Early Ultrasound Response and Progressive Transmural Remission After Treatment With Ustekinumab in Crohn’s Disease

医学 乌斯特基努马 克罗恩病 内科学 钙蛋白酶 胃肠病学 临床终点 炎症性肠病 随机对照试验 多中心试验 疾病 多中心研究 英夫利昔单抗
作者
Torsten Kucharzik,Rune Wilkens,Maria Antonietta D’Agostino,Giovanni Maconi,Manuela Le Bars,Marjolein Lahaye,Ivana Bravatà,Maciej Nazar,Lioudmila Ni,E. Ercole,Mariangela Allocca,Naděžda Machková,Floris A.E. de Voogd,Carolina Palmela,Rose Vaughan,Christian Maaser,Tomáš Grega,I. Niangová,Rudolf Repák,Petra Matějková,Radka Vaníčková,Juel Mie Agerbæk,Annett G. Cannon,Vittorio Giuliano,Christoph Antoni,Jürgen Büning,M Gebel,Martin Grewe,Sebastian Küpper,Nikolas Ryschka,Andrej Potthoff,Wolfgang Reindl,Karolin Schliwa,Martin Schulz,H Schulze,Markus Krankenhaus,Marco Affronti,Laura Menicagli,Cristina Bezzio,Flaminia Cavallaro,Marina Coletta,Andrea Costantino,Federica Furfaro,Fabrizio Pizzolante,Steven Bots,Robert J. de Knegt,Ivan Bunganič,Zdenek Opravil,Joaquín Poza,Jordi Rimola,Cristina Suárez Ferrer
出处
期刊:Clinical Gastroenterology and Hepatology [Elsevier BV]
卷期号:21 (1): 153-163.e12 被引量:35
标识
DOI:10.1016/j.cgh.2022.05.055
摘要

In this STARDUST substudy, the effect of ustekinumab on transmural bowel inflammation was assessed in adults with moderate-to-severe Crohn's disease (CD) by using intestinal ultrasound (IUS), a noninvasive imaging procedure.STARDUST was an international, multicenter, phase 3b, interventional, randomized controlled trial specifically designed to compare treat-to-target and standard-of-care treatment strategies in ustekinumab-treated CD patients. In this substudy, the most affected bowel segment at baseline by IUS was used for all analyses. Key IUS endpoints (centrally read, parameter-blinded) were IUS response, transmural remission, bowel wall thickness (BWT), blood flow, bowel wall stratification, and inflammatory fat.Seventy-seven patients were evaluated. IUS response could be determined 4 weeks after treatment initiation, with progressive improvement through week 48. IUS response and transmural remission rates at week 48 were 46.3% and 24.1%, respectively. IUS response, transmural remission, BWT, and blood flow normalization rates were more pronounced in the colon and biologic-naive patients. Fair/moderate reliability (κ = 0.21-0.51) was observed between week 4 IUS response and week 48 overall endoscopic response and fecal calprotectin/complete biomarker outcomes. Endoscopy and IUS baseline agreement was >90% in determining the terminal ileum as the most affected bowel segment. IUS response absence at week 4 was associated with no endoscopic response (based on the simplified endoscopic score for Crohn's disease terminal ileum subscore) at week 48 (negative predictive value = 73%).In this first international, multicenter, interventional study, IUS showed that ustekinumab-treated CD patients achieved progressive IUS response (46.3%) and transmural remission (24.1%) through week 48, with a more robust response in the colon and biologic-naive patients.gov number: NCT03107793.

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