Cyclosporine microemulsion and tacrolimus are associated with decreased chronic allograft failure and improved long-term graft survival as compared with Sandimmune

被引:38
作者
Meier-Kriesche, HU [1 ]
Kaplan, B [1 ]
机构
[1] Univ Michigan, Hlth Syst, Dept Internal Med, Taubman Ctr 3914, Ann Arbor, MI 48109 USA
关键词
cyclosporine; graft survival; tacrolimus; transplantation;
D O I
10.1034/j.1600-6143.2002.020116.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Tacrolimus and cyclosporine in the microemulsion formulation Neoral(R) have demonstrated improvements in acute rejection rates after renal transplantation compared with conventional cyclosporine formulation, Sandimmune(R). To evaluate whether these drugs are also associated with improvements in chronic allograft failure (CAF) rates, we retrospectively analyzed 32 040 primary renal allograft recipients reported to the United States Renal Data System (USRDS) between 1994 and 1997. Graft loss secondary to CAF was defined as graft loss beyond 6 months post-transplant, censored for death, acute rejection, thrombosis, infections and noncompliance. A Cox proportional hazard model was used to investigate the relationship between graft loss secondary to CAF and the use of conventional cyclosporine formulation, as opposed to cyclosporine microemulsion and tacrolimus (Prograf(R)). The analysis was correcrted for confounding variables, such as acute rejection, sex, race, human leukocyte antigen (HLA) mismatch, % panel reactive antibodies (PRA), delayed graft function (DGF), cold ischemia time, induction therapy, dialysis time, etiology of end-stage renal disease, cytomegalovirus (CMV) risk group, donor source, era effect, and mycophenolate mofetil (MMF) use. Cyclosporine microemulsion use was associated with a significantly lower relative risk (RR = 0.6, Cl = 0.5-0.7) for CAF as opposed to conventional cyclosporine formulation. Likewise tacrolimus as compared with conventional cyclosporine formulation was associated with a significantly lower relative risk (RR = 0.7, Cl = 0.6-0.8) for CAP Conventional cyclosporine formulation treatment was associated with a 87.6% adjusted CAF-free survival rate at 4 years. Both tacrolimus and cyclosporine microemulsion were associated with a significantly better adjusted CAF-free survival at 4 years (91.4 and 92.4%, respectively). Both cyclosporine microemulsion and tacrolimus are associated with improved graft survival and a decreased relative risk for CAF when compared with the older conventional cyclosporine formulation. This association is independent of the use of MMF or changes in era.
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页码:100 / 104
页数:5
相关论文
共 16 条
[1]  
FOLLARD SG, 1999, TRANSPLANTATION, V68, P1325
[2]   FK506 IN SOLID-ORGAN TRANSPLANTATION [J].
FUNG, JJ ;
STARZL, TE .
THERAPEUTIC DRUG MONITORING, 1995, 17 (06) :592-595
[3]  
Haustein UF, 1998, J EUR ACAD DERMATOL, V11, P1
[4]   Tacrolimus (FK 506) in kidney transplantation: Three-year survival results of the US multicenter, randomized, comparative trial [J].
Jensik, SC .
TRANSPLANTATION PROCEEDINGS, 1998, 30 (04) :1216-1218
[5]  
Johnson C, 2000, TRANSPLANTATION, V69, P834
[6]  
KAHAN BD, 1995, TRANSPLANTATION, V59, P505
[7]  
Kahan BD, 2000, J AM SOC NEPHROL, V11, P1122, DOI 10.1681/ASN.V1161122
[8]  
KOVARIK JM, 1994, TRANSPLANTATION, V58, P658
[9]   REDUCED INTERINDIVIDUAL AND INTRAINDIVIDUAL VARIABILITY IN CYCLOSPORINE PHARMACOKINETICS FROM A MICROEMULSION FORMULATION [J].
KOVARIK, JM ;
MUELLER, EA ;
VANBREE, JB ;
TETZLOFF, W ;
KUTZ, K .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (03) :444-446
[10]   Multicenter randomized trial comparing tacrolimus (FK506) and cyclosporine in the prevention of renal allograft rejection - A report of the European Tacrolimus Multicenter Renal Study Group [J].
Mayer, AD ;
Dmitrewski, J ;
Squifflet, JP ;
Besse, T ;
Grabensee, B ;
Klein, B ;
Eigler, FW ;
Heemann, U ;
Pichlmayr, R ;
Behrend, M ;
Vanrenterghem, Y ;
Donck, J ;
vanHooff, J ;
Christiaans, M ;
Morales, JM ;
Andres, A ;
Johnson, RWG ;
Short, C ;
Buchholz, B ;
Rehmert, N ;
Land, W ;
Schleibner, S ;
Forsythe, JLR ;
Talbot, D ;
Neumayer, HH ;
Hauser, I ;
Ericzon, BG ;
Brattstrom, C ;
Claesson, K ;
Muhlbacher, F ;
Pohanka, E .
TRANSPLANTATION, 1997, 64 (03) :436-443