Conversion from a Calcineurin Inhibitor to Everolimus Therapy in Maintenance Liver Transplant Recipients: A Prospective, Randomized, Multicenter Trial

被引:135
作者
De Simone, Paolo [1 ]
Metselaar, Herold J. [2 ]
Fischer, Lutz [3 ]
Dumortier, Jerome [4 ]
Boudjema, Karim [5 ]
Hardwigsen, Jean [6 ]
Rostaing, Lionel [7 ]
De Carlis, Luciano [8 ]
Saliba, Faouzi [9 ]
Nevens, Frederik [10 ]
机构
[1] Azienda Osped Univ Pisana, Liver Transplantat Dept, I-56124 Pisa, Italy
[2] Erasmus MC, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[3] Univ Klinikum Hamburg Eppendorf, Chirurg Klin & Poliklin, Abt Hepatobiliare Chirurg, Hamburg, Germany
[4] Hop Edouard Herriot, Unite Transplantat Hepat, Lyon, France
[5] CHU Rennes, Hop Pontchaillou, Serv Chirurg Hepatobiliaire & Digest, Rennes, France
[6] Hop Conception, Dept Surg & Liver Transplantat, Marseille, France
[7] CHU Rangueil, Nephrol Dialysis & Multiorgan Transplant Unit, F-31054 Toulouse, France
[8] Osped Maggiore Niguarda, Dept Transplantat, Hepatobiliary Surg & Liver Transplantat Unit, Milan, Italy
[9] Univ Paris Sud, AP HP, Hop Paul Brousse, Ctr Hepatobiliaire, Villejuif, France
[10] Univ Ziekenhuis Gasthuisberg, Dept Hepatol, Louvain, Belgium
关键词
RENAL DYSFUNCTION; MYCOPHENOLATE-MOFETIL; SIROLIMUS CONVERSION; RISK-FACTORS; MONOTHERAPY; EFFICACY; SAFETY; IMMUNOSUPPRESSION; NEPHROTOXICITY; CYCLOSPORINE;
D O I
10.1002/lt.21827
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Calcineurin inhibitors (CNIs) contribute to renal dysfunction following liver transplantation. This prospective, randomized, multicenter, 6-month study (with an additional 6 months of follow-up) evaluated whether everolimus with CNI reduction or discontinuation would improve renal function in maintenance liver transplant recipients experiencing CNI-related renal impairment. Patients started everolimus therapy with CNI reduction or discontinuation (n = 72) or continued receiving standard-exposure CNI (n = 73). At month 6, 80% of the patients who had converted to everolimus had discontinued the CNI. The mean change in creatinine clearance (CrCl) from baseline to month 6 was similar between groups (everolimus, 1.0 +/- 10.2 mL/minute; controls, 2.3 +/- 7.8 mL/minute; P = 0.46), so the primary study endpoint (8 mL/minute difference in the change in CrCl) was not achieved. Among patients who continued everolimus according to the protocol, the mean increase in CrCl was 2.1 (n = 53) and 3.8 mL/minute (n = 38) at months 6 and 12, respectively, versus 2.4 (n = 68) and 3.5 mL/minute in controls (n = 51). The high frequency of CNI dose reductions in controls (77% of the patients) and the relatively long mean time post-transplant (>3 years) likely contributed to the small difference in CrCl. Biopsy-proven acute rejection occurred in 1.4% of the patients in each group, with no graft losses. Study drug discontinuation was higher in everolimus-treated patients, and adverse events were more frequent. These data demonstrate that everolimus allows for discontinuation or a major reduction of CNI exposure in liver allograft recipients suffering CNI-related renal dysfunction without a loss of efficacy. Trials targeting earlier conversion post-transplantation are required to confirm the efficacy and safety of everolimus for improving renal function after liver transplantation. Liver Transpl 15:1262-1269, 2009. (C) 2009 AASLD.
引用
收藏
页码:1262 / 1269
页数:8
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