Yan H L, Zong H T, Cui Y S, Li N, Zhang Y
Urology Department, Beijing Tian-Tan Hospital, Capital Medical University, Beijing, China.
Urology Department, Beijing Tian-Tan Hospital, Capital Medical University, Beijing, China.
Transplant Proc. 2014 Jun;46(5):1302-13. doi: 10.1016/j.transproceed.2014.02.010.
Many studies have compared the safety and efficacy of the calcineurin inhibitor (CNI) avoidance or CNI withdrawal regimens with typical CNI regimens, but the results remain controversial. The aim of this systematic review and meta-analysis is to make a profound review and an objective appraisal of the safety and efficacy of the CNI avoidance and CNI withdrawal protocols.
We searched PUBMED, EMBASE, and the reference lists of retrieved studies to identify randomized controlled trials (RCTs) that referred to CNI-free regimens, CNI avoidance, or CNI withdrawal for kidney transplantation. Eight publications involving 27 different RCTs and a total of 3953 patients were used in the analysis.
Use of mammalian target of rapamycin inhibitors, namely sirolimus (SRL), in combination with mycophenolate, conserve graft function at 1 year (glomerular filtration rage [GFR]: mean difference MD 6.21, 95% CI 0.02-12.41, P = .05; serum creatinine: MD -0.11, 95% CI -0.19 to -0.03, P = .01, respectively) and 2 years post-transplant (GFR: MD 13.96, 95% CI 7.32-20.60, P < .0001). Similarly, early withdrawal (≤ 6 months) of CNIs protect graft function at 1 year after transplant (GFR: MD 7.03, 95% CI 4.84-9.23, P < .00001, serum creatinine: MD -0.21, 95% CI -0.22 to -0.19, P < .00001, respectively). CNI avoidance and withdrawal strategies are associated with higher incidence of acute rejection at 1 year post-transplant (odds ratio OR 1.74, 95% CI 1.08-2.81, P = .02; OR 1.78, 95% CI 1.35-2.34, P < .0001, respectively). At 2 years after transplant, there was no significant difference (OR 0.92, 95% CI 0.33-2.51, P = .86; OR 2.42, 95% CI 1.01-5.82, P = .05, respectively). Meanwhile, neither adverse events nor patient/graft survival differed significantly between the CNI-free and CNI protocols at 1 and 2 years. Referring to long-term results in the published RCTs, use of CNI-free and CNI withdrawal regimens achieve better renal function vs CNI regimens, with no significant difference in patient and graft survival, acute rejection, and most reported adverse events.
In conclusion, this systematic review and meta-analysis suggests that renal recipients with early withdrawal of CNI drugs or avoiding CNI with SRL perform better to conserve graft function at 1 and 2 years post-transplant. Though the use of CNI regimens performs no better in 2-year acute rejection vs the contrast group, they greatly decrease the incidence of acute rejection at the first year after transplantation. CNI avoidance and withdrawal regimens improve the long-term renal function and perform similarly in the acute rejection, patient and graft survival, and adverse events. Due to the limited amounts of long-term studies, more high-quality RCTs are needed.
许多研究比较了钙调神经磷酸酶抑制剂(CNI)避免使用或CNI撤药方案与典型CNI方案的安全性和有效性,但结果仍存在争议。本系统评价和荟萃分析的目的是对CNI避免使用和CNI撤药方案的安全性和有效性进行深入回顾和客观评估。
我们检索了PUBMED、EMBASE以及检索到的研究的参考文献列表,以确定提及肾移植无CNI方案、CNI避免使用或CNI撤药的随机对照试验(RCT)。分析中使用了涉及27项不同RCT且共3953例患者的8篇出版物。
使用雷帕霉素哺乳动物靶点抑制剂,即西罗莫司(SRL),联合霉酚酸,在移植后1年(肾小球滤过率[GFR]:平均差值MD 6.21,95%可信区间CI 0.02 - 12.41,P = 0.05;血清肌酐:MD -0.11,95%CI -0.19至 -0.03,P = 0.01)和2年时(GFR:MD 13.96,95%CI 7.32 - 20.60,P < 0.0001)可保留移植肾功能。同样,早期(≤6个月)停用CNI可在移植后1年保护移植肾功能(GFR:MD 7.03,95%CI 4.84 - 9.23,P < 0.00001;血清肌酐:MD -0.21,95%CI -0.22至 -0.19,P < 0.00001)。CNI避免使用和撤药策略与移植后1年急性排斥反应的较高发生率相关(比值比OR 1.74,95%CI 1.08 - 2.81,P = 0.02;OR 1.78,95%CI 1.35 - 2.34,P < 0.0001)。在移植后2年,无显著差异(OR 0.92,95%CI 0.33 - 2.51,P = 0.86;OR 2.42,95%CI 1.01 - 5.82,P = 0.05)。同时,在1年和2年时,无CNI方案与CNI方案之间的不良事件、患者/移植物存活率均无显著差异。参考已发表RCT的长期结果,与CNI方案相比,使用无CNI和CNI撤药方案可实现更好的肾功能,在患者和移植物存活率、急性排斥反应以及大多数报告的不良事件方面无显著差异。
总之,本系统评价和荟萃分析表明,早期停用CNI药物或使用SRL避免使用CNI的肾移植受者在移植后1年和2年保护移植肾功能方面表现更好。虽然在2年急性排斥反应方面,CNI方案与对照组相比并无优势,但它们在移植后第一年大大降低了急性排斥反应的发生率。CNI避免使用和撤药方案改善了长期肾功能,在急性排斥反应、患者和移植物存活率以及不良事件方面表现相似。由于长期研究数量有限,需要更多高质量的RCT。