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Ustekinumab for Crohn's Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study

  • V.B.C. Biemans
  • , A.E. van der Meulen-de Jong
  • , C.J. van der Woude
  • , M. Lowenberg
  • , G. Dijkstra
  • , B. Oldenburg
  • , N.K.H. de Boer
  • , S. van der Marel
  • , A.G.L. Bodelier
  • , J.M. Jansen
  • , J.J.L. Haans
  • , R. Theeuwen
  • , D. de Jong
  • , M.J. Pierik
  • , F. Hoentjen*
  • , Dutch Initiative Crohn and Colitis
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background and Aims: Ustekinumab is approved for the treatment of Crohn's disease [CD]. Systematically registered prospective real-world data are scarce. We therefore aimed to study the effectiveness, safety and usage of ustekinumab for CD in everyday practice.Methods: We prospectively enrolled CD patients initiating ustekinumab in regular care between December 2016 and January 2019. Clinical (Harvey Bradshaw Index [HBI]), biochemical (C-reactive protein [CRP] and faecal calprotectin [FCP]), extra-intestinal manifestations and, peri-anal fistula activity, ustekinumab dosage, concomitant medication use, and adverse events were documented at weeks 0, 12, 24, and 52.The primary outcome was corticosteroid-free clinical remission.Results: In total, 221 CD patients were included (98.6% anti-tumour necrosis factor [TNF] and 46.6% vedolizumab exposed) with a median follow-up of 52.0 weeks [interquartile range 49.3-58.4]. Corticosteroid-free clinical remission rates at weeks 24 and 52 were 38.2% and 37.1%, respectively. An initial dosing schedule of 8 weeks, compared to 12 weeks, correlated with a lower discontinuation rate [20.0% vs 42.6%, p = 0.01], but comparable corticosteroid-free clinical remission at week 52 (46.3% [q8w] vs 34.6% [q12w], p = 0.20). There was no clinical benefit of combination therapy after 52 weeks when compared to ustekinumab monotherapy [combi 40.6% vs mono 36.0%, p = 0.64]. At baseline, 28 patients had active peri-anal fistula, of whom 35.7% showed complete clinical resolution after 24 weeks. During follow-up we encountered six severe infections [3.5 per 100 patient-years], with all patients being on concomitant immunosuppressant therapies. Ustekinumab treatment discontinuation was observed in 75 [33.9%] patients mainly due to lack of response.Conclusion: Ustekinumab is a relatively safe and effective treatment option for CD patients with prior failure of anti-TNF and anti-integrin therapies.
Original languageEnglish
Pages (from-to)33-45
Number of pages13
JournalJournal of Crohn's & Colitis
Volume14
Issue number1
DOIs
Publication statusPublished - 1 Jan 2020

Keywords

  • anti-tnf
  • crohn's disease
  • efficacy
  • icc registry
  • induction
  • inflammatory-bowel-disease
  • maintenance therapy
  • outcomes
  • real-world experience
  • subcutaneous ustekinumab
  • ustekinumab
  • ANTI-TNF
  • EFFICACY
  • Ustekinumab
  • Crohn's disease
  • INDUCTION
  • MAINTENANCE THERAPY
  • INFLAMMATORY-BOWEL-DISEASE
  • SUBCUTANEOUS USTEKINUMAB
  • ICC Registry
  • OUTCOMES
  • REAL-WORLD EXPERIENCE

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