Infliximab Exposure Associates With Radiologic Evidence of Healing in Patients With Crohn's Disease.


Journal

Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
ISSN: 1542-7714
Titre abrégé: Clin Gastroenterol Hepatol
Pays: United States
ID NLM: 101160775

Informations de publication

Date de publication:
05 2021
Historique:
received: 16 01 2020
revised: 06 04 2020
accepted: 17 04 2020
pubmed: 4 5 2020
medline: 19 8 2021
entrez: 4 5 2020
Statut: ppublish

Résumé

Higher infliximab trough levels are associated with clinical and endoscopic remission in patients with Crohn's disease (CD). We investigated pharmacodynamic features of infliximab and radiological healing. We performed a substudy of the TAILORIX trial (patients with active luminal CD in Europe, treated with infliximab), analyzing baseline and week 54 magnetic resonance enterography (MRE) data. MREs were scored using the MaRIA score by blinded central readers. Radiologic response and remission were defined, based on MaRIA criteria in all segments, as scores below 11 and 7, respectively. We collected data on infliximab trough levels, biomarkers, and endoscopic findings. Our primary aim was to evaluate pharmacodynamic features associated with radiologic response and remission, based on MRE assessments at baseline and at 54 weeks after initiation of infliximab therapy. We analyzed data from 36 patients (50% female; median age 35.7 years; interquartile age range, 25.6-48.6 years; median disease duration, 1.5 months; interquartile duration range, 0.6-22.4 months). At week 54 of treatment, 36.4% of patients had a radiologic response, 30.3% of patients were in remission, and 71% had endoscopic features of remission. At baseline, there was a correlation between the CD endoscopic index of severity and MaRIA scores (κ = 0.46; P = .008), but we found no correlation at week 54 (κ = 0.06; P = .75). Radiologic remission correlated with infliximab trough level at week 14 (P = .049) when the infliximab trough level cut-off value was set at 7.8 μg/mL (area under the curve, 0.74; 75% sensitivity; 86% specificity; 90% negative predictive value; 57% positive predictive value). Radiologic response correlated with infliximab trough levels at week 14 (P = .048) when the infliximab trough level cut-off value was set at 7.8 μg/mL (area under the curve, 0.73; 70% sensitivity; 90% specificity; 86% negative predictive value; 78% positive predictive value) and with continuous pharmacologic evidence of response (infliximab trough levels above 5.0 μg/mL at all time points) (P = .034). In a substudy of data from the TAILORIX trial of patients with active luminal CD, we identified a relationship between exposure to infliximab and radiologic evidence of outcomes.

Sections du résumé

BACKGROUND & AIMS
Higher infliximab trough levels are associated with clinical and endoscopic remission in patients with Crohn's disease (CD). We investigated pharmacodynamic features of infliximab and radiological healing.
METHODS
We performed a substudy of the TAILORIX trial (patients with active luminal CD in Europe, treated with infliximab), analyzing baseline and week 54 magnetic resonance enterography (MRE) data. MREs were scored using the MaRIA score by blinded central readers. Radiologic response and remission were defined, based on MaRIA criteria in all segments, as scores below 11 and 7, respectively. We collected data on infliximab trough levels, biomarkers, and endoscopic findings. Our primary aim was to evaluate pharmacodynamic features associated with radiologic response and remission, based on MRE assessments at baseline and at 54 weeks after initiation of infliximab therapy.
RESULTS
We analyzed data from 36 patients (50% female; median age 35.7 years; interquartile age range, 25.6-48.6 years; median disease duration, 1.5 months; interquartile duration range, 0.6-22.4 months). At week 54 of treatment, 36.4% of patients had a radiologic response, 30.3% of patients were in remission, and 71% had endoscopic features of remission. At baseline, there was a correlation between the CD endoscopic index of severity and MaRIA scores (κ = 0.46; P = .008), but we found no correlation at week 54 (κ = 0.06; P = .75). Radiologic remission correlated with infliximab trough level at week 14 (P = .049) when the infliximab trough level cut-off value was set at 7.8 μg/mL (area under the curve, 0.74; 75% sensitivity; 86% specificity; 90% negative predictive value; 57% positive predictive value). Radiologic response correlated with infliximab trough levels at week 14 (P = .048) when the infliximab trough level cut-off value was set at 7.8 μg/mL (area under the curve, 0.73; 70% sensitivity; 90% specificity; 86% negative predictive value; 78% positive predictive value) and with continuous pharmacologic evidence of response (infliximab trough levels above 5.0 μg/mL at all time points) (P = .034).
CONCLUSIONS
In a substudy of data from the TAILORIX trial of patients with active luminal CD, we identified a relationship between exposure to infliximab and radiologic evidence of outcomes.

Identifiants

pubmed: 32360982
pii: S1542-3565(20)30597-8
doi: 10.1016/j.cgh.2020.04.052
pii:
doi:

Substances chimiques

Gastrointestinal Agents 0
Infliximab B72HH48FLU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

947-954.e2

Investigateurs

Guy Lambrecht (G)
Anthony Buisson (A)
Yoram Bouhnik (Y)
Janneke Vander Woude (JV)
Philippe Van Hootegem (P)
Jacques Moreau (J)
Edouard Louis (E)
Denis Franchimont (D)
Martine De Vos (M)
Fazia Mana (F)
Hedia Brixi (H)
Matthieu Allez (M)
Philip Caenepeel (P)
Alexandre Aubourg (A)
Bas Oldenburg (B)
Marieke Pierik (M)
Sylvie Chevret (S)

Informations de copyright

Copyright © 2021 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

Peter Bossuyt (P)

Department of Gastroenterology, Imelda GI Clinical Research Center, Imelda General Hospital, Bonheiden, Belgium; Department of Gastroenterology and Hepatology, University Hospitals Leuven, Catholic University of Leuven, Leuven, Belgium. Electronic address: peter.bossuyt@imelda.be.

Erwin Dreesen (E)

Department of Pharmaceutical and Pharmacological Sciences, Catholic University of Leuven, Leuven, Belgium.

Jordi Rimola (J)

IBD Unit, Radiology Department, Hospital Clínic of Barcelona, Barcelona, Spain.

Sofie Devuysere (S)

Department of Radiology, Imelda General Hospital, Bonheiden, Belgium.

Yves De Bruecker (Y)

Department of Radiology, Imelda General Hospital, Bonheiden, Belgium.

Ragna Vanslembrouck (R)

Department of Radiology, University Hospitals Leuven, Catholic University of Leuven, Leuven, Belgium.

Valérie Laurent (V)

INSERM U947 and Department of Radiology, Nancy University Hospital, Vandoeuvre-lès-Nancy, France.

Magaly Zappa (M)

Department of Radiology, Beaujon Hospital, Clichy, France.

Céline Savoye-Collet (C)

Department of Radiology, Rouen University Hospital, Normandy University, UNIROUEN, Rouen, France.

Benjamin Pariente (B)

Department of Gastroenterology, Hospital Claude Huriez, Lille, France.

Jérôme Filippi (J)

Department of Gastroenterology, Hospital Archet, Nice, France.

Filip Baert (F)

Department of Gastroenterology, AZ Delta, Roeselare, Belgium.

Geert D'Haens (G)

Department of Gastroenterology, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, the Netherlands.

David Laharie (D)

Department of Gastroenterology, Hôpital Haut-Lévêque, Bordeaux University Hospital, Pessac, France.

Laurent Peyrin-Biroulet (L)

INSERM U1256 NGERE and Department of Hepato-Gastroenterology, Nancy University Hospital, Vandoeuvre-lès-Nancy, France.

Séverine Vermeire (S)

Department of Gastroenterology and Hepatology, University Hospitals Leuven, Catholic University of Leuven, Leuven, Belgium.

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