TY - JOUR
T1 - Disease Burden and Unmet Need in Eosinophilic Esophagitis
AU - Bredenoord, Albert J.
AU - Patel, Kiran
AU - Schoepfer, Alain M.
AU - Dellon, Evan S.
AU - Chehade, Mirna
AU - Aceves, Seema S.
AU - Spergel, Jonathan M.
AU - Shumel, Brad
AU - Deniz, Yamo
AU - Rowe, Paul J.
AU - Jacob-Nara, Juby A.
N1 - Funding Information:
Potential competing interests: A.J.B. received consulting fees from Arena Pharmaceuticals, AstraZeneca, Calypso Biotech, Dr. Falk Pharma, EsoCap, Gossamer Bio, Laborie, Medtronic, RB Pharma, Regeneron Pharmaceuticals, Inc./Sanofi, and Robarts Clinical Trials; research funding from Bayer, Nutricia, and SST; and holds equity interest in SST. A.M.S. received consulting fees from Adare Pharma Solutions, Bristol Myers Squibb, Dr. Falk Pharma, Ellodi Pharmaceuticals, Gossamer Bio, and Sanofi Genzyme and research funding from AstraZeneca, Aptalis, Dr. Falk Pharma, GlaxoSmithKline, Nestlé, Novartis, Receptos/Bristol Myers Squibb, and Regeneron Pharmaceuticals, Inc. E.S.D. received consulting fees from Abbott, AbbVie, Adare Pharma Solutions/Ellodi Pharmaceuticals, Aimmune Therapeutics, Allakos, Amgen, Arena Pharmaceuticals, AstraZeneca, Avir Pharma, Biorasi, Calypso Biotech, Celldex Therapeutics, Eli Lilly, EsoCap, GlaxoSmithKline, Gossamer Bio, Landos Biopharma, Morphic Therapeutic, Nutricia, Parexel/Calyx, Phathom Pharmaceuticals, Receptos/Bristol Myers Squibb, Regeneron Pharmaceuticals Inc., Revolo Biotherapeutics, Robarts Clinical Trials/Alimentiv, Salix Pharmaceuticals, Sanofi, and Shire/Takeda; research funding from Adare Pharma Solutions/Ellodi Pharmaceuticals, Allakos, Arena Pharmaceuticals, AstraZeneca, GlaxoSmithKline, Meritage Pharma, Miraca Life Sciences, Nutricia, Receptos/Bristol Myers Squibb, Regeneron Pharmaceuticals, Inc., and Shire/Takada; and educational grants from Allakos, Banner Pharmaceuticals, and Holoclara. S.S.A. received consulting fees from AstraZeneca, is an educational speaker for Sanofi-Regeneron Pharmaceuticals, Inc., and Medscape, and is a coinventor of oral viscous budesonide, UCSD patent, Takeda license. M.C. received consulting fees from Adare Pharma Solutions, Allakos, AstraZeneca, Bristol Myers Squibb, Phathom Pharmaceuticals, Regeneron Pharmaceuticals, Inc., Sanofi, and Shire/Takeda and research funding from Adare Pharma Solutions/Ellodi Pharmaceuticals, Allakos, AstraZeneca, Danone, Regeneron Pharmaceuticals Inc., and Shire. J.M.S. received consulting fees from Allakos, DBV Technologies, Novartis, Regeneron Pharmaceuticals, Inc., Shire, and Takeda and grant support from DBV Technologies and Regeneron Pharmaceuticals, Inc. B.S., and Y.D. are employees and shareholders of Regeneron Pharmaceuticals, Inc. J.A.J.-N, P.J.R., and K.P. are employees of Sanofi and may hold stock and/or stock options in the company. ACKNOWLEDGEMENTS
Publisher Copyright:
© 2022 Wolters Kluwer Health. All rights reserved.
PY - 2022/8/1
Y1 - 2022/8/1
N2 - Eosinophilic esophagitis (EoE) is a chronic, progressive, type 2 inflammatory disease of increasing prevalence, characterized by symptoms of dysphagia and reduced quality of life. A dysregulated type 2 immune response to food and aeroallergen leads to barrier dysfunction, chronic esophageal inflammation, remodeling, and fibrosis. Patients with EoE have impaired quality of life because of dysphagia and other symptoms. They may also suffer social and psychological implications of food-related illness and expensive out-of-pocket costs associated with treatment. Disease burden in EoE is often compounded by the presence of comorbid type 2 inflammatory diseases. Current conventional treatments include elimination diet, proton pump inhibitors, and swallowed topical corticosteroids, as well as esophageal dilation in patients who have developed strictures. These treatments demonstrate variable response rates and may not always provide long-term disease control. There is an unmet need for long-term histologic, endoscopic, and symptomatic disease control; for targeted therapies that can normalize the immune response to triggers, reduce chronic inflammation, and limit or prevent remodeling and fibrosis; and for earlier diagnosis, defined treatment outcomes, and a greater understanding of patient perspectives on treatment. In addition, healthcare professionals need a better understanding of the patient perspective on disease burden, the disconnect between symptoms and disease activity, and the progressive nature of EoE and the need for continuous monitoring and maintenance treatment. In this review, we explore the progression of disease over the patient's lifespan, highlight the patient perspective on disease, and discuss the unmet need for effective long-term treatments.
AB - Eosinophilic esophagitis (EoE) is a chronic, progressive, type 2 inflammatory disease of increasing prevalence, characterized by symptoms of dysphagia and reduced quality of life. A dysregulated type 2 immune response to food and aeroallergen leads to barrier dysfunction, chronic esophageal inflammation, remodeling, and fibrosis. Patients with EoE have impaired quality of life because of dysphagia and other symptoms. They may also suffer social and psychological implications of food-related illness and expensive out-of-pocket costs associated with treatment. Disease burden in EoE is often compounded by the presence of comorbid type 2 inflammatory diseases. Current conventional treatments include elimination diet, proton pump inhibitors, and swallowed topical corticosteroids, as well as esophageal dilation in patients who have developed strictures. These treatments demonstrate variable response rates and may not always provide long-term disease control. There is an unmet need for long-term histologic, endoscopic, and symptomatic disease control; for targeted therapies that can normalize the immune response to triggers, reduce chronic inflammation, and limit or prevent remodeling and fibrosis; and for earlier diagnosis, defined treatment outcomes, and a greater understanding of patient perspectives on treatment. In addition, healthcare professionals need a better understanding of the patient perspective on disease burden, the disconnect between symptoms and disease activity, and the progressive nature of EoE and the need for continuous monitoring and maintenance treatment. In this review, we explore the progression of disease over the patient's lifespan, highlight the patient perspective on disease, and discuss the unmet need for effective long-term treatments.
UR - http://www.scopus.com/inward/record.url?scp=85135597644&partnerID=8YFLogxK
U2 - 10.14309/ajg.0000000000001777
DO - 10.14309/ajg.0000000000001777
M3 - Review article
C2 - 35417421
AN - SCOPUS:85135597644
SN - 0002-9270
VL - 117
SP - 1231
EP - 1241
JO - American Journal of Gastroenterology
JF - American Journal of Gastroenterology
IS - 8
ER -