Gaber A Osama, Kahan Barry D, Van Buren Charles, Schulman Seth L, Scarola Joseph, Neylan John F
Methodist University Hospital, Memphis, TN, USA.
Transplantation. 2008 Nov 15;86(9):1187-95. doi: 10.1097/TP.0b013e318187bab0.
The efficacy and safety of sirolimus (SRL) plus tacrolimus (TAC) versus SRL plus cyclosporine (CsA) were compared in high-risk renal allograft recipients.
Evaluable patients (448) were randomly assigned (1:1) before transplant to receive SRL+TAC or SRL+CsA with corticosteroids. Eligible patients were black and/or repeat transplant recipients, and/or those with high titer of panel-reactive antibodies.
Demographics were similar between groups. Both treatments demonstrated equivalent efficacy of the composite endpoint at 12 months with efficacy failure rates of 21.9% vs. 23.2% (SRL+TAC vs. SRL+CsA, respectively, 95% CI -10.0 to 7.1, P=0.737). Biopsy-confirmed acute rejection rate (13.8% vs. 17.4%) and graft survival rate (89.7% vs. 90.2%) were similar (SRL+TAC vs. SRL+CsA, respectively). In evaluable patients (received at least 1 dose of study drug), renal function (calculated Nankivell glomerular filtration rate) was not superior in SRL+TAC versus SRL+CsA (54.5 vs. 52.6 mL/min, P=0.466); however, in on-therapy patients, glomerular filtration rate was significantly higher in SRL+TAC at most time points. At 12 months, there were no significant differences in rates of death, discontinuation because of adverse events, hypercholesterolemia, hyperlipemia, or proteinuria. Diarrhea and herpes simplex infections occurred significantly more often in SRL+TAC patients. Hypertension, cardiomegaly, increased creatinine, overdose (primarily calcineurin inhibitor toxicity), acne, urinary tract disorders, lymphocele, and ovarian cysts occurred significantly more often in SRL+CsA patients.
This study demonstrated that SRL-based therapy was efficacious in high-risk renal allograft recipients in the first year after transplant, providing equivalent efficacy with CsA or TAC, similar graft survival, low biopsy-confirmed acute rejection rates, excellent renal function, and an acceptable safety profile.
在高风险肾移植受者中比较了西罗莫司(SRL)联合他克莫司(TAC)与SRL联合环孢素(CsA)的疗效和安全性。
可评估患者(448例)在移植前随机分组(1:1),接受SRL+TAC或SRL+CsA联合皮质类固醇治疗。符合条件的患者为黑人及/或再次移植受者,和/或群体反应性抗体滴度高的患者。
两组的人口统计学特征相似。两种治疗方法在12个月时复合终点的疗效相当,疗效失败率分别为21.9%和23.2%(SRL+TAC组与SRL+CsA组,95%CI -10.0至7.1,P=0.737)。活检证实的急性排斥率(13.8%对17.4%)和移植物存活率(89.7%对90.2%)相似(分别为SRL+TAC组与SRL+CsA组)。在可评估患者(接受至少1剂研究药物)中,SRL+TAC组的肾功能(计算的南基韦尔肾小球滤过率)并不优于SRL+CsA组(54.5对52.6 mL/分钟,P=0.466);然而,在治疗中的患者中,SRL+TAC组在大多数时间点的肾小球滤过率显著更高。在12个月时,死亡、因不良事件停药、高胆固醇血症、高脂血症或蛋白尿的发生率没有显著差异。腹泻和单纯疱疹感染在SRL+TAC组患者中发生得更频繁。高血压、心脏肥大、肌酐升高、过量用药(主要是钙调神经磷酸酶抑制剂毒性)、痤疮、泌尿系统疾病、淋巴囊肿和卵巢囊肿在SRL+CsA组患者中发生得更频繁。
本研究表明,基于SRL的治疗方法在移植后第一年对高风险肾移植受者有效,与CsA或TAC疗效相当,移植物存活率相似,活检证实的急性排斥率低,肾功能良好,安全性可接受。