Dupilumab treatment improved histological, symptomatic, and endoscopic outcomes versus placebo in patients with EoE, regardless of demographics, disease characteristics, treatment history, or type 2 inflammatory disease comorbidities. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT03633617.
The authors' abstract, as published at the source. Alimentary Pharmacology & Therapeutics, 2026 · DOI ↗
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