Randomized trial of tacrolimus plus mycophenolate mofetil or azathioprine versus cyclosporine oral solution (modified) plus mycophenolate mofetil after cadaveric kidney transplantation: Results at 2 years

被引:112
作者
Ahsan, N
Johnson, C
Gonwa, T
Halloran, P
Stegall, M
Hardy, M
Metzger, R
Shield, C
Rocher, L
Scandling, J
Sorensen, J
Mulloy, L
Light, J
Corwin, C
Danovitch, G
Wachs, M
VanVeldhuisen, P
Salm, K
Tolzman, D
Fitzsimmons, WE
机构
[1] Univ Med & Dent New Jersey, Div Nephrol & Transplantat, New Brunswick, NJ 08903 USA
[2] Milton S Hershey Med Ctr, Hershey, PA 17104 USA
[3] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[4] Baylor Univ, Med Ctr, Dallas, TX 75246 USA
[5] Univ Alberta, Edmonton, AB TRG 2R8, Canada
[6] Univ Colorado, Denver, CO 80262 USA
[7] Columbia Presbyterian, New York, NY 10032 USA
[8] Translife, Orlando, FL 32804 USA
[9] Via Christ Med Ctr, Wichita, KS 67214 USA
[10] William Beaumont Hosp, Royal Oak, MI 48073 USA
[11] Stanford Univ, Palo Alto, CA 94305 USA
[12] Latter Day St Hosp, Salt Lake City, UT 84103 USA
[13] Med Coll Georgia, Augusta, GA 30912 USA
[14] Washington Hosp, Ctr Med, Washington, DC 20010 USA
[15] Univ Iowa, Iowa City, IA 52242 USA
[16] Univ Calif Los Angeles, Los Angeles, CA 90024 USA
[17] EMMES Corp, Potomac, MA USA
[18] Fujisawa Healthcare Inc, Deerfield, IL 60015 USA
关键词
D O I
10.1097/00007890-200107270-00014
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. A previous report described the I-year results of a prospective, randomized trial designed to investigate the optimal combination of immunosuppressants in kidney transplantation. Recipients of first cadaveric kidney allografts were treated with tacrolimus+mycophenolate mofetil (MMF), cyclosporine oral solution (modified) (CsA)+MMF, or tacrolimus+azathioprine (AZA). Results at I year revealed that optimal efficacy and safety were achieved with a regimen containing tacrolimus+MMF. The present report describes results at 2 years. Methods. Two hundred twenty-three recipients of first cadaveric kidney allografts were randomized to receive tacrolimus+MMF, CsA+MMF, or tacrolimus+AZA. All regimens contained corticosteroids, and antibody induction was used only in patients who experienced delayed graft function. Patients were followed up for 2 years. Results. The results at 2 years corroborate and extend the findings of the previous report. Patients randomized to either treatment arm containing tacrolimus experienced improved kidney function. New-onset insulin dependence remained in four, three, and four patients in the tacrolimus+MMF, CsA+MMF, and tacrolimus+AZA treatment arms, respectively. Furthermore, patients with delayed graft function/acute tubular necrosis who were treated with tacrolimus+MMF experienced a 23% increase in allograft survival compared with patients receiving CsA+MMF (P=0.06). Patients randomized to tacrolimus+MMF received significantly lower doses of MMF compared with those administered CsA+MMF. Conclusions. All three immunosuppressive regimens provided excellent safety and efficacy. However, the best results overall were achieved with tacrolimus+MMF. The combination may provide particular benefit to kidney allograft recipients who develop delayed graft function/acute tubular necrosis. Renal function at 2 years was better in the tacrolimus treatment groups compared with the CsA group.
引用
收藏
页码:245 / 250
页数:6
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