Montelukast Does not Maintain Symptom Remission After Topical Steroid Therapy for Eosinophilic Esophagitis

Clin Gastroenterol Hepatol. 2017 Feb;15(2):214-221.e2. doi: 10.1016/j.cgh.2016.09.013. Epub 2016 Sep 17.

Abstract

Background & aims: Montelukast, a cysteinyl leukotriene type-1 receptor blocker, has been shown in small retrospective studies to reduce symptoms in patients with eosinophilic esophagitis (EoE). We performed a randomized, placebo-controlled, double-blind trial to determine whether montelukast maintains symptomatic remission induced by topical steroid therapy in patients with EoE.

Methods: We performed a prospective study of adult patients with EoE (solid-food dysphagia and a peak esophageal eosinophil count of >20 cells/high-powered field) enrolled at the Mayo Clinic in Rochester, Minnesota, from April 2008 through February 2015. All patients had been treated previously for at least 6 weeks with a topical steroid until their symptoms were in remission. Steroids were discontinued and patients then were assigned randomly to groups given montelukast (20 mg/day, n = 20) or placebo (n = 21) for 26 weeks (groups were matched for age, sex, history of allergic disease, reflux symptoms, and endoscopic findings of EoE). Study participants were assessed via a structured telephone interview at weeks 2, 4, 8, 12, 16, 20, and 24. Remission was defined as the absence of solid-food dysphagia.

Results: Based on an intention-to-treat analysis, after 26 weeks, 40.0% of subjects in the montelukast group and 23.8% in the placebo group were in remission. The odds ratio for remission in the montelukast group was 0.48 (95% confidence interval, 0.10-2.16) (P = .33). No side effects were reported from either group.

Conclusions: In a randomized controlled trial of the ability of montelukast to maintain remission in patients in remission from EoE after steroid therapy, we found montelukast to be well tolerated; 40% of patients remained in remission, but this proportion did not differ significantly from that of the placebo group. ClinicalTrials.gov no: NCT00511316.

Keywords: Clinical Trial; Drug; Inflammation; Swallow; Treatment.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Acetates / adverse effects
  • Acetates / therapeutic use*
  • Adolescent
  • Adult
  • Aged
  • Cyclopropanes
  • Cytochrome P-450 CYP1A2 Inducers
  • Double-Blind Method
  • Eosinophilic Esophagitis / drug therapy*
  • Female
  • Humans
  • Leukotriene Antagonists / adverse effects
  • Leukotriene Antagonists / therapeutic use*
  • Maintenance Chemotherapy / adverse effects
  • Maintenance Chemotherapy / methods*
  • Male
  • Middle Aged
  • Minnesota
  • Placebos / administration & dosage
  • Prospective Studies
  • Quinolines / adverse effects
  • Quinolines / therapeutic use*
  • Steroids
  • Sulfides
  • Treatment Outcome
  • Young Adult

Substances

  • Acetates
  • Cyclopropanes
  • Cytochrome P-450 CYP1A2 Inducers
  • Leukotriene Antagonists
  • Placebos
  • Quinolines
  • Steroids
  • Sulfides
  • montelukast

Associated data

  • ClinicalTrials.gov/NCT00511316