High-Dose Infliximab Rescue Therapy for Hospitalized Acute Severe Ulcerative Colitis Does Not Improve Colectomy-Free Survival.


Journal

Digestive diseases and sciences
ISSN: 1573-2568
Titre abrégé: Dig Dis Sci
Pays: United States
ID NLM: 7902782

Informations de publication

Date de publication:
02 2019
Historique:
received: 06 03 2018
accepted: 29 10 2018
pubmed: 18 11 2018
medline: 26 3 2019
entrez: 18 11 2018
Statut: ppublish

Résumé

Optimization strategies with infliximab (IFX) are increasingly used as rescue therapy for steroid refractory acute severe ulcerative colitis (ASUC). We aim to determine if intensified IFX induction improves colectomy rate and identifies outcome predictors. Hospitalized adult patients who received IFX for ASUC between 2010 and 2016 were identified. We compared standard inductions (5 mg/kg) vs high-dose induction (10 mg/kg) with 3-month colectomy rate as primary outcome. Seventy-two patients (62.5% male, median age 38.5) were identified. Thirty-seven patients (51.3%) received 5 mg/kg IFX and 35 received 10 mg/kg. Baseline clinical, biochemical and endoscopic parameters were well matched between these two groups. 10 mg/kg was more likely to be used by clinicians from 2014 onwards (p < 0.001). Three-month colectomy rate was 9.7%; which was not significantly different between the standard (5.4%) and high-dose (14.3%) IFX induction (p = 0.205). CRP ≥ 60 (OR 10.9 [95% CI 1.23-96.50], p = 0.032), hemoglobin ≤ 90 g/L (OR 15.6 [95% CI 2.61-92.66], p = 0.036) and albumin < 30 g/L (OR 9.4 [95% CI 1.06-83.13], p = 0.044) were associated with increased risk of colectomy at 3 months in univariate regression analysis. Use of high-dose infliximab rescue therapy did not improve 3-month colectomy-free survival in this cohort. Tailored use in high-risk patients may be beneficial although further validation is required.

Sections du résumé

BACKGROUND AND OBJECTIVE
Optimization strategies with infliximab (IFX) are increasingly used as rescue therapy for steroid refractory acute severe ulcerative colitis (ASUC). We aim to determine if intensified IFX induction improves colectomy rate and identifies outcome predictors.
METHODS
Hospitalized adult patients who received IFX for ASUC between 2010 and 2016 were identified. We compared standard inductions (5 mg/kg) vs high-dose induction (10 mg/kg) with 3-month colectomy rate as primary outcome.
RESULTS
Seventy-two patients (62.5% male, median age 38.5) were identified. Thirty-seven patients (51.3%) received 5 mg/kg IFX and 35 received 10 mg/kg. Baseline clinical, biochemical and endoscopic parameters were well matched between these two groups. 10 mg/kg was more likely to be used by clinicians from 2014 onwards (p < 0.001). Three-month colectomy rate was 9.7%; which was not significantly different between the standard (5.4%) and high-dose (14.3%) IFX induction (p = 0.205). CRP ≥ 60 (OR 10.9 [95% CI 1.23-96.50], p = 0.032), hemoglobin ≤ 90 g/L (OR 15.6 [95% CI 2.61-92.66], p = 0.036) and albumin < 30 g/L (OR 9.4 [95% CI 1.06-83.13], p = 0.044) were associated with increased risk of colectomy at 3 months in univariate regression analysis.
CONCLUSION
Use of high-dose infliximab rescue therapy did not improve 3-month colectomy-free survival in this cohort. Tailored use in high-risk patients may be beneficial although further validation is required.

Identifiants

pubmed: 30446928
doi: 10.1007/s10620-018-5358-z
pii: 10.1007/s10620-018-5358-z
doi:

Substances chimiques

Gastrointestinal Agents 0
Infliximab B72HH48FLU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

518-523

Commentaires et corrections

Type : CommentIn

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Auteurs

Che-Yung Chao (CY)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.
Department of Gastroenterology and Hepatology, Princess Alexandra Hospital, Brisbane, Australia.

Alex Al Khoury (A)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.

Achuthan Aruljothy (A)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.

Sophie Restellini (S)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.
Department of Gastroenterology and Hepatology, Geneva University Hospitals and University of Geneva, Geneva, Switzerland.

Jonathan Wyse (J)

Division of Gastroenterology, Jewish General Hospital, McGill University, Montreal, Canada.

Waqqas Afif (W)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.

Alain Bitton (A)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.

Peter L Lakatos (PL)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada.
Department of Gastroenterology, Semmelweis University, Budapest, Hungary.

Talat Bessissow (T)

Division of Gastroenterology, Montreal General Hospital, McGill University Health Centre, 1650 Avenue Cedar C7-200, Montreal, QC, H3G 1A4, Canada. talat.bessissow@mcgill.ca.

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