Corticosteroid-free immunosuppression with tacrolimus, mycophenolate mofetil, and Daclizumab induction in renal transplantation

被引:197
作者
Rostaing, L
Cantarovich, D
Mourad, G
Budde, K
Rigotti, P
Mariat, C
Margreiter, R
Capdevilla, L
Lang, P
Vialtel, P
Ortuño-Mirete, J
Charpentier, B
Legendre, C
Sanchez-Plumed, J
Oppenheimer, F
Kessler, M
机构
[1] Rangueil Univ Hosp, Multiorgan Transplant Unit, F-31059 Toulouse, France
[2] CHU Nantes, Inst Transplantat & Rech Transplantat, F-44035 Nantes, France
[3] Hop Lapeyronie, Serv Nephrol & Transplantat, Montpellier, France
[4] Univ Klin, Charite, Berlin, Germany
[5] Univ Hosp, Dept Med & Surg Sci, Padua, Italy
[6] CHU St Etienne, Hop Nord, St Etienne, France
[7] Landeskrankenhaus Innsbruck, Innsbruck, Austria
[8] Hosp Gen Valle Hebron, Unidad Dialisis, Barcelona, Spain
[9] Hop Henri Mondor, Serv Nephrol, F-94010 Creteil, France
[10] CHU Nord, Hop Michallon, Grenoble, France
[11] Hosp La Paz, Serv Nefrol, E-28046 Madrid, Spain
[12] Hop Bicetre, Serv Nephrol, Le Kremlin Bicetre, France
[13] Hop St Louis, Serv Nephrol, Paris, France
[14] Univ Valencia, Hosp La Fe, Serv Nefrol, Valencia, Spain
[15] Hosp Clin Barcelona, Serv Nefrol, Barcelona, Spain
[16] Hop Brabois Adulte, Les Nancy, France
关键词
tacrolimus; Daclizumab; mycophenolate mofetil; corticosteroid-free; renal transplantation;
D O I
10.1097/01.TP.0000154915.20524.0A
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Corticosteroid-free maintenance immunosuppression after organ transplantation eliminates the well-known corticosteroid-related side effects and may help to improve long-term outcome. We investigated whether a corticosteroid-free tacrolimus (Tac)/mycophenolate mofetil (MMF) regimen, in combination with daclizumab (Dac) induction therapy, provides adequate immunosuppression after renal transplantation. Methods. This 6-month, open-label, multicenter, parallel-group study involved 538 renal patients randomized (1:1) to a Dac/Tac/MMF regimen (n = 260) or a Tac/MMF/corticosteroids regimen (n = 278) as a control group. Results. Of the patients who completed the study, 88.8% in the Dac/Tac/MMF group were free from corticosteroid therapy at month 6. The incidence of biopsy-proven acute rejection was 16.5% in both treatment groups; the incidence of biopsyproven corticosteroid-resistant acute rejection was 4.3% and 5.0% with Tac/MMF/corticosteroids and Dac/Tac/MMF, respectively (P = NS for both comparisons). Renal function was also similar in both groups: median serum creatinine at month 6 was 125.0 mu mol/L (Tac/MMF/corticosteroids) and 131.0 mu ml/L (Dac/Tac/MMF), P = 0.277. The overall safety profile was similar with both regimens. However, compared with the Tac/MMF/steroid regimen, a significantly reduced incidence of new-onset insulin-dependent diabetes mellitus (5.4% vs. 0.4%, P = 0.003) was found with steroid-free immunosuppression. Moreover, mean total cholesterol concentrations increased from baseline in the Tac/MMF/corticosteroids group by 0.19 mmol/L, whereas in the Dac/Tac/MMF group, levels decreased by 0.19 mmol/L, P = 0.005. Conclusions. Corticosteroid-free immunosuppression with a Dac/Tac/MMF regimen is as effective at preventing acute rejection after renal transplantation as a standard triple regimen of Tac/MMF/corticosteroids. Furthermore, the safety benefits reported with Dac/Tac/MMF treatment may help improve the long-term outcome for renal-transplant patients.
引用
收藏
页码:807 / 814
页数:8
相关论文
共 21 条
[1]   Dadizumab - A review of its use in the management of organ transplantation [J].
Carswell, CI ;
Plosker, GL ;
Wagstaff, AJ .
BIODRUGS, 2001, 15 (11) :745-773
[2]   Issues of adherence to immunosuppressant therapy after solid-organ transplantation [J].
Chisholm, MA .
DRUGS, 2002, 62 (04) :567-575
[3]   Steroid withdrawal from tacrolimus-based therapy in renal transplant patients [J].
Citterio, F ;
Rigotti, P ;
Scatà, MC ;
Romagnoli, J ;
Baldan, N ;
Marchini, F ;
Castagneto, M .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (05) :1707-1708
[4]   Risk factors for and management of post-transplantation cardiovascular disease [J].
Fellström, B .
BIODRUGS, 2001, 15 (04) :261-278
[5]  
Kasiske BL, 2000, J AM SOC NEPHROL, V11, P1735, DOI 10.1681/ASN.V1191735
[6]   The use of an anti-CD25 monoclonal antibody and mycophenolate mofetil enables the use of a low-dose tacrolimus and early withdrawal of steroids in renal transplant recipients [J].
Kuypers, DRJ ;
Evenepoel, P ;
Maes, B ;
Coosemans, W ;
Pirenne, J ;
Vanrenterghem, Y .
CLINICAL TRANSPLANTATION, 2003, 17 (03) :234-241
[7]   GLUCOCORTICOID-INDUCED OSTEOPOROSIS - PATHOGENESIS AND MANAGEMENT [J].
LUKERT, BP ;
RAISZ, LG .
ANNALS OF INTERNAL MEDICINE, 1990, 112 (05) :352-364
[8]   Five preventable causes of kidney graft loss in the 1990s: A single-center analysis [J].
Matas, AJ ;
Humar, A ;
Gillingham, KJ ;
Payne, WD ;
Gruessner, RWG ;
Kandaswamy, R ;
Dunn, DL ;
Najarian, JS ;
Sutherland, DER .
KIDNEY INTERNATIONAL, 2002, 62 (02) :704-714
[9]   Efficacy and safety of tacrolimus compared with cyclosporine microemulsion in kidney transplantation:: Twelve-month follow-up [J].
Montagnino, G ;
Krämer, BK ;
Arias, M .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (05) :1635-1637
[10]   Long-term survival in renal transplant recipients with graft function [J].
Ojo, AO ;
Hanson, JA ;
Wolfe, RA ;
Leichtman, AB ;
Agodoa, LY ;
Port, FK .
KIDNEY INTERNATIONAL, 2000, 57 (01) :307-313