Wiesel M, Carl S
Department of Urology, University of Heidelberg, Germany.
J Urol. 1998 Jan;159(1):28-33. doi: 10.1016/s0022-5347(01)64000-x.
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.
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.
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.
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.
我们开展了一项随机、双盲、多中心、安慰剂对照研究,以比较两种口服剂量的霉酚酸酯与安慰剂预防首次或第二次尸体肾移植术后急性排斥反应发作的疗效和安全性。
共有491例患者纳入本研究,并随机分配接受安慰剂(166例)、每日两次1克霉酚酸酯(165例)或每日两次1.5克霉酚酸酯(160例)。患者同时接受环孢素和皮质类固醇免疫抑制治疗。霉酚酸酯治疗在移植后72小时内开始,并持续至少1年。
与安慰剂组(56.0%)相比,接受2克(30.3%)和3克(38.8%)霉酚酸酯治疗的患者中,经活检证实发生排斥反应或因任何原因提前退出试验的患者百分比显著降低(p < 0.001)。安慰剂组、2克和3克霉酚酸酯治疗组经活检证实的排斥反应发生率分别为46.4%、17.6%和13.8%。与安慰剂组(51.8%)相比,2克(28.5%)和3克(2�4%)霉酚酸酯组中在肾移植后前6个月因排斥反应发作接受皮质类固醇或抗淋巴细胞药物全疗程治疗的患者较少。霉酚酸酯治疗组胃肠道不良事件、白细胞减少和机会性事件的发生率更高。
霉酚酸酯可显著减少肾移植术后第一年经活检证实发生排斥反应发作或治疗失败的患者数量,且耐受性良好。