Rates, predictive factors and effectiveness of ustekinumab intensification to 4- or 6-weekly intervals in Crohn's disease

Dig Liver Dis. 2023 Aug;55(8):1034-1041. doi: 10.1016/j.dld.2022.10.002. Epub 2022 Oct 22.

Abstract

Background: The UNITI trial reports efficacy of ustekinumab (UST) dose intensification in Crohn's disease (CD) from 12- to 8-weekly, but not 4-weekly. We aimed 1) to assess the cumulative incidence of UST dose intensification to 4- or 6-weekly, 2) to identify factors associated with dose intensification, and 3) to assess the effectiveness of this strategy.

Methods: We performed a retrospective, observational cohort study in NHS Lothian including all UST treated CD patients (2015-2020).

Results: 163 CD patients were treated with UST (median follow-up: 20.3 months [13.4-38.4]), of whom 55 (33.7%) underwent dose intensification to 4-weekly (n = 50, 30.7%) or 6-weekly (n = 5, 3.1%). After 1 year 29.9% were dose intensified. Prior exposure to both anti-TNF and vedolizumab (HR 9.5; 1.3-70.9), and concomitant steroid use at UST start (HR 1.8; 1.0-3.1) were associated with dose intensification. Following dose intensification, 62.6% patients (29/55) remained on UST beyond 1 year. Corticosteroid-free clinical remission was achieved in 27% at week 16 and 29.6% at last follow-up.

Conclusion: One third of CD patients treated with UST underwent dose intensification to a 4- or 6-weekly interval within the first year. Patients who failed both anti-TNF and vedolizumab, or required steroids at initiation were more likely to dose intensify.

Keywords: Crohn's disease; Dose escalation; Dose optimisation; Real world evidence; Ustekinumab.

Publication types

  • Observational Study

MeSH terms

  • Adolescent
  • Adult
  • Crohn Disease* / drug therapy
  • Dermatologic Agents* / therapeutic use
  • Female
  • Humans
  • Male
  • Retrospective Studies
  • Treatment Outcome
  • Ustekinumab* / therapeutic use

Substances

  • Ustekinumab
  • Dermatologic Agents