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Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease

OBJECTIVE: It is unknown whether ustekinumab (UST) levels can predict clinical outcomes in Crohn’s disease (CD) patients. We assessed the exposure–response relationship of UST trough concentrations with biochemical outcomes at week 24 in a prospective, real-world setting. METHODS: We performed a pro...

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Autores principales: Straatmijer, Tessa, Biemans, Vince B. C., Moes, Dirk Jan A. R., Hoentjen, Frank, ter Heine, Rob, Maljaars, P. W. Jeroen, Theeuwen, Rosaline, Pierik, Marieke, Duijvestein, Marjolijn, van der Meulen-de Jong, Andrea E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188378/
https://www.ncbi.nlm.nih.gov/pubmed/36920666
http://dx.doi.org/10.1007/s10620-023-07822-7
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author Straatmijer, Tessa
Biemans, Vince B. C.
Moes, Dirk Jan A. R.
Hoentjen, Frank
ter Heine, Rob
Maljaars, P. W. Jeroen
Theeuwen, Rosaline
Pierik, Marieke
Duijvestein, Marjolijn
van der Meulen-de Jong, Andrea E.
author_facet Straatmijer, Tessa
Biemans, Vince B. C.
Moes, Dirk Jan A. R.
Hoentjen, Frank
ter Heine, Rob
Maljaars, P. W. Jeroen
Theeuwen, Rosaline
Pierik, Marieke
Duijvestein, Marjolijn
van der Meulen-de Jong, Andrea E.
author_sort Straatmijer, Tessa
collection PubMed
description OBJECTIVE: It is unknown whether ustekinumab (UST) levels can predict clinical outcomes in Crohn’s disease (CD) patients. We assessed the exposure–response relationship of UST trough concentrations with biochemical outcomes at week 24 in a prospective, real-world setting. METHODS: We performed a prospective study in patients with CD starting UST in four academic centres in the Netherlands. All patients received a weight-adjusted intravenous (IV) UST induction dose, followed by one subcutaneous (SC) dose of 90 mg UST at 8 weeks. Maintenance therapy consisted of 90 mg subcutaneous UST every 8 or 12 weeks. Individual UST concentration time course during treatment were estimated using a population pharmacokinetic (PK) model. Quartile analysis and logistic regression were performed to analyse if UST concentrations at week 8 were associated with biochemical remission rates at week 24 (C-reactive protein (CRP) ≤ 5 mg/L and / or faecal calprotectin (FC) ≤ 250 mg/kg). RESULTS: In total, 124 patients with CD were included. Patients achieving biochemical remission at week 12 and 24 had significantly higher UST levels at week 8 compared to patients without biochemical remission (6.6 µg/mL versus 3.9 µg/mL, P < 0.01 and 6.3 µg/mL versus 3.9 µg/mL, P < 0.01, respectively). In quartile analysis, patients with UST levels in the highest quartile (≥ 6.3 µg/mL at week 8) had higher biochemical remission rates at week 12 and week 24. There was no association between UST levels at and corticosteroid-free clinical remission rates. CONCLUSION: In this real-world cohort of patients with CD, UST levels in the highest quartile (≥ 6.3 µg/mL) at week 8 were associated with higher biochemical remission rates at week 24. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-023-07822-7.
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spelling pubmed-101883782023-05-18 Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease Straatmijer, Tessa Biemans, Vince B. C. Moes, Dirk Jan A. R. Hoentjen, Frank ter Heine, Rob Maljaars, P. W. Jeroen Theeuwen, Rosaline Pierik, Marieke Duijvestein, Marjolijn van der Meulen-de Jong, Andrea E. Dig Dis Sci Original Article OBJECTIVE: It is unknown whether ustekinumab (UST) levels can predict clinical outcomes in Crohn’s disease (CD) patients. We assessed the exposure–response relationship of UST trough concentrations with biochemical outcomes at week 24 in a prospective, real-world setting. METHODS: We performed a prospective study in patients with CD starting UST in four academic centres in the Netherlands. All patients received a weight-adjusted intravenous (IV) UST induction dose, followed by one subcutaneous (SC) dose of 90 mg UST at 8 weeks. Maintenance therapy consisted of 90 mg subcutaneous UST every 8 or 12 weeks. Individual UST concentration time course during treatment were estimated using a population pharmacokinetic (PK) model. Quartile analysis and logistic regression were performed to analyse if UST concentrations at week 8 were associated with biochemical remission rates at week 24 (C-reactive protein (CRP) ≤ 5 mg/L and / or faecal calprotectin (FC) ≤ 250 mg/kg). RESULTS: In total, 124 patients with CD were included. Patients achieving biochemical remission at week 12 and 24 had significantly higher UST levels at week 8 compared to patients without biochemical remission (6.6 µg/mL versus 3.9 µg/mL, P < 0.01 and 6.3 µg/mL versus 3.9 µg/mL, P < 0.01, respectively). In quartile analysis, patients with UST levels in the highest quartile (≥ 6.3 µg/mL at week 8) had higher biochemical remission rates at week 12 and week 24. There was no association between UST levels at and corticosteroid-free clinical remission rates. CONCLUSION: In this real-world cohort of patients with CD, UST levels in the highest quartile (≥ 6.3 µg/mL) at week 8 were associated with higher biochemical remission rates at week 24. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10620-023-07822-7. Springer US 2023-03-15 2023 /pmc/articles/PMC10188378/ /pubmed/36920666 http://dx.doi.org/10.1007/s10620-023-07822-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Article
Straatmijer, Tessa
Biemans, Vince B. C.
Moes, Dirk Jan A. R.
Hoentjen, Frank
ter Heine, Rob
Maljaars, P. W. Jeroen
Theeuwen, Rosaline
Pierik, Marieke
Duijvestein, Marjolijn
van der Meulen-de Jong, Andrea E.
Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title_full Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title_fullStr Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title_full_unstemmed Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title_short Ustekinumab Trough Concentrations Are Associated with Biochemical Outcomes in Patients with Crohn’s Disease
title_sort ustekinumab trough concentrations are associated with biochemical outcomes in patients with crohn’s disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10188378/
https://www.ncbi.nlm.nih.gov/pubmed/36920666
http://dx.doi.org/10.1007/s10620-023-07822-7
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