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Early Ultrasound Response and Progressive Transmural Remission After Treatment With Ustekinumab in Crohn's Disease
T. Kucharzik, R. Wilkens, MA. D'Agostino, G. Maconi, M. Le Bars, M. Lahaye, I. Bravatà, M. Nazar, L. Ni, E. Ercole, M. Allocca, N. Machková, FAE. de Voogd, C. Palmela, R. Vaughan, C. Maaser, STARDUST Intestinal Ultrasound study group
Jazyk angličtina Země Spojené státy americké
Typ dokumentu multicentrická studie, klinické zkoušky, fáze III, časopisecké články
- MeSH
- biologické přípravky * MeSH
- Crohnova nemoc * diagnostické zobrazování farmakoterapie MeSH
- dospělí MeSH
- indukce remise MeSH
- kolon MeSH
- lidé MeSH
- reprodukovatelnost výsledků MeSH
- ustekinumab terapeutické užití MeSH
- výsledek terapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- klinické zkoušky, fáze III MeSH
- multicentrická studie MeSH
BACKGROUND & AIMS: 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. METHODS: 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. RESULTS: 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%). CONCLUSIONS: 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. CLINICALTRIALS: gov number: NCT03107793.
Ambulanzzentrum Gastroenterologie am Klinikum Lüneburg Lüneburg Germany
Digestive Disease Center Bispebjerg Hospital Copenhagen Denmark
Division of Gastroenterology Surgical Department Hospital Beatriz Ângelo Loures Portugal
Gastro Unit Section of Medicine Hvidovre Hospital Copenhagen Denmark
Gastroenterology Unit Department of Biomedical and Clinical Sciences
Gastroenterology Unit Mauriziano Hospital Turin Italy
IRCCS Humanitas Research Hospital Rozzano Milan Italy
Janssen Cilag B 5 Breda The Netherlands
Janssen Cilag Polska Sp Z o o Warsaw Poland
Janssen Cilag Russia Moscow Russian Federation
Janssen Cilag S p A Milan Italy
Janssen Cilag SARL Issy les Moulineaux France
Klinik für Allgemeine Innere Medizin und Gastroenterologie Klinikum Lüneburg Lüneburg Germany
Luigi Sacco University Hospital University of Milan Milan Italy
Citace poskytuje Crossref.org
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- $a BACKGROUND & AIMS: 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. METHODS: 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. RESULTS: 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%). CONCLUSIONS: 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. CLINICALTRIALS: gov number: NCT03107793.
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