Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
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
_version_ 1783519374619967488
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
work_keys_str_mv AT biemansvincebc ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT vandermeulendejongandreae ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT vanderwoudechristinej ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT lowenbergmark ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT dijkstragerard ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT oldenburgbas ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT deboernannekh ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT vandermarelsander ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT bodelieralexandergl ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT jansenjeroenm ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT haansjeoffreyjl ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT theeuwenrosaline ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT dejongdirk ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT pierikmariej ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy
AT hoentjenfrank ustekinumabforcrohnsdiseaseresultsoftheiccregistryanationwideprospectiveobservationalcohortstudy