4.5 Article

Clinical efficacy, drug sustainability and serum drug levels in Crohn's disease patients treated with ustekinumab - A prospective, multicenter cohort from Hungary

期刊

DIGESTIVE AND LIVER DISEASE
卷 54, 期 2, 页码 207-213

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.dld.2021.07.008

关键词

Anti-TNF failure; Clinical efficacy; Crohn's disease; Drug sustainability; Ustekinumab

资金

  1. National Research, Development and Innovation Office [FK 132834]
  2. New National Excellence Program of the Ministry of Human Capacities, Hungary [UNKP-21-4-II]

向作者/读者索取更多资源

The clinical efficacy, drug sustainability, dose intensification, and therapeutic drug monitoring of ustekinumab therapy in patients with Crohn's disease were evaluated in this prospective, nationwide, multicenter cohort study. The study found that ustekinumab showed favorable drug sustainability and clinical efficacy in patients with severe disease phenotype and previous anti-tumor necrosis factor failure. However, frequent dose intensification was required.
Introduction: Although efficacy of ustekinumab (UST) has been demonstrated through randomized trials, data from real-life prospective cohorts are still limited. Our aim was to evaluate clinical efficacy, drug sustainability, dose intensification and results from therapeutic drug monitoring in UST treated patients with Crohn's disease (CD) using a prospective, nationwide, multicenter cohort. Methods: Patients from 10 Inflammatory Bowel Disease centers were enrolled between 2019 January and 2020 May. Patient demographics, disease phenotype, treatment history, clinical disease activity (Crohn's Disease Activity Index(CDAI), Harvey Bradshaw Index(HBI)), biomarkers, and serum drug levels were obtained. Evaluations were performed at week8 (post-induction), w16-20, w32-36, and w52-56 follow-up visits. Results: A total of 142 patients were included [57.4% female; complex disease behavior (B2/B3):48%, previous anti-TNF exposition:97%]. Clinical response and remission rates after induction(w8) were 78.1% and 57.7% using CDAI, and 82.5% and 51.8% based on HBI scores. The one-year clinical remission rate was 58%/57.3%(CDAI/HBI). Composite clinical and biomarker remission (CDAI < 150 and C-reactive protein < 10 mg/L) rates were 35.4%; 33.3%; 38.6% and 36.6% at w8/w16-20/w32-36 and w52-56. Drug sustainability was 81.9%(standard deviation(SD): 3.4) at 1 year(1y). Probability of dose intensification was high and introduced early, 42.2%(SD:4.2) at similar to w32 and 51.9%(SD:4.4%) at 1y. Conclusion: Ustekinumab showed favorable drug sustainability and clinical efficacy in a patient population with severe disease phenotype and previous anti-tumor necrosis factor (anti-TNF) failure, however frequent dose intensification was required. (C) 2021 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

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