RAD in de novo renal transplantation: Comparison of three doses on the incidence and severity of acute rejection

被引:79
作者
Kahan, BD
Kaplan, B
Lorber, MI
Winkler, M
Cambon, N
Boger, RS
机构
[1] Univ Texas, Sch Med, Div Immunol & Organ Transplantat, Houston, TX 77030 USA
[2] St Barnabas Hosp, Livingston, NJ USA
[3] Yale Univ, Sch Med, New Haven, CT USA
[4] Hannover Med Sch, Hannover, Germany
[5] Novartis Pharma AG, Basel, Switzerland
[6] Novartis Pharmaceut, E Hanover, NJ USA
关键词
D O I
10.1097/00007890-200105270-00008
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. The effects of three doses of RAD (40-O-[2-hydroxyethyl]-rapamycin), a novel macrolide with potent immunosuppressive and antiproliferative properties, on the incidence and severity of acute rejection episodes as well as its tolerability were evaluated in a dose-ranging study in de novo renal transplant recipients. Methods. In this double-blind, parallel group, multicenter study, recipients were randomized to receive 1 mg, 2 mg, or 4 mg/day of RAD in combination with Neoral (R) (cyclosporine, USP MODIFIED) and corticosteroids. The incidence and severity of biopsy-proven acute rejection episodes, graft survival, patient survival, infection rates, laboratory measurements, and adverse events were compared across groups after 6 months of therapy. Results. Among the 103 recipients, patients receiving 1, 2, or 4 mg/day experienced a 32.4%, 14.7%, or 25.7% incidence of biopsy-proven acute rejection episodes within the first 6 months posttransplantation, respectively. Even though the study was mot powered to demonstrate efficacy, the incidence of moderate and severe acute rejection episodes was found to be significantly lower among patients in the 2 mg and 4 mg/day groups than in the 1 mg/day group (P=0.002 and P=0.006, respectively). Overall graft and patient survival rates were excellent. RAD was generally well tolerated. Although blood lipid levels increased in all groups, changes were manageable with lipid-lowering agents and did not warrant discontinuation of study medication. The incidence of viral and fungal infections was low; however, it was higher among recipients treated with 4 mg/day, Conclusions. In combination with Neoral (R) and corticosteroids, RAD doses of 2 mg and 4 mg/day resulted in lower rates of acute rejection episodes and efficacy failure than the 1 mg/day dose and were significantly more effective in reducing the severity of rejection. Large-scale, controlled, follow-up studies are currently in progress to confirm these initial findings.
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收藏
页码:1400 / 1406
页数:7
相关论文
共 15 条
  • [1] CHRONIC GRAFT-REJECTION
    AZUMA, H
    TILNEY, NL
    [J]. CURRENT OPINION IN IMMUNOLOGY, 1994, 6 (05) : 770 - 776
  • [2] Steady-state pharmacokinetics and tolerability of RAD and its influence on cyclosporine in stable renal transplant patients
    Dantal, J
    Lehne, G
    Winkler, M
    Hauser, IA
    Lison, AE
    Soulillou, JP
    Budde, K
    Fauchald, P
    Müller, L
    Paradis, K
    Kovarik, JM
    Neumayer, HH
    [J]. TRANSPLANTATION, 1999, 67 (07) : S160 - S160
  • [3] The correlation of Banff scoring with reversibility of first and recurrent rejection episodes
    Gaber, LW
    Schroeder, TJ
    Moore, LW
    ShakouhAmiri, MH
    Gaber, AO
    [J]. TRANSPLANTATION, 1996, 61 (12) : 1711 - 1715
  • [4] TREATMENT WITH RAPAMYCIN AND MYCOPHENOLIC-ACID REDUCES ARTERIAL INTIMAL THICKENING PRODUCED BY MECHANICAL INJURY AND ALLOWS ENDOTHELIAL REPLACEMENT
    GREGORY, CR
    HUANG, XF
    PRATT, RE
    DZAU, VJ
    SHORTHOUSE, R
    BILLINGHAM, ME
    MORRIS, RE
    [J]. TRANSPLANTATION, 1995, 59 (05) : 655 - 661
  • [5] GRINYO J, 1995, LANCET, V345, P1321
  • [6] A phase I study of a 4-week course of SDZ-RAD (RAD) in quiescent cyclosporine-prednisone-treated renal transplant recipients
    Kahan, BD
    Wong, RL
    Carter, C
    Katz, SH
    Von Fellenberg, J
    Van Buren, CT
    Appel-Dingemanse, S
    [J]. TRANSPLANTATION, 1999, 68 (08) : 1100 - 1106
  • [7] Keown P, 1996, TRANSPLANTATION, V61, P1029
  • [8] Morphologic criteria of chronic renal allograft rejection
    Mihatsch, MJ
    Nickeleit, V
    Gudat, F
    [J]. TRANSPLANTATION PROCEEDINGS, 1999, 31 (1-2) : 1295 - 1297
  • [9] Immunosuppression enhances atherogenicity of lipid profile after transplantation
    Quaschning, T
    Mainka, T
    Nauck, M
    Rump, LC
    Wanner, C
    Krämer-Guth, A
    [J]. KIDNEY INTERNATIONAL, 1999, 56 : S235 - S237
  • [10] SDZ RAD, a new rapamycin derivative - Pharmacological properties in vitro and in vivo
    Schuler, W
    Sedrani, R
    Cottens, S
    Haberlin, B
    Schulz, M
    Schuurman, HJ
    Zenke, G
    Zerwes, HG
    Schreier, MH
    [J]. TRANSPLANTATION, 1997, 64 (01) : 36 - 42