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Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study
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...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142409/ https://www.ncbi.nlm.nih.gov/pubmed/31219157 http://dx.doi.org/10.1093/ecco-jcc/jjz119 |
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author | 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 |
author_facet | 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 |
author_sort | Biemans, Vince B C |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-7142409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71424092020-04-13 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 J Crohns Colitis Original Articles 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. Oxford University Press 2020-01 2019-06-14 /pmc/articles/PMC7142409/ /pubmed/31219157 http://dx.doi.org/10.1093/ecco-jcc/jjz119 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of European Crohn’s and Colitis Organisation. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Articles 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 Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title | Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title_full | Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title_fullStr | Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title_full_unstemmed | Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title_short | Ustekinumab for Crohn’s Disease: Results of the ICC Registry, a Nationwide Prospective Observational Cohort Study |
title_sort | ustekinumab for crohn’s disease: results of the icc registry, a nationwide prospective observational cohort study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7142409/ https://www.ncbi.nlm.nih.gov/pubmed/31219157 http://dx.doi.org/10.1093/ecco-jcc/jjz119 |
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