Comparison of four different immunosuppression protocols without long-term steroid therapy in kidney recipients monitored by surveillance biopsy: Five-year outcomes

被引:68
作者
Kumar, Mysore S. Anil [1 ,2 ,3 ]
Saeed, M. Irfan [1 ,2 ,3 ]
Ranganna, Karthik [3 ,4 ,5 ]
Malat, Gregory [1 ,2 ,3 ]
Sustento-Reodica, Nedjema [3 ,6 ]
Kumar, Arjun M. S. [1 ,2 ,3 ]
Meyers, William C. [1 ,2 ,3 ]
机构
[1] Drexel Univ, Coll Med, Dept Surg, Philadelphia, PA 19102 USA
[2] Drexel Univ, Coll Med, Div Transplantat, Philadelphia, PA 19102 USA
[3] Med Coll Penn & Hahnemann Univ, Philadelphia, PA 19102 USA
[4] Drexel Univ, Coll Med, Dept Med, Philadelphia, PA 19102 USA
[5] Drexel Univ, Coll Med, Div Nephrol, Philadelphia, PA 19102 USA
[6] Drexel Univ, Coll Med, Dept Pathol, Philadelphia, PA 19102 USA
关键词
Immunosuppression protocol; Kidney transplant; Steroid withdrawal;
D O I
10.1016/j.trim.2008.08.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Induction and maintenance immunosuppression protocols with or without long-term steroid therapy in kidney transplant recipients are variable and are transplant center-specific. The aim of this prospective randomized pilot study was to compare 5-year outcomes in kidney recipients maintained on 4 different calcineurin inhibitor (CNI)-based immunosuppression protocols without long-term steroid therapy. Two hundred consenting patients who received kidney transplants between June 2000 and October 2004 were enrolled in 4 immunosuppression protocol groups, with 50 patients in each group: cyclosporine (CSA)/mycophenolate mofetil (MMF), CSA/sirolimus (SRL), tacrolimus (TAC)/MMF, and TAC/SRL Induction therapy was done with basiliximab and methylprednisolone. Steroids were withdrawn on post-transplant day 2, and long-term steroid therapy was not used. Demographic characteristics among the four groups were comparable: approximately 50% of the recipients were African American and >= 80% of the kidneys transplanted were from deceased donors. Clinical acute rejection (CAR) was confirmed by biopsy and treated with intravenous pulse steroid therapy. Steroid-unresponsive CAR was treated with Thymoglobulin. Surveillance biopsies were performed at 1, 6.12, 24, 36, 48, and 60 months to evaluate subclinical acute rejection (SCAR), chronic allograft injury (CAI), and other pathological changes per the Banff 2005 schema. The primary end point was CAR, and secondary end points were 5-year patient and graft survival rates, renal function, SCAR, CAI, and adverse events. In the first year post-transplant the incidence of CAR was 18% in the CSA/MMF group, 8% in the CSA/SRL group, 14% in the TAC/MMF group, and 14% in the TAC/SRL group (CSA/MMF vs. TAC/SRL; p = 0.05). The incidence of SCAR was 22% in the CSA/MMF group, 8% in the CSA/SRL group, 16% in the TAC/MMF group, and 6% in the TAC/SRL group (CSA/MMF vs. CSA/SRL and TAC/SRL; p = 0.05). After the first year, the incidences of CAR and SCAR decreased and were comparable in all 4 groups. At 5 years post-transplant. cumulative CAI due to interstitial fibrosis/tubular atrophy (IF/TA), hypertension (HTN), and chronic calcineurin inhibitor (CNI) toxicity was observed in 54%,48%, and 8% of the CSA/MMF group vs. 1656, 36%, and 12% of the CSA/SRL group vs. 38%,24% and 6% of the TAC/MMF group vs. 14%,25% and 12% of the TAC/SLR group (IF/TA: CSA/MMF vs. CSA/SRL and TAC/SRL; p = 0.04, HTN: CSA/MMF vs. TAC/MMF and TAC/SRL; p = 0.05, CNI toxicity: TAC/SRL and CSA/SRL vs. TAC/MMF; p = 0.05). Five-year patient and graft survival rates were 82% and 60% in the CSA/MMF group, 82% and 60% in the CSA/SRL group, 84% and 62% in the TAC/MMF group, and 82% and 64% in the TAC/SRL group (p = 0.9). Serum creatinine levels and creatinine clearances at 5 years were comparable among the groups. Our data show that the rates of CAR and SCAR in the first year post-transplant were significantly lower in the CSA/SRL and TAC/SRL groups and that cumulative CAI rates due to IF/TA and HTN at 5 years were significantly lower in the TAC/MMF, TAC/SRL, and CSA/SRL groups than in the CSA/MMF group. Despite significant differences in the incidences of CAR and SCAR and prevalence of different types of CAI at 5 years, renal function and patient and graft survival rates at 5 years were comparable among kidney recipients maintained on 4 different immunosuppression protocols without long-term steroid therapy. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 42
页数:11
相关论文
共 38 条
[1]  
American Diabetes Association, 2004, DIABETES CARE S1, V27, pS11, DOI DOI 10.2337/DIACARE.27.2007.S11
[2]   Switch from calcineurin inhibitors to sirolimus-induced renal recovery in heart transplant recipients in the midterm follow-up [J].
Bestetti, R ;
Theodoropoulos, TAD ;
Burdmann, EA ;
Abbud, M ;
Cordeiro, JA ;
Villafanha, D .
TRANSPLANTATION, 2006, 81 (05) :692-696
[3]   A randomized, double-blinded comparison of thymoglobulin versus Atgam for induction immunosuppressive therapy in adult renal transplant recipients [J].
Brennan, DC ;
Flavin, K ;
Lowell, JA ;
Howard, TK ;
Shenoy, S ;
Burgess, S ;
Dolan, S ;
Kano, JM ;
Mahon, M ;
Schnitzler, MA ;
Woodward, R ;
Irish, W ;
Singer, GG .
TRANSPLANTATION, 1999, 67 (07) :1011-1018
[4]   CYCLOSPORIN-A IN CADAVERIC ORGAN-TRANSPLANTATION [J].
CALNE, RY ;
WHITE, DJG ;
EVANS, DB ;
THIRU, S ;
HENDERSON, RG ;
HAMILTON, DV ;
ROLLES, K ;
MCMASTER, P ;
DUFFY, TJ ;
MACDOUGALL, BRD ;
WILLIAMS, R .
BRITISH MEDICAL JOURNAL, 1981, 282 (6268) :934-936
[5]   A Randomized long-term trial of tacrolimus/sirolimus versus tacrolimums/mycophenolate versus cyclosporine/sirolimus in renal transplantation: Three-year analysis [J].
Ciancio, G ;
Burke, GW ;
Gaynor, JJ ;
Ruiz, P ;
Roth, D ;
Kupin, W ;
Rosen, A ;
Miller, J .
TRANSPLANTATION, 2006, 81 (06) :845-852
[6]   Kidney allograft fibrosis and atrophy early after living donor transplantation [J].
Cosio, FG ;
Grande, JP ;
Larson, TS ;
Gloor, JM ;
Velosa, JA ;
Textor, SC ;
Griffin, MD ;
Stegall, MD .
AMERICAN JOURNAL OF TRANSPLANTATION, 2005, 5 (05) :1130-1136
[7]   EARLY FUNCTION AS THE PRINCIPAL CORRELATE OF GRAFT-SURVIVAL - A MULTIVARIATE-ANALYSIS OF 200 CADAVERIC RENAL-TRANSPLANTS TREATED WITH A PROTOCOL INCORPORATING ANTILYMPHOCYTE GLOBULIN AND CYCLOSPORINE [J].
HALLORAN, PF ;
APRILE, MA ;
FAREWELL, V ;
LUDWIN, D ;
SMITH, EK ;
TSAI, SY ;
BEAR, RA ;
COLE, EH ;
FENTON, SS ;
CATTRAN, DC .
TRANSPLANTATION, 1988, 46 (02) :223-228
[8]   Pim and Akt oncogenes are independent regulators of hematopoietic cell growth and survival [J].
Hammerman, PS ;
Fox, CJ ;
Birnbaum, MJ ;
Thompson, CB .
BLOOD, 2005, 105 (11) :4477-4483
[9]   Cyclosporine induces cancer progression by a cell-autonomous mechanism [J].
Hojo, M ;
Morimoto, T ;
Maluccio, M ;
Asano, T ;
Morimoto, K ;
Lagman, M ;
Shimbo, T ;
Suthanthiran, M .
NATURE, 1999, 397 (6719) :530-534
[10]   Withdrawal of steroid therapy in African American kidney transplant recipients receiving sirolimus and tacrolimus [J].
Hricik, DE ;
Knauss, TC ;
Bodziak, KA ;
Weigel, K ;
Rodriguez, V ;
Seaman, D ;
Siegel, C ;
Valente, J ;
Ak, JAS .
TRANSPLANTATION, 2003, 76 (06) :938-942