Gastroenterology
Volume 131, Issue 5 , Pages 1381-1391 , November 2006

A Randomized, Double-Blind, Placebo-Controlled Trial of Fluticasone Propionate for Pediatric Eosinophilic Esophagitis

  • Michael R. Konikoff

      Affiliations

    • Division of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Richard J. Noel

      Affiliations

    • Division of Pediatric Gastroenterology and Nutrition, Department of Pediatrics, Children’s Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, Wisconsin
  • ,
  • Carine Blanchard

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Cassie Kirby

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Sean C. Jameson

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Bridget K. Buckmeier

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Rachel Akers

      Affiliations

    • Center for Epidemiology and Biostatistics, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Mitchell B. Cohen

      Affiliations

    • Division of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Margaret H. Collins

      Affiliations

    • Division of Pathology and Laboratory Medicine, Department of Pediatrics, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Amal H. Assa’ad

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Seema S. Aceves

      Affiliations

    • Division of Allergy and Immunology, Department of Pediatrics, Children’s Hospital of San Diego, University of California San Diego, La Jolla, California
  • ,
  • Philip E. Putnam

      Affiliations

    • Division of Pediatric Gastroenterology, Hepatology and Nutrition, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
  • ,
  • Marc E. Rothenberg

      Affiliations

    • Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio
    • Corresponding Author InformationAddress requests for reprints to: Marc E. Rothenberg, MD, PhD, Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, 3333 Burnet Avenue, ML 7028, Cincinnati, Ohio 45229-3039. fax: (513) 636-3310.

Received 12 June 2006 ,Accepted 26 July 2006.

  • Image Result

    Flow diagram of study participants.

    Flow diagram of study participants.

  • Image Result

    Percent of patients achieving response. Response (prespecified during study design) was defined as a peak eosinophil count of ≤1 eosinophil/HPF in both the proximal and distal esophagus. Response rate

    Percent of patients achieving response. Response (prespecified during study design) was defined as a peak eosinophil count of ≤1 eosinophil/HPF in both the proximal and distal esophagus. Response rates using different definitions of remissions were also calculated to determine if these influenced response rates. These included a higher peak eosinophil count (6 eosinophils/HPF), mean eosinophil count of ≤1 or ≤2, and percent reduction in peak eosinophil count from pretreatment to posttreatment (90% or 95% decrease). *P < .05.

  • Image Result
    Effect of FP therapy on esophageal eosinophil levels in the (A) proximal and (B) distal esophagus. Response to FP was nearly complete or absent; only 3 patients had intermediate eosinophil levels (bet

    Effect of FP therapy on esophageal eosinophil levels in the (A) proximal and (B) distal esophagus. Response to FP was nearly complete or absent; only 3 patients had intermediate eosinophil levels (between 1 and 24 eosinophils/HPF) after treatment with FP.

  • Image Result
    Effect of FP therapy on epithelial hyperplasia in the esophagus. On histologic examination, the thickness of the basal layer in relation to the entire epithelium was estimated in well-oriented section

    Effect of FP therapy on epithelial hyperplasia in the esophagus. On histologic examination, the thickness of the basal layer in relation to the entire epithelium was estimated in well-oriented sections, and epithelial hyperplasia was graded on a 4-point scale: no hyperplasia, basal layer occupying less than one third of the total epithelial thickness, basal layer occupying one third to two thirds of the total epithelial thickness, and basal layer occupying more than two thirds of the total epithelial thickness. Treatment with FP reduced epithelial hyperplasia in the proximal (not shown) and distal esophagus (A), while placebo had no effect. The reduction in epithelial hyperplasia was limited to FP responders (B). These results were confirmed by immunohistochemical analysis with MIB-1 in the (C) proximal and (D) distal esophagus. *P < .05, **P < .01.

  • Image Result
    Esophageal eosinophil levels by allergy status in the FP group before and after therapy. A and B represent the proximal and distal esophagus, respectively. Allergic patients were defined as those with

    Esophageal eosinophil levels by allergy status in the FP group before and after therapy. A and B represent the proximal and distal esophagus, respectively. Allergic patients were defined as those with any positive skin prick test result to food and/or environmental allergens. Only nonallergic patients showed a significant decrease in esophageal eosinophil levels with FP treatment. This effect was more pronounced in the proximal esophagus. *P < .05.

  • Image Result
    Effect of patient characteristics on response to FP. FP responders were significantly (A) younger, (C) shorter, and (E) lighter in weight than nonresponders. (B) Age, (D) height, and (F) weight signif

    Effect of patient characteristics on response to FP. FP responders were significantly (A) younger, (C) shorter, and (E) lighter in weight than nonresponders. (B) Age, (D) height, and (F) weight significantly correlated with eosinophil levels in the distal esophagus after treatment with FP. *P < .05, **P < .01, ***P < .001.

  • Image Result
    Immunopathologic effects of FP on the esophagus. Treatment with FP decreased esophageal CD8+ T cell counts in both the proximal (not shown) and (A) distal esophagus, but this decrease was limited to F

    Immunopathologic effects of FP on the esophagus. Treatment with FP decreased esophageal CD8+ T cell counts in both the proximal (not shown) and (A) distal esophagus, but this decrease was limited to FP responders. Treatment with FP also decreased esophageal mast cell counts in both the proximal (not shown) and (B) distal esophagus, but this decrease was limited to FP responders. FP responders had lower posttreatment levels of mast cells than FP nonresponders. *P < .05, **P < .01.

 Supported by the Burroughs Wellcome Fund, the CURED Foundation, the Buckeye Foundation, an American Academy of Allergy Asthma & Immunology/Sanofi-Aventis Women Physician in Allergy grant, and a grant from the US Public Health Service (NIH T32 DK007727).

PII: S0016-5085(06)01792-6

doi: 10.1053/j.gastro.2006.08.033

Gastroenterology
Volume 131, Issue 5 , Pages 1381-1391 , November 2006