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他克莫司联合两种不同剂量西罗莫司用于肾移植:一项多中心研究结果

Tacrolimus combined with two different dosages of sirolimus in kidney transplantation: results of a multicenter study.

作者信息

Vitko S, Wlodarczyk Z, Kyllönen L, Czajkowski Z, Margreiter R, Backman L, Perner F, Rigotti P, Jaques B, Abramowicz D, Kessler M, Sanchez-Plumed J, Rostaing L, Rodger R S, Donati D, Vanrenterghem Y

机构信息

Department of Nephrology, IKEM, Prague, Czech Republic.

出版信息

Am J Transplant. 2006 Mar;6(3):531-8. doi: 10.1111/j.1600-6143.2005.01193.x.

Abstract

Tacrolimus combined with mycophenolate mofetil (MMF) is an effective regimen in kidney transplantation. This study compared the efficacy of combining tacrolimus and two different dosages of sirolimus with an established tacrolimus-MMF regimen. Each day in addition to tacrolimus, 325 patients received 2 mg sirolimus (TAC-SRL2 mg), 325 patients received 0.5 mg sirolimus (TAC-SRL0.5 mg) and 327 patients 1 g MMF (TAC-MMF). The initial tacrolimus dose was 0.2 mg/kg/day. Sirolimus patients received loading doses of 6 or 1.5 mg, and daily doses of 2 or 0.5 mg thereafter. Steroid administration was identical for all groups. The incidence of biopsy-proven acute rejection was lower in the TAC-SRL2 mg group (15.7%) compared with the TAC-SRL0.5 mg (25.2%, p = 0.003) and the TAC-MMF groups (22.3%, p = 0.036). Six-month graft survival was 91.0% (TAC-SRL2 mg), 92.6% (TAC-SRL0.5 mg) and 92.4% (TAC-MMF); the respective values for patient survival were 98.1%, 97.8% and 97.9%. Thirty-four patients (10.5%), 19 patients (5.8%) and 16 patients (4.9%) in the TAC-SRL2 mg, TAC-SRL0.5 mg and TAC-MMF groups, respectively, discontinued the study because of adverse events. Hyperlipemia was reported more often in the TAC-SRL2 mg group (24.0%) compared with 19.4% (TAC-SRL0.5 mg) and 11.0% (TAC-MMF; p < 0.05). Combining 2 mg sirolimus/day with tacrolimus results in lower rates of acute rejection, but a higher incidence of adverse events.

摘要

他克莫司联合霉酚酸酯(MMF)是肾移植中的一种有效方案。本研究比较了他克莫司与两种不同剂量西罗莫司联合使用与既定的他克莫司 - MMF方案的疗效。除他克莫司外,每天325例患者接受2mg西罗莫司(TAC - SRL2mg),325例患者接受0.5mg西罗莫司(TAC - SRL0.5mg),327例患者接受1g MMF(TAC - MMF)。他克莫司初始剂量为0.2mg/(kg·天)。接受西罗莫司治疗的患者接受6mg或1.5mg的负荷剂量,此后每日剂量为2mg或0.5mg。所有组的类固醇给药方式相同。经活检证实的急性排斥反应发生率在TAC - SRL2mg组(15.7%)低于TAC - SRL0.5mg组(25.2%,p = 0.003)和TAC - MMF组(22.3%,p = 0.036)。6个月时移植物存活率分别为91.0%(TAC - SRL2mg)、92.6%(TAC - SRL0.5mg)和92.4%(TAC - MMF);患者存活率分别为98.1%、97.8%和97.9%。TAC - SRL2mg组、TAC - SRL0.5mg组和TAC - MMF组分别有34例患者(10.5%)、19例患者(5.8%)和16例患者(4.9%)因不良事件而中断研究。与TAC - SRL0.5mg组(19.4%)和TAC - MMF组(11.0%)相比,TAC - SRL2mg组高脂血症报告更为常见(24.0%;p < 0.05)。每天2mg西罗莫司与他克莫司联合使用导致急性排斥反应发生率较低,但不良事件发生率较高。

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