Vedolizumab Therapy is Ineffective for Primary Sclerosing Cholangitis in Patients With Inflammatory Bowel Disease: A GETAID Multicentre Cohort Study.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
27 Sep 2019
Historique:
pubmed: 6 5 2019
medline: 25 2 2020
entrez: 7 5 2019
Statut: ppublish

Résumé

Whether vedolizumab may be effective as a treatment for primary sclerosing cholangitis [PSC] in patients with inflammatory bowel disease [IBD] remains controversial. We performed a retrospective observational study of consecutive patients with IBD and PSC, treated with vedolizumab for at least 30 weeks in 22 centres of GETAID from January 2015 to June 2016. The outcomes included a decrease in the serum alkaline phosphatase [ALP] concentration of at least 50% from baseline to Week 30 or 54, a change in any serum liver enzymes concentrations, and an assessment of the efficacy and safety of vedolizumab in IBD. Among 75 patients with active IBD and PSC treated with vedolizumab, 21 patients discontinued vedolizumab before Week 30 [due to lack of efficacy in 19 and malignancy in two patients]. In the remaining 54 patients, a decrease in the serum ALP concentration of at least 50% from baseline to Weeks 30 and 54 was observed in four [7%] and four [11%] patients, respectively. No significant change was observed in serum liver enzyme concentrations at week 30 or 54. After a median follow-up period of 19.4 [14.0-29.9] months, nine cases of digestive neoplasia [colorectal neoplasia in seven and cholangiocarcinoma in two] were reported. In patients with IBD and PSC, vedolizumab did not improve serum liver enzyme concentrations at week 30 or 54. Nine cases of digestive cancer occurred during the follow-up period, confirming the need for a tight surveillance programme in this population.

Sections du résumé

BACKGROUND BACKGROUND
Whether vedolizumab may be effective as a treatment for primary sclerosing cholangitis [PSC] in patients with inflammatory bowel disease [IBD] remains controversial.
METHODS METHODS
We performed a retrospective observational study of consecutive patients with IBD and PSC, treated with vedolizumab for at least 30 weeks in 22 centres of GETAID from January 2015 to June 2016. The outcomes included a decrease in the serum alkaline phosphatase [ALP] concentration of at least 50% from baseline to Week 30 or 54, a change in any serum liver enzymes concentrations, and an assessment of the efficacy and safety of vedolizumab in IBD.
RESULTS RESULTS
Among 75 patients with active IBD and PSC treated with vedolizumab, 21 patients discontinued vedolizumab before Week 30 [due to lack of efficacy in 19 and malignancy in two patients]. In the remaining 54 patients, a decrease in the serum ALP concentration of at least 50% from baseline to Weeks 30 and 54 was observed in four [7%] and four [11%] patients, respectively. No significant change was observed in serum liver enzyme concentrations at week 30 or 54. After a median follow-up period of 19.4 [14.0-29.9] months, nine cases of digestive neoplasia [colorectal neoplasia in seven and cholangiocarcinoma in two] were reported.
CONCLUSIONS CONCLUSIONS
In patients with IBD and PSC, vedolizumab did not improve serum liver enzyme concentrations at week 30 or 54. Nine cases of digestive cancer occurred during the follow-up period, confirming the need for a tight surveillance programme in this population.

Identifiants

pubmed: 31056693
pii: 5485858
doi: 10.1093/ecco-jcc/jjz088
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Gastrointestinal Agents 0
vedolizumab 9RV78Q2002

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1239-1247

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 European Crohn’s and Colitis Organisation (ECCO). Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Benedicte Caron (B)

Department of Gastroenterology, Hôpitaux Universitaires de Strasbourg [Hôpital de Hautepierre] and INSERM U1113 IRFAC, Université de Strasbourg [Faculté de Médecine], Strasbourg, France.

Laurent Peyrin-Biroulet (L)

INSERM U954 and Department of Gastroenterology, Université de Lorraine, Nancy, France.

Benjamin Pariente (B)

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

Yoram Bouhnik (Y)

Department of Gastroenterology, IBD and Nutrition Support, Beaujon Hospital, University Paris 7 Denis Diderot, Clichy, France.

Philippe Seksik (P)

Department of Gastroenterology, AP-HP, Hôpital Saint-Antoine, ERL 1057 INSERM/UMRS 7203, UPMC Université Paris 6, Paris, France.

Guillaume Bouguen (G)

Department of Gastroenterology, Pontchaillou Hospital and Rennes University, Rennes, France.

Ludovic Caillo (L)

Department of Gastroenterology, Nimes University Hospital, Nimes, France.

David Laharie (D)

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

Franck Carbonnel (F)

Department of Gastroenterology, Bicetre University Hospital, APHP, Université Paris Sud, le Kremlin Bicêtre, Paris, France.

Romain Altwegg (R)

Department of Gastroenterology, Hôpital Saint-Eloi, University Hospital of Montpellier, Montpellier, France.

Catherine Reenaers (C)

Department of Gastroenterology, Liege University Hospital, Liege, Belgium.

Melanie Serrero (M)

Hôpital Nord, Centre d'investigation clinique Marseille Nord, Université Méditerranée, Marseille, France.

Caroline Trang-Poisson (C)

Department of Gastroenterology, Institut des Maladies de l'appareil Digestif [IMAD], University Hospital of Nantes, Nantes University, Nantes, France.

Stephane Nancey (S)

Department of Gastroenterology, Hospices Civils de Lyon and University Claude Bernard Lyon 1, Pierre-Benite, France.

Jerome Filippi (J)

Department of Gastroenterology and Clinical Nutrition, Nice University Hospital, University of Nice Sophia-Antipolis, Nice, France.

Vered Abitbol (V)

Department of Gastroenterology, Cochin Hospital, University Paris 5 Descartes, Paris, France.

Guillaume Savoye (G)

Department of Gastroenterology, Rouen University and Hospital, Rouen, France.

Lucine Vuitton (L)

Department of Gastroenterology, Besançon University Hospital, Besançon, France.

Stephanie Viennot (S)

Department of Gastroenterology, Caen University Hospital, Caen, France.

Mathurin Fumery (M)

Department of Gastroenterology, Amiens University Hospital, Amiens, France.

Maud Reymond (M)

Department of Hepato-Gastroenterology, University Hospital Estaing of Clermont-Ferrand, Université d'Auvergne, Clermont-Ferrand, France.

Jean-Pierre Bronowicki (JP)

INSERM U954 and Department of Gastroenterology, Université de Lorraine, Nancy, France.

Jean-Marie Reimund (JM)

Department of Gastroenterology, Hôpitaux Universitaires de Strasbourg [Hôpital de Hautepierre] and INSERM U1113 IRFAC, Université de Strasbourg [Faculté de Médecine], Strasbourg, France.

Aurelien Amiot (A)

Department of Gastroenterology, Henri Mondor Hospital, APHP, EC2M3-EA7375, Paris Est-Créteil Val de Marne University, Creteil, France.

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