Effect of Varying Doses of Epicutaneous Immunotherapy vs Placebo on Reaction to Peanut Protein Exposure Among Patients With Peanut Sensitivity: A Randomized Clinical Trial.
- 2017-11-14
- JAMA 318(18)
- Hugh A Sampson
- Wayne G Shreffler
- William H Yang
- Gordon L Sussman
- Terri F Brown-Whitehorn
- Kari C Nadeau
- Amarjit S Cheema
- Stephanie A Leonard
- Jacqueline A Pongracic
- Christine Sauvage-Delebarre
- Amal H Assa'ad
- Frederic de Blay
- J Andrew Bird
- Stephen A Tilles
- Franck Boralevi
- Thierry Bourrier
- Jacques Hébert
- Todd D Green
- Roy Gerth van Wijk
- André C Knulst
- Gisèle Kanny
- Lynda C Schneider
- Marek L Kowalski
- Christophe Dupont
- PubMed: 29136445
- DOI: 10.1001/jama.2017.16591
Study Design
- Type
- Randomized Controlled Trial (RCT)
- Sample size
- n = 221
- Population
- peanut-allergic patients (6-55 years) from 22 centers
- Methods
- Phase 2b double-blind, placebo-controlled, dose-ranging trial of a peanut patch; randomly assigned patients (1:1:1:1) received epicutaneous peanut patch containing 50 μg, 100 μg, or 250 μg of peanut protein or a placebo patch; daily patch application for 12 months
- Blinding
- Double-blind
- Duration
- 12 months
- Funding
- Unclear
- Large Human Trial
- Highly Cited
- Rigorous Journal
Importance
Epicutaneous immunotherapy may have potential for treating peanut allergy but has been assessed only in preclinical and early human trials.Objective
To determine the optimal dose, adverse events (AEs), and efficacy of a peanut patch for peanut allergy treatment.Design, setting, and participants
Phase 2b double-blind, placebo-controlled, dose-ranging trial of a peanut patch in peanut-allergic patients (6-55 years) from 22 centers, with a 2-year, open-label extension (July 31, 2012-July 31, 2014; extension completed September 29, 2016). Patients (n = 221) had peanut sensitivity and positive double-blind, placebo-controlled food challenges to an eliciting dose of 300 mg or less of peanut protein.Interventions
Randomly assigned patients (1:1:1:1) received an epicutaneous peanut patch containing 50 μg (n = 53), 100 μg (n = 56), or 250 μg (n = 56) of peanut protein or a placebo patch (n = 56). Following daily patch application for 12 months, patients underwent a double-blind, placebo-controlled food challenge to establish changes in eliciting dose.Main outcomes and measures
The primary efficacy end point was percentage of treatment responders (eliciting dose: ≥10-times increase and/or reaching ≥1000 mg of peanut protein) in each group vs placebo patch after 12 months. Secondary end points included percentage of responders by age strata and treatment-emergent adverse events (TEAEs).Results
Of 221 patients randomized (median age, 11 years [quartile 1, quartile 3: 8, 16]; 37.6% female), 93.7% completed the trial. A significant absolute difference in response rates was observed at month 12 between the 250-μg (n = 28; 50.0%) and placebo (n = 14; 25.0%) patches (difference, 25.0%; 95% CI, 7.7%-42.3%; P = .01). No significant difference was seen between the placebo patch vs the 100-μg patch. Because of statistical testing hierarchical rules, the 50-μg patch was not compared with placebo. Interaction by age group was only significant for the 250-μg patch (P = .04). In the 6- to 11-year stratum, the response rate difference between the 250-μg (n = 15; 53.6%) and placebo (n = 6; 19.4%) patches was 34.2% (95% CI, 11.1%-57.3%; P = .008); adolescents/adults showed no difference between the 250-μg (n = 13; 46.4%) and placebo (n = 8; 32.0%) patches: 14.4% (95% CI, -11.6% to 40.4%; P = .40). No dose-related serious AEs were observed. The percentage of patients with 1 or more TEAEs (largely local skin reactions) was similar across all groups in year 1: 50-μg patch = 100%, 100-μg patch = 98.2%, 250-μg patch = 100%, and placebo patch = 92.9%. The overall median adherence was 97.6% after 1 year; the dropout rate for treatment-related AEs was 0.9%.Conclusions and relevance
In this dose-ranging trial of peanut-allergic patients, the 250-μg peanut patch resulted in significant treatment response vs placebo patch following 12 months of therapy. These findings warrant a phase 3 trial.Trial registration
clinicaltrials.gov Identifier: NCT01675882.Research Insights
adolescents/adults showed no difference between the 250-μg (n = 13; 46.4%) and placebo (n = 8; 32.0%) patches: 14.4% (95% CI, -11.6% to 40.4%; P = .40).
- Effect
- Neutral
- Effect size
- Small
- Dose
- 250 μg
Adverse Events Reported
No dose-related serious AEs were observed.
- Finding
- No significant difference
- Severity
- Serious adverse event
- Significant
- No
The overall median adherence was 97.6% after 1 year; the dropout rate for treatment-related AEs was 0.9%.
- Finding
- Reported
- Magnitude
- 0.9%
The percentage of patients with 1 or more TEAEs (largely local skin reactions) was similar across all groups in year 1: 50-μg patch = 100%, 100-μg patch = 98.2%, 250-μg patch = 100%, and placebo patch = 92.9%.
- Finding
- Reported