Network meta-analysis: efficacy and safety of treatments for fistulising Crohn's disease

Eur J Gastroenterol Hepatol. 2023 Jul 1;35(7):702-710. doi: 10.1097/MEG.0000000000002552. Epub 2023 Apr 10.

Abstract

Introduction: Fistulas are a debilitating complication of Crohn's disease and treatment options remain limited. There is a lack of head-to-head comparisons between treatments. To our knowledge, this is the first network meta-analysis on the efficacy of medical therapies in achieving fistula remission and maintenance of fistula closure in Crohn's disease.

Methods: Biomedical databases and the Cochrane Central Registry were searched between 1978 and 2022 for randomized controlled trials (RCTs) reporting on treatments. A network meta-analysis was performed using the frequentist model with pooled relative risks (RRs) and P -scores used to rank treatments.

Results: Twenty-five RCTs were included for analysis with 2239 patients included. At the 16-24 week time point, infliximab produced the only statistically significant result with the 5 mg/kg dose proving the most effective [RR, 2.30; 95% confidence interval (CI), 1.40-3.77]. At 44 weeks, ustekinumab was found to be most superior with it being 2.38 times (RR, 2.38; 95% CI, 1.24-4.56) more superior to placebo, with adalimumab (RR, 2.06; 95% CI, 1.06-3.99) and infliximab 5 mg/kg (RR, 1.68; 95% CI, 1.03-2.75) also producing a statistically significant result.

Conclusion: Despite infliximab being favoured in international guidelines for the treatment of perianal fistulising Crohn's disease, biologics such as ustekinumab, vedolizumab and adalimumab show promising results.

Publication types

  • Meta-Analysis

MeSH terms

  • Adalimumab / adverse effects
  • Antibodies, Monoclonal / adverse effects
  • Crohn Disease* / complications
  • Crohn Disease* / drug therapy
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Infliximab / adverse effects
  • Ustekinumab / adverse effects

Substances

  • Adalimumab
  • Antibodies, Monoclonal
  • Immunosuppressive Agents
  • Infliximab
  • Ustekinumab