首页> 外文期刊>The Journal of Urology >A placebo controlled study of mycophenolate mofetil used in combination with cyclosporine and corticosteroids for the prevention of acute rejection in renal allograft recipients: 1-year results. The European Mycophenolate Mofetil Cooperative Study Gr
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A placebo controlled study of mycophenolate mofetil used in combination with cyclosporine and corticosteroids for the prevention of acute rejection in renal allograft recipients: 1-year results. The European Mycophenolate Mofetil Cooperative Study Gr

机译:霉酚酸酯与环孢素和皮质类固醇合用预防肾移植患者急性排斥反应的安慰剂对照研究:1年结果。欧洲霉酚酸酯Mofetil合作研究组

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PURPOSE: We performed a randomized, double-blind, multicenter, placebo controlled study to compare the efficacy and safety of 2 oral doses of mycophenolate mofetil with placebo for prevention of acute rejection episodes following first or second cadaveric renal allograft transplantation. MATERIALS AND METHODS: A total of 491 patients were enrolled in the study and randomly allocated to receive placebo (166), 1 gm. mycophenolate mofetil twice daily (165) or 1.5 gm. mycophenolate mofetil twice daily (160). Patients were given concomitant immunosuppression with cyclosporine and corticosteroids. Treatment with mycophenolate mofetil was initiated within 72 hours of transplantation and was continued for at least 1 year. RESULTS: The percentages of patients who experienced biopsy proved rejection or withdrew early from the trial for any reason were significantly reduced with 2 gm. (30.3%) and 3 gm. (38.8%) mycophenolate mofetil compared to placebo (56.0%) (p < 0.001). The biopsy proved rejection rates of the placebo, and 2 gm. and 3 gm. mycophenolate mofetil treatment arms were 46.4, 17.6 and 13.8%, respectively. There were fewer patients in the 2 gm. (28.5%) and 3 gm. (24.4%) mycophenolate mofetil groups compared to the placebo (51.8%) group, who received full courses of corticosteroids or antilymphocyte agents for treatment of rejection episodes in the first 6 months after renal transplantation. There was a greater incidence of gastrointestinal adverse events, leukopenia and opportunistic events in the mycophenolate mofetil treatment groups. CONCLUSIONS: Mycophenolate mofetil was shown to reduce significantly the number of patients who experienced biopsy proved rejection episodes or treatment failure during the first year after renal transplantation, and was well tolerated.
机译:目的:我们进行了一项随机,双盲,多中心,安慰剂对照的研究,比较了2剂口服麦考酚酸酯和安慰剂预防第一次或第二次尸体肾同种异体移植后急性排斥反应的有效性和安全性。材料与方法:本研究共纳入491例患者,随机分配接受1 gm的安慰剂(166)。霉酚酸酯每天两次(165)或1.5克。霉酚酸酯每天两次(160)。给予患者环孢素和皮质类固醇同时免疫抑制。在移植后72小时内开始使用霉酚酸酯进行治疗,并持续至少1年。结果:2 gm显着降低了因任何原因拒绝接受活检或因任何原因从试验中提前退出的活检患者的百分比。 (30.3%)和3克。 (38.8%)霉酚酸酯与安慰剂相比(56.0%)(p <0.001)。活检证实了安慰剂的排斥率为2 gm。和3克霉酚酸酯的治疗组分别为46.4、17.6和13.8%。 2 gm中的患者较少。 (28.5%)和3克。 (24.4%)霉酚酸酯组与安慰剂组(51.8%)相比,安慰剂组在肾移植后的前6个月接受全疗程的皮质类固醇或抗淋巴细胞药物治疗排斥反应。麦考酚酸酯治疗组的胃肠道不良事件,白细胞减少症和机会性事件发生率更高。结论:麦考酚酸酯显着减少了肾移植后第一年经历活检证实排斥反应或治疗失败的患者的数量,并且耐受性良好。

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