Drug treatment strategies for eosinophilic esophagitis in adults

被引:3
作者
Lucendo, Alfredo J. [1 ,2 ,3 ,4 ]
机构
[1] Hosp Gen Tomelloso, Dept Gastroenterol, Vereda Socuellamos S-N, Tomelloso 13700, Spain
[2] Inst Invest Sanitaria La Princesa, Madrid, Spain
[3] Inst Invest Sanitaria Castilla La Mancha IDISCAM, Madrid, Spain
[4] Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
关键词
Biological therapy; benralizumab; budesonide; dupilumab; cendakimab; eosinophilic esophagitis; etrasimod; food-elimination diet; fluticasone; mepolizumab; proton pump inhibitor; reslizumab; swallowed topical corticosteroids; PUMP INHIBITOR THERAPY; QUALITY-OF-LIFE; ORAL VISCOUS BUDESONIDE; SHOWS MODEST ACCURACY; JOINT TASK-FORCE; SWALLOWED FLUTICASONE; HISTOLOGIC REMISSION; TOPICAL STEROIDS; CONSENSUS RECOMMENDATIONS; GASTROESOPHAGEAL-REFLUX;
D O I
10.1080/14656566.2022.2060077
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction Eosinophilic esophagitis (EoE) is a clinical and pathological disorder, characterized by symptoms of esophageal dysfunction, and eosinophil-predominant inflammation restricted to the esophagus. Treatment outcomes include symptomatic remission, histological and endoscopic normalization and improving quality of life. Besides dietary modifications and endoscopic dilation, drugs available are swallowed topical corticosteroids (STCs) with reduced bioavailability and proton pump inhibitors (PPI). Areas covered Herein, the authors review the current treatment strategies for EoE in adults, providing the reader with their expert perspectives. The authors give discussion to the value of PPIs as a first-line therapy for EoE, in addition to the use of STCs. The current development of new formulations of STCs targeting the esophagus and novel therapies aimed at blocking molecular pathways are also discussed. Finally, the authors briefly look at the value of monoclonal antibodies targeting IL-5RA, IL-13, IL-4 or Siglec8, and oral S1PR agonists to the treatment of EoE. Expert opinion Viscose formulations of STC designed to coat the esophagus and new effervescent orodispersible tablets provide increased effectiveness at low doses. Investigational therapies that target several Th2-associated diseases seem useful in EoE. Comparative effectiveness and cost-utility analyses will help to position them in a complex therapeutic scenario.
引用
收藏
页码:827 / 840
页数:14
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