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Long-term impact of preventive UDCA therapy after transplantation for primary biliary cholangitis.

Authors :
Corpechot C
Chazouillères O
Belnou P
Montano-Loza AJ
Mason A
Ebadi M
Eurich D
Chopra S
Jacob D
Schramm C
Sterneck M
Bruns T
Reuken P
Rauchfuss F
Roccarina D
Thorburn D
Gerussi A
Trivedi P
Hirschfield G
McDowell P
Nevens F
Boillot O
Bosch A
Giostra E
Conti F
Poupon R
Parés A
Reig A
Donato MF
Malinverno F
Floreani A
Russo FP
Cazzagon N
Verhelst X
Goet J
Harms M
van Buuren H
Hansen B
Carrat F
Dumortier J
Source :
Journal of hepatology [J Hepatol] 2020 Sep; Vol. 73 (3), pp. 559-565. Date of Electronic Publication: 2020 Apr 07.
Publication Year :
2020

Abstract

Background & Aims: Recurrence of primary biliary cholangitis (PBC) after liver transplantation (LT) is frequent and can impair graft and patient survival. Ursodeoxycholic acid (UDCA) is the current standard therapy for PBC. We investigated the effect of preventive exposure to UDCA on the incidence and long-term consequences of PBC recurrence after LT.<br />Methods: We performed a retrospective cohort study in 780 patients transplanted for PBC, between 1983-2017 in 16 centers (9 countries), and followed-up for a median of 11 years. Among them, 190 received preventive UDCA (10-15 mg/kg/day). The primary outcome was histological evidence of PBC recurrence. The secondary outcomes were graft loss, liver-related death, and all-cause death. The association between preventive UDCA and outcomes was quantified using multivariable-adjusted Cox and restricted mean survival time (RMST) models.<br />Results: While recurrence of PBC significantly shortened graft and patient survival, preventive exposure to UDCA was associated with reduced risk of PBC recurrence (adjusted hazard ratio [aHR] 0.41; 95% CI 0.28-0.61; p <0.0001), graft loss (aHR 0.33; 95% CI 0.13-0.82; p <0.05), liver-related death (aHR 0.46; 95% CI 0.22-0.98; p <0.05), and all-cause death (aHR 0.69; 95% CI 0.49-0.96; p <0.05). On RMST analysis, preventive UDCA led to a survival gain of 2.26 years (95% CI 1.28-3.25) over a period of 20 years. Exposure to cyclosporine rather than tacrolimus had a complementary protective effect alongside preventive UDCA, reducing the cumulative incidence of PBC recurrence and all-cause death.<br />Conclusions: Preventive UDCA after LT for PBC is associated with a reduced risk of disease recurrence, graft loss, and death. A regimen combining cyclosporine and preventive UDCA is associated with the lowest risk of PBC recurrence and mortality.<br />Lay Summary: Recurrence of primary biliary cholangitis after liver transplantation is frequent and can impair graft and patient survival. We performed the largest international study of transplanted patients with primary biliary cholangitis to date. Preventive administration of ursodeoxycholic acid after liver transplantation was associated with reduced risk of disease recurrence, graft loss, liver-related and all-cause mortality. A regimen combining cyclosporine and preventive ursodeoxycholic acid was associated with the best outcomes.<br />Competing Interests: Conflict of interest Dr. Corpechot reports receiving grants from Arrow and Intercept France, consulting fees from Intercept France, Inventiva Pharma and Genkyotex, and fees for teaching from Intercept France and GlaxoSmithKline France; Dr. Chazouillères, receiving grant support from Aptalis, fees for teaching from Mayoly Spindler, consulting fees from Genfit, and fees for teaching and consulting fees from Intercept; Dr. Schramm, receiving lecture fees from Falk Pharma; Dr. Reuken, receiving lecture fees from CSL Behring, consulting fees from Boston Scientific, and travel expenses from Merz Pharmaceuticals; Dr. Rauchfuss, receiving lecture fees from Chiesi, Novartis, Roche and Astellas; Dr. Verhelst, receiving travel grants from Falk Pharma; Dr. Bruns, receiving lecture fees from AbbVie, Norgine, Intercept Pharmaceuticals, and Falk Pharma, and consulting fees from Intercept Pharmaceuticals; Dr. Cazzagon receiving consulting fees from Intercept Pharmaceuticals. No other potential conflict of interest relevant to this article was reported. Please refer to the accompanying ICMJE disclosure forms for further details.<br /> (Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.)

Details

Language :
English
ISSN :
1600-0641
Volume :
73
Issue :
3
Database :
MEDLINE
Journal :
Journal of hepatology
Publication Type :
Academic Journal
Accession number :
32275981
Full Text :
https://doi.org/10.1016/j.jhep.2020.03.043