Nephrology Division, Hospital do Rim - UNIFESP, São Paulo, Brazil.
Urology Division, Hospital do Rim - UNIFESP, São Paulo, Brazil.
Am J Transplant. 2015 Oct;15(10):2655-64. doi: 10.1111/ajt.13327. Epub 2015 May 18.
This study compared the incidence of CMV infection/disease in de novo kidney transplant recipients receiving everolimus or mycophenolate and no CMV pharmacological prophylaxis. We randomized 288 patients to receive a single 3 mg/kg dose of antithymocyte globulin, tacrolimus, everolimus, and prednisone (r-ATG/EVR, n = 85); basiliximab, tacrolimus, everolimus, and prednisone (BAS/EVR, n = 102); or basiliximab, tacrolimus, mycophenolate, and prednisone (BAS/MPS, n = 101). The primary end-point was the incidence of first CMV infection/disease in the intention-to-treat population at 12 months. Patients treated with r-ATG/EVR showed a 90% proportional reduction (4.7% vs. 37.6%, HR 0.10, 95% CI 0.037-0.29; p < 0.001), while those treated with BAS/EVR showed a 75% proportional reduction (10.8% vs. 37.6%, HR 0.25, 95% CI 0.13-0.48; p < 0.001) in the incidence of CMV infection/disease compared to BAS/MPS. There were no differences in the incidence of acute rejection (9.4 vs. 18.6 vs. 15.8%, p = 0.403), wound-healing complications, delayed graft function, and proteinuria. Mean estimated glomerular filtration rate was lower in BAS/EVR (65.7 ± 21.8 vs. 60.6 ± 20.9 vs. 69.5 ± 21.5 ml/min, p = 0.021). In de novo kidney transplant recipients receiving no pharmacological CMV prophylaxis, reduced-dose tacrolimus and everolimus was associated with a significant reduction in the incidence of CMV infection/disease compared to standard tacrolimus dose and mycophenolate (ClinicalTrials.gov NCT01354301).
本研究比较了接受依维莫司或霉酚酸酯而无 CMV 药物预防的初发肾移植受者中 CMV 感染/疾病的发生率。我们将 288 例患者随机分为三组,分别接受单次 3mg/kg 剂量的抗胸腺细胞球蛋白、他克莫司、依维莫司和泼尼松(r-ATG/EVR,n=85);巴利昔单抗、他克莫司、依维莫司和泼尼松(BAS/EVR,n=102);或巴利昔单抗、他克莫司、霉酚酸酯和泼尼松(BAS/MPS,n=101)。主要终点是意向治疗人群在 12 个月时首次发生 CMV 感染/疾病的发生率。r-ATG/EVR 治疗组的患者发生 CMV 感染/疾病的比例降低了 90%(4.7%比 37.6%,HR 0.10,95%CI 0.037-0.29;p<0.001),而 BAS/EVR 治疗组的患者降低了 75%(10.8%比 37.6%,HR 0.25,95%CI 0.13-0.48;p<0.001),与 BAS/MPS 相比。三组之间 CMV 感染/疾病发生率无差异(9.4%比 18.6%比 15.8%,p=0.403)、急性排斥反应发生率、伤口愈合并发症、延迟移植物功能和蛋白尿发生率。BAS/EVR 组平均估计肾小球滤过率较低(65.7±21.8 比 60.6±20.9 比 69.5±21.5ml/min,p=0.021)。在未接受 CMV 药物预防的初发肾移植受者中,与标准剂量他克莫司和霉酚酸酯相比,低剂量他克莫司和依维莫司可显著降低 CMV 感染/疾病的发生率(ClinicalTrials.gov NCT01354301)。