Early conversion to a sirolimus-based, calcineurin-inhibitor-free immunosuppression in the SMART trial: observational results at 24 and 36 months after transplantation

Guba, Markus and Pratschke, Johann and Hugo, Christian and Kraemer, Bernhard K. and Pascher, Andreas and Pressmar, Katharina and Hakenberg, Oliver and Fischereder, Michael and Brockmann, Jens and Andrassy, Joachim and Banas, Bernhard and Jauch, Karl-Walter (2012) Early conversion to a sirolimus-based, calcineurin-inhibitor-free immunosuppression in the SMART trial: observational results at 24 and 36 months after transplantation. TRANSPLANT INTERNATIONAL, 25 (4). pp. 416-423. ISSN 0934-0874,

Full text not available from this repository. (Request a copy)

Abstract

Early conversion to a calcineurin-inhibitor (CNI)-free maintenance immunosuppression with sirolimus (SRL), mycophenolate mofetil (MMF) and steroids was associated with an improved 1-year renal function as compared with a cyclosporine (CsA)-based regimen (SMART core-study). This observational follow-up describes 132 patients followed up within the SMART study framework for 36 months. At 36 months, renal function continued to be superior in SRL-treated patients [ITT-eGFR@36m: 60.88 vs. 53.72 (CsA) ml/min/1.73 m2, P = 0.031]. However, significantly more patients discontinued therapy in the SRL group 59.4% vs.42.3% (CsA). Patient [99% (SRL) vs.97% (CsA) and graft 96% (SRL) vs.94% (CsA)] survival at 36 months was excellent in both arms. There was no difference in late rejection episodes. Late infections and adverse events were similar in both arms except of a higher rate of hyperlipidemia in SRL and a higher incidence of malignancy in CsA-treated patients. In a multivariate analysis, donor age >60 years, S-creatinine at conversion >2 mg/dl, CMV naive(-) recipients and immunosuppression with CsA were predictive of an impaired renal function at 36 months. Early conversion to a CNI-free SRL-based immunosuppression is associated with a sustained improvement of renal function up to 36 months after transplantation. Patient selection will be key to derive long-term benefit and avoid treatment failure using this mTOR-inhibitor-based immunosuppressive regimen.

Item Type: Article
Uncontrolled Keywords: RENAL-ALLOGRAFT RECIPIENTS; MYCOPHENOLATE-MOFETIL; CYTOMEGALOVIRUS-INFECTION; EFFICACY; SAFETY; RISK; MULTICENTER; EVEROLIMUS; EXPOSURE; THERAPY; calcineurin-inhibitor-free immunosuppression; kidney transplantation; mammalian target of rapamycin; sirolimus
Divisions: Medicine > Lehrstuhl für Innere Medizin II
Depositing User: Dr. Gernot Deinzer
Date Deposited: 15 May 2020 07:44
Last Modified: 15 May 2020 07:44
URI: https://pred.uni-regensburg.de/id/eprint/18991

Actions (login required)

View Item View Item