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Relapse of Eosinophilic Esophagitis on Dupilumab

Dupilumab is approved for the treatment of eosinophilic esophagitis (EoE). We report a teenager with difficult-to-treat EoE on topical corticosteroids (TS) who achieved clinical and histological remission when initiated on dupilumab for a primary indication of atopic dermatitis. However, when his TS...

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Autores principales: Buendia, Matthew A., Choksi, Yash A., Hiremath, Girish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158342/
https://www.ncbi.nlm.nih.gov/pubmed/37168482
http://dx.doi.org/10.1097/PG9.0000000000000273
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author Buendia, Matthew A.
Choksi, Yash A.
Hiremath, Girish
author_facet Buendia, Matthew A.
Choksi, Yash A.
Hiremath, Girish
author_sort Buendia, Matthew A.
collection PubMed
description Dupilumab is approved for the treatment of eosinophilic esophagitis (EoE). We report a teenager with difficult-to-treat EoE on topical corticosteroids (TS) who achieved clinical and histological remission when initiated on dupilumab for a primary indication of atopic dermatitis. However, when his TS were weaned after achieving remission, his disease relapsed with worsening of his dysphagia and a peak eosinophilic count (PEC) of 55 eosinophils per high power field (eos/hpf). Upon restarting TS to his ongoing dupilumab, symptoms fully resolved, and he achieved histologic remission (PEC 10 eos/hpf). This report underscores the: (1) importance of longitudinal monitoring for EoE patients on dupilumab, (2) unmet need for guidance on how to transition EoE patients on traditional therapies to dupilumab, and (3) need for longitudinal follow-up data on dupilumab to help personalize therapy for EoE patients.
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spelling pubmed-101583422023-05-09 Relapse of Eosinophilic Esophagitis on Dupilumab Buendia, Matthew A. Choksi, Yash A. Hiremath, Girish JPGN Rep Case Report Dupilumab is approved for the treatment of eosinophilic esophagitis (EoE). We report a teenager with difficult-to-treat EoE on topical corticosteroids (TS) who achieved clinical and histological remission when initiated on dupilumab for a primary indication of atopic dermatitis. However, when his TS were weaned after achieving remission, his disease relapsed with worsening of his dysphagia and a peak eosinophilic count (PEC) of 55 eosinophils per high power field (eos/hpf). Upon restarting TS to his ongoing dupilumab, symptoms fully resolved, and he achieved histologic remission (PEC 10 eos/hpf). This report underscores the: (1) importance of longitudinal monitoring for EoE patients on dupilumab, (2) unmet need for guidance on how to transition EoE patients on traditional therapies to dupilumab, and (3) need for longitudinal follow-up data on dupilumab to help personalize therapy for EoE patients. Lippincott Williams & Wilkins, Inc. 2022-11-08 /pmc/articles/PMC10158342/ /pubmed/37168482 http://dx.doi.org/10.1097/PG9.0000000000000273 Text en Copyright © 2022 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and the North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Buendia, Matthew A.
Choksi, Yash A.
Hiremath, Girish
Relapse of Eosinophilic Esophagitis on Dupilumab
title Relapse of Eosinophilic Esophagitis on Dupilumab
title_full Relapse of Eosinophilic Esophagitis on Dupilumab
title_fullStr Relapse of Eosinophilic Esophagitis on Dupilumab
title_full_unstemmed Relapse of Eosinophilic Esophagitis on Dupilumab
title_short Relapse of Eosinophilic Esophagitis on Dupilumab
title_sort relapse of eosinophilic esophagitis on dupilumab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158342/
https://www.ncbi.nlm.nih.gov/pubmed/37168482
http://dx.doi.org/10.1097/PG9.0000000000000273
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