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Ustekinumab for Crohn's Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study.
Biemans, Vince B C; van der Meulen-de Jong, Andrea E; van der Woude, Christine J; Löwenberg, Mark; Dijkstra, Gerard; Oldenburg, Bas; de Boer, Nanne K H; van der Marel, Sander; Bodelier, Alexander G L; Jansen, Jeroen M; Haans, Jeoffrey J L; Theeuwen, Rosaline; de Jong, Dirk; Pierik, Marie J; Hoentjen, Frank.
Afiliación
  • Biemans VBC; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • van der Meulen-de Jong AE; Department of Gastroenterology and Hepatology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • van der Woude CJ; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Löwenberg M; Department of Gastroenterology and Hepatology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Dijkstra G; Department of Gastroenterology and Hepatology, Amsterdam University Medical Centre, Academic Medical Centre, Amsterdam, The Netherlands.
  • Oldenburg B; Department of Gastroenterology and Hepatology, University Medical Centre Groningen, Groningen, The Netherlands.
  • de Boer NKH; Department of Gastroenterology and Hepatology, University Medical Centre Utrecht, Utrecht, The Netherlands.
  • van der Marel S; Department of Gastroenterology and Hepatology, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, Amsterdam, Gastroenterology and Metabolism Research Institute, Amsterdam, The Netherlands.
  • Bodelier AGL; Department of Gastroenterology and Hepatology, Haaglanden Medical Centre, the Hague, The Netherlands.
  • Jansen JM; Department of Gastroenterology and Hepatology, Amphia Hospital, Breda, The Netherlands.
  • Haans JJL; Department of Gastroenterology and Hepatology, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
  • Theeuwen R; Department of Gastroenterology and Hepatology, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • de Jong D; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Pierik MJ; Department of Gastroenterology and Hepatology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Hoentjen F; Department of Gastroenterology and Hepatology, Maastricht University Medical Centre, Maastricht, The Netherlands.
J Crohns Colitis ; 14(1): 33-45, 2020 Jan 01.
Article en En | MEDLINE | ID: mdl-31219157
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Crohn / Ustekinumab Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad de Crohn / Ustekinumab Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: J Crohns Colitis Asunto de la revista: GASTROENTEROLOGIA Año: 2020 Tipo del documento: Article País de afiliación: Países Bajos Pais de publicación: Reino Unido