Tabibzadeh Nahid, Glowacki François, Frimat Marie, Elsermans Vincent, Provôt François, Lionet Arnaud, Gnemmi Viviane, Hertig Alexandre, Noël Christian, Hazzan Marc
CHU Lille - Service de Néphrologie - F-59000 Lille, France.
Université de Lille - UMR 995, F-59000 Lille, France.
Clin Transplant. 2016 Nov;30(11):1480-1487. doi: 10.1111/ctr.12843. Epub 2016 Oct 13.
Despite long-term side effects, calcineurin inhibitors (CNI) remain a cornerstone of immunosuppression in renal transplantation. Few trials assessed the long-term outcome after early CNI withdrawal.
This intention-to-treat study assessed the 10-year outcome of 108 patients randomly converted from a cyclosporine (CsA)-mycophenolate mofetil (MMF)-prednisone regimen to a dual therapy (CsA-prednisone or MMF-prednisone) at 3 months postgraft.
At 10 years, 3.7% in the CsA group and 35.2% in the MMF group remained on the protocol regimen (P<.001). eGFR was higher in the MMF group (64.4±21 vs 49.7±14.7 mL/min/1.73 m², P<.001), although acute rejection (12 vs 4 in the CsA group, P=.03) and Class II DSA incidences were increased. CNI-related toxicity (P=.019) and moderate-to-severe IF/TA (P=.004) were higher in the CsA group. Ten-year graft and patient survivals were not different. In multivariate analysis, acute rejection remained the strongest predictor of graft loss (HR=11.64, 95% CI [5.05-26.79], P<.0001).
MMF withdrawal largely failed due to CNI toxicity, while CsA withdrawal led to increased graft failure due to uncontrolled acute rejection without increasing graft survival. From this study, it remains unclear which patients could benefit from limiting CNI exposure.
尽管存在长期副作用,但钙调神经磷酸酶抑制剂(CNI)仍是肾移植免疫抑制的基石。很少有试验评估早期停用CNI后的长期结局。
这项意向性治疗研究评估了108例患者在移植后3个月从环孢素(CsA)-霉酚酸酯(MMF)-泼尼松方案随机转换为双联疗法(CsA-泼尼松或MMF-泼尼松)后的10年结局。
10年后,CsA组3.7%的患者和MMF组35.2%的患者仍采用原方案治疗(P<0.001)。MMF组的估算肾小球滤过率(eGFR)更高(64.4±21对49.7±14.7 mL/min/1.73 m²,P<0.001),尽管急性排斥反应发生率(CsA组12例对4例,P=0.03)和Ⅱ类供者特异性抗体(DSA)发生率有所增加。CsA组的CNI相关毒性(P=0.019)和中重度间质纤维化/肾小管萎缩(IF/TA)(P=0.004)更高。10年的移植物和患者生存率无差异。多变量分析中,急性排斥反应仍然是移植物丢失的最强预测因素(风险比[HR]=11.64,95%置信区间[CI][5.05-26.79],P<0.0001)。
由于CNI毒性,停用MMF大多失败,而停用CsA由于急性排斥反应未得到控制导致移植物失败增加,且未提高移植物生存率。从这项研究中,仍不清楚哪些患者可从限制CNI暴露中获益。