Conversion of Long-Term Kidney Transplant Recipients From Calcineurin Inhibitor Therapy to Everolimus: A Randomized, Multicenter, 24-Month Study

被引:125
作者
Holdaas, Hallvard [1 ]
Rostaing, Lionel [2 ]
Seron, Daniel [3 ]
Cole, Edward [4 ]
Chapman, Jeremy [5 ]
Fellstrom, Bengt [6 ]
Strom, Erik H. [7 ]
Jardine, Alan [8 ]
Midtvedt, Karsten [9 ]
Machein, Uwe [10 ]
Ulbricht, Bettina [10 ]
Karpov, Alexander [10 ]
O'Connell, Philip J. [5 ]
机构
[1] Univ Oslo, Rikshosp, Dept Med, N-0027 Oslo, Norway
[2] CHU Rangueil, Dept Nephrol Dialysis & Organ Transplantat, F-31054 Toulouse, France
[3] Univ Autonoma Barcelona, Dept Nephrol, Hosp Vall Hebron, Barcelona, Spain
[4] Univ Toronto, Toronto Gen Hosp, Div Nephrol, Toronto, ON M5G 1L7, Canada
[5] Univ Sydney, Westmead Hosp, Ctr Transplant & Renal Res, Westmead Millennium Inst, Sydney, NSW 2006, Australia
[6] Univ Uppsala Hosp, Dept Med Sci, Renal Unit, Uppsala, Sweden
[7] Oslo Univ Hosp, Dept Pathol, Oslo, Norway
[8] Univ Glasgow, Glasgow Cardiovasc Res Ctr, Fac Med, Glasgow, Lanark, Scotland
[9] Oslo Univ Hosp, Rikshosp, Dept Nephrol, Dept Med, Oslo, Norway
[10] Novartis Pharma AG, Basel, Switzerland
关键词
Enteric-coated mycophenolate sodium; Renal transplantation; Acute rejection; CHRONIC ALLOGRAFT NEPHROPATHY; GLOMERULAR-FILTRATION-RATE; LOW-GRADE PROTEINURIA; RENAL-TRANSPLANTATION; GRAFT-SURVIVAL; CYCLOSPORINE-A; MAINTENANCE IMMUNOSUPPRESSION; EXPOSURE CYCLOSPORINE; OPEN-LABEL; SIROLIMUS;
D O I
10.1097/TP.0b013e318224c12d
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Background. Benefits of conversion from calcineurin inhibitor (CNI) to mammalian target of rapamycin inhibitor-based immunosuppression in long-term kidney transplant patients remain uncertain. Methods. ASCERTAIN was a 24-month, open-label, multicenter study. Kidney transplant patients more than 6 months posttransplant receiving CNI (baseline glomerular filtration rate [GFR] 30-70 mL/min/1.73 m(2)) were randomized to everolimus with CNI elimination (n = 127) or CNI minimization (n = 144), or continued CNI unchanged (controls, n = 123) to assess the effect on measured GFR at month 24 after randomization. Results. Renal function was stable in all groups to month 24. Mean measured GFR at month 24, the primary endpoint, was 48.0 +/- 22.0 mL/min/1.73 m(2), 46.6 +/- 21.1 mL/min/1.73 m(2), and 46.0 +/- 20.4 mL/min/1.73 m(2) in the CNI elimination, CNI minimization, and control groups, respectively. Differences between CNI elimination (1.12 mL/min/1.73 m(2), 95% confidence interval [CI] -3.51 to 5.76, P=0.63) and CNI minimization (0.59 mL/min/1.73 m(2), 95% CI -3.88 to 5.07, P=0.79) versus controls at month 24 were nonsignificant that is, the primary endpoint was not met. No efficacy endpoint differed significantly between groups. Post hoc analyses showed that patients with baseline creatinine clearance (CrCl) more than 50 mL/min had a significantly greater increase in measured GFR after CNI elimination versus controls (difference 11.4 mL/min/1.73 m(2), 95% CI 2.1 to 20.8 mL/min/1.73 m(2), P=0.017). Adverse events resulted in discontinuation in 36 (28.3%) CNI elimination patients, 24 (16.7%) CNI minimization patients, and 5 (4.1%) controls (P<0.001 vs. CNI elimination; P=0.020 vs. CNI minimization). Conclusion. Conversion to everolimus with CNI elimination or minimization a mean of 5.6 years after kidney transplantation had no overall renal benefit and was associated with more frequent adverse events and discontinuations. Patients with CrCl more than 50 mL/min may benefit from a change in therapy more than 6 months after renal transplantation.
引用
收藏
页码:410 / 418
页数:9
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