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Early azathioprine therapy is no more effective than placebo for newly diagnosed Crohn's disease
Julián Panés1, Antonio López-Sanromán, Fernando Bermejo
1Hospital Clínic/IDIBAPS, Barcelona, Spain; Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas y Digestivas, Barcelona, Spain.
Insights
Early azathioprine therapy in adults with Crohn's disease did not improve sustained corticosteroid-free remission compared to placebo. However, it showed potential in preventing moderate to severe relapse in a post hoc analysis.
Area of Science:
- Gastroenterology
- Clinical Pharmacology
- Immunosuppressive Therapy
Background:
- Limited data exists on early thiopurine therapy efficacy in adult Crohn's disease.
- Previous studies focused on mercaptopurine in pediatric Crohn's disease.
Purpose of the Study:
- To evaluate the efficacy of early azathioprine therapy in adults with newly diagnosed Crohn's disease.
- To assess sustained corticosteroid-free remission as the primary outcome.
Main Methods:
- Prospective, double-blind, placebo-controlled trial.
- Adults with recent Crohn's disease diagnosis randomly assigned to azathioprine or placebo.
- Primary efficacy measure: sustained corticosteroid-free remission at 76 weeks.
Main Results:
- No significant difference in sustained corticosteroid-free remission between azathioprine and placebo groups (44.1% vs 36.5%).
- Similar rates of relapse and corticosteroid requirements between groups.
- Post hoc analysis indicated lower relapse rates (CDAI > 220) with azathioprine (11.8% vs 30.2%).
- Higher incidence of adverse events leading to discontinuation in the azathioprine group.
Conclusions:
- Early azathioprine therapy is not superior to placebo for achieving sustained corticosteroid-free remission in adult Crohn's disease.
- Azathioprine may help prevent moderate to severe relapse, requiring further investigation.
- Increased adverse events necessitate careful monitoring of azathioprine therapy.
Background & Aims:
A small placebo-controlled trial reported the efficacy of mercaptopurine therapy for children newly diagnosed with Crohn's disease, yet little is known about the efficacy of early thiopurine therapy in adults.
Methods:
We performed a prospective double-blind trial of adult patients with a recent (<8 weeks) diagnosis of Crohn's disease. Patients were randomly assigned to groups given azathioprine (2.5 mg · kg(-1) · day(-1), n = 68) or placebo (n = 63) at 31 hospitals from February 2006 to September 2009. Corticosteroids but no other concomitant medications were allowed for control of disease activity. The primary measure of efficacy was sustained corticosteroid-free remission.
Results:
After 76 weeks of treatment, 30 patients treated with azathioprine (44.1%) and 23 given placebo (36.5%) were in sustained corticosteroid-free remission (difference of 7.6%; 95% confidence interval, -9.2 to 24.4%; P = .48). The rates of relapse (defined as Crohn's Disease Activity Index score >175) and corticosteroid requirements were similar between groups. A post hoc analysis of relapse, defined as a Crohn's Disease Activity Index score >220, showed lower relapse rates in the azathioprine group than in the placebo group (11.8% vs 30.2%; P = .01). Serious adverse events occurred in 14 patients in the azathioprine group (20.6%) and 7 in the placebo group (11.1%) (P = .16). A larger percentage of patients in the azathioprine group had adverse events that led to study drug discontinuation (20.6%) than in the placebo group (6.35%) (P = .02).
Conclusions:
In a study of adults with Crohn's disease, early azathioprine therapy was no more effective than placebo to achieve sustained corticosteroid-free remission but was more effective in preventing moderate to severe relapse in a post hoc analysis. EudraCT 2005-001186-34.
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