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      Type of calcineurin inhibitor and long-term outcomes following liver transplantation in patients with primary biliary cholangitis – an ELTR study

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          Abstract

          Background & Aims

          Tacrolimus has been associated with recurrence of primary biliary cholangitis (PBC) after liver transplantation (LT), which in turn may reduce survival. This study aimed to assess the association between the type of calcineurin inhibitor used and long-term outcomes following LT in patients with PBC.

          Methods

          Survival analyses were used to assess the association between immunosuppressive drugs and graft or patient survival among adult patients with PBC in the European Liver Transplant Registry. Patients who received a donation after brain death graft between 1990 and 2021 with at least 1 year of event-free follow-up were included.

          Results

          In total, 3,175 patients with PBC were followed for a median duration of 11.4 years (IQR 5.9–17.9) after LT. Tacrolimus (Tac) was registered in 2,056 (64.8%) and cyclosporin in 819 (25.8%) patients. Following adjustment for recipient age, recipient sex, donor age, and year of LT, Tac was not associated with higher risk of graft loss (adjusted hazard ratio [aHR] 1.07, 95% CI 0.92-1.25, p = 0.402) or death (aHR 1.06, 95% CI 0.90-1.24, p = 0.473) over cyclosporin. In this model, maintenance mycophenolate mofetil (MMF) was associated with a lower risk of graft loss (aHR 0.72, 95% CI 0.60-0.87, p <0.001) or death (aHR 0.72, 95% CI 0.59-0.87, p <0.001), while these risks were higher with use of steroids (aHR 1.31, 95% CI 1.13-1.52, p <0.001, and aHR 1.34, 95% CI 1.15-1.56, p <0.001, respectively).

          Conclusions

          In this large LT registry, type of calcineurin inhibitor was not associated with long-term graft or recipient survival, providing reassurance regarding the use of Tac post LT in the population with PBC. Patients using MMF had a lower risk of graft loss and death, indicating that the threshold for combination treatment with Tac and MMF should be low.

          Impact and implications:

          This study investigated the association between immunosuppressive drugs and the long-term survival of patients with primary biliary cholangitis (PBC) following donation after brain death liver transplantation. While tacrolimus has previously been related to a higher risk of PBC recurrence, the type of calcineurin inhibitor was not related to graft or patient survival among patients transplanted for PBC in the European Liver Transplant Registry. Additionally, maintenance use of mycophenolate was linked to lower risks of graft loss and death, while these risks were higher with maintenance use of steroids. Our findings should provide reassurance for physicians regarding the continued use of Tac after liver transplantation in the population with PBC, and suggest potential benefit from combination therapy with mycophenolate.

          Graphical abstract

          Highlights:

          • Long-term risks of graft loss or death were similar between patients with PBC on tacrolimus or cyclosporin after LT.

          • This finding supports the continued use of tacrolimus in this population.

          • Maintenance use of mycophenolate was associated with lower risks of graft loss and death.

          • Maintenance use of steroids selected a group of patients with unfavourable long-term outcomes.

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          Most cited references49

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          EASL Clinical Practice Guidelines: The diagnosis and management of patients with primary biliary cholangitis

          Primary biliary cholangitis (PBC) is a chronic inflammatory autoimmune cholestatic liver disease, which when untreated will culminate in end-stage biliary cirrhosis. Diagnosis is usually based on the presence of serum liver tests indicative of a cholestatic hepatitis in association with circulating antimitochondrial antibodies. Patient presentation and course can be diverse and risk stratification is important to ensure all patients receive a personalised approach to their care. The goals of treatment and management are the prevention of end-stage liver disease, and the amelioration of associated symptoms. Pharmacologic approaches in practice, to reduce the impact of the progressive nature of disease, currently include licensed therapies (ursodeoxycholic acid and obeticholic acid) and off-label therapies (fibric acid derivatives, budesonide). These clinical practice guidelines summarise the evidence for the importance of a structured, life-long and individualised, approach to the care of patients with PBC, providing a framework to help clinicians diagnose and effectively manage patients.
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            Primary Biliary Cholangitis: 2018 Practice Guidance from the American Association for the Study of Liver Diseases

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              • Record: found
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              EASL Clinical Practice Guidelines: Liver transplantation.

              (2016)
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                Author and article information

                Contributors
                Journal
                JHEP Rep
                JHEP Rep
                JHEP Reports
                Elsevier
                2589-5559
                25 April 2024
                August 2024
                25 April 2024
                : 6
                : 8
                : 101100
                Affiliations
                [1 ]Department of Gastroenterology and Hepatology, Erasmus MC Transplant Institute, University Medical Center Rotterdam, The Netherlands
                [2 ]European Society for Organ Transplantation, Amsterdam, The Netherlands
                [3 ]European Liver Transplant Registry, Department of Hepatobiliary and Pancreatic Surgery and Liver Transplantation AP-HP Hôpital Paul Brousse, Université Paris-Saclay Villejuif, France
                [4 ]Department of Hepatology and Gastroenterology, Institute for Clinical and Experimental Medicine, Prague, Czech Republic
                [5 ]Department of Surgery, Division of HPB & Transplant Surgery, Erasmus MC Transplant Institute, University Medical Center Rotterdam, The Netherlands
                [6 ]Reference Center for Inflammatory Biliary Diseases and Autoimmune Hepatitis, European Reference Network on Hepatological Diseases (ERN Rare-Liver), Saint-Antoine Hospital, Assistance Publique - Hôpitaux de Paris; Inserm UMR_S938, Saint-Antoine Research Center, Sorbonne University, Paris, France
                [7 ]Department of HPB Surgery, Liver Unit, Queen Elizabeth Hospital, Birmingham, United Kingdom
                [8 ]Institute of Liver Studies, King’s College Hospital, London, United Kingdom
                [9 ]The Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom
                [10 ]Edinburgh Transplant Centre, Royal Infirmary of Edinburgh, Edinburg, United Kingdom
                [11 ]Division of Transplantation, CLINTEC, Karolinska Institutet, Stockholm, Sweden
                [12 ]Department of Hepatology and Liver Transplantation, Royal Free Hospital, London, United Kingdom
                [13 ]Liver Unit, Cambridge University Hospitals NHS Foundation Trust, Cambridge NIHR Biomedical Research Centre, Cambridge, United Kingdom
                Author notes
                [* ]Corresponding author. Address: Erasmus MC, University Medical Center Department of Gastroenterology and Hepatology, Doctor Molewaterplein 40, NA building, Floor 6, 3015 GD Rotterdam, The Netherlands; Tel.: +31107044215. a.vandermeer@ 123456erasmusmc.nl
                [†]

                Collaborator group from European Liver and Intestine Transplant Association (ELITA) listed at the end of the manuscript.

                Article
                S2589-5559(24)00104-6 101100
                10.1016/j.jhepr.2024.101100
                11263784
                39045337
                3e8379a9-116b-4632-b560-fabaaaf668cd
                © 2024 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 12 December 2023
                : 9 April 2024
                : 16 April 2024
                Categories
                Research Article

                calcineurin inhibitors,graft survival,liver transplantation,primary biliary cholangitis,survival

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