Evidence map›Paper›PMID 42099297›Full record

ArticleClinical case reports2026

Less Can Be Enough: Sustained Remission of Pediatric Eosinophilic Esophagitis With Low-Frequency Dupilumab.

Giovanni Scatigna, Annarita Iadecola, Martina Piersanti, Giovanni Di Nardo, Maurizio Mennini

Abstract read
In one paragraph

Article in Clinical case reports, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Giovanni ScatignaNESMOS Department, Faculty of Medicine and Psychology Sapienza University of Rome, Pediatric Unit, Sant'Andrea University Hospital Rome Italy.
Annarita IadecolaNESMOS Department, Faculty of Medicine and Psychology Sapienza University of Rome, Pediatric Unit, Sant'Andrea University Hospital Rome Italy.
Martina PiersantiNESMOS Department, Faculty of Medicine and Psychology Sapienza University of Rome, Pediatric Unit, Sant'Andrea University Hospital Rome Italy.
Giovanni Di NardoNESMOS Department, Faculty of Medicine and Psychology Sapienza University of Rome, Pediatric Unit, Sant'Andrea University Hospital Rome Italy.
Maurizio MenniniNESMOS Department, Faculty of Medicine and Psychology Sapienza University of Rome, Pediatric Unit, Sant'Andrea University Hospital Rome Italy.ORCID https://orcid.org/0000-0003-4000-6004

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Eosinophilic esophagitis (EoE) is a chronic, immune-mediated disease requiring long-term therapy. Dupilumab, an interleukin-4 and interleukin-13 receptor antagonist, is approved for EoE at a weekly 300 mg dosing regimen. However, data on reduced-frequency dosing, especially in pediatric patients, remain limited. This is the case of a 12-year-old girl presented with vomiting, food impaction, and dysphagia. Endoscopy revealed longitudinal furrows and whitish exudates (EREFS 4), and histology confirmed EoE with 75 eosinophils/high-power field (HPF) and high EoEHSS grade and stage scores. Conventional therapies with proton pump inhibitors, topical fluticasone, and an elimination diet achieved only partial improvement. Dupilumab (300 mg every 2 weeks) induced complete clinical, endoscopic (EREFS 0), and histologic remission (EoEHSS grade/stage 0-1, peak < 6 eos/HPF) after 6 months. Given the remission and parental concern about prolonged therapy, the dosing interval was cautiously extended to every 3 weeks as a monitored off-label trial. Topical steroids and dietary restrictions were discontinued. The patient remained asymptomatic and in complete histologic remission for more than 2 years (as of August 2025: EREFS 0, EoEHSS 0, with a peak eosinophil count of ≤ 6 eos/HPF) without any adverse events. This case illustrates that sustained remission of pediatric EoE may be achievable with individualized, response-based dupilumab de-escalation. While promising, this off-label approach requires confirmation in prospective studies before routine implementation.

Indexed as

dupilumabeosinophilic esophagitislow‐frequency dosingpediatricprecision medicine

Identifiers

PMID42099297
PMCPMC13147150

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