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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.
Afiliação
  • Straatmijer T; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • Biemans VBC; Division Gastroenterology-Hepatology, Maastricht University Medical Center+, Maastricht, The Netherlands.
  • Moes DJAR; UMC Utrecht, Utrecht, The Netherlands.
  • Hoentjen F; Department of Clinical Pharmacy and Toxicology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Ter Heine R; Division of Gastroenterology, University of Alberta, Edmonton, Canada.
  • Maljaars PWJ; Department of Gastroenterology, Radboud University Medical Centre, Nijmegen, The Netherlands.
  • Theeuwen R; Department of Pharmacy, Radboud Institute for Heulth Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Pierik M; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • Duijvestein M; Department of Gastroenterology and Hepatology, Leiden University Medical Centre, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.
  • van der Meulen-de Jong AE; MUMC+, Maastricht, the Netherlands.
Dig Dis Sci ; 68(6): 2647-2657, 2023 06.
Article em En | MEDLINE | ID: mdl-36920666
ABSTRACT

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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Crohn / Ustekinumab Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Crohn / Ustekinumab Idioma: En Ano de publicação: 2023 Tipo de documento: Article