Bumbea Viorica, Kamar Nassim, Ribes David, Esposito Laure, Modesto Anne, Guitard Joelle, Nasou Ghassan, Durand Dominique, Rostaing Lionel
Multiorgan Transplant Unit, University Hospital, Toulouse, France.
Nephrol Dial Transplant. 2005 Nov;20(11):2517-23. doi: 10.1093/ndt/gfh957. Epub 2005 Jun 28.
Switching from calcineurin inhibitors (CNIs) to sirolimus might improve renal function in chronic renal transplant patients.
In a prospective study, we assessed long-term efficacy and safety parameters in 43 renal transplant recipients who were switched from a CNI (cyclosporin A, 65%; and tacrolimus, 35%) to sirolimus for either chronic allograft dysfunction (n = 38) or recurrent cutaneous cancers (n = 5). A kidney biopsy was done in 79% of patients prior to conversion, and showed either chronic allograft nephropathy (n = 26) or CNI nephrotoxicity (n = 7). Conversion was either abrupt or progressive, with CNI withdrawal over 3 weeks. All patients also received steroids with or without mycophenolate mofetil or azathioprin. Patient data were recorded at baseline (D0), at 1 (D30) and 6 months (D180), and at 1, 1.5 and 2 years post-conversion.
After a mean post-conversion follow-up of 27+/-1.5 months, 58% of the patients were still on sirolimus. The survival of intent to treat patients and grafts was 95.3 and 93%, respectively. Overall, there was significant improvement in renal function, creatinine clearance increasing from 49.4+/-14.9 to 53+/-16.3 ml/min at D30 (P = 0.01), and to 54.7+/-20 ml/min at D180 (P = 0.01). Thereafter, creatinine clearance was not different from baseline, i.e. 54.7+/-21.7, 52.8+/-20 and 51.7+/-20.3 ml/min at years 1, 1.5 and 2, respectively. We divided the patients into two groups: responders (n = 29), those with an increase in creatinine clearance at 6 months post-conversion compared with D0, and non-responders (n = 14), those with a decrease in creatinine clearance at 6 months post-conversion compared with D0. In univariate analysis, factors predictive of response included proteinuria at D0 and the magnitudes of the differences between D30 and D0 for serum creatinine and lactate dehydrogenase. The conversion was associated with (i) significant decreases in serum calcium, phosphorus and uric acid, and in haemoglobin levels; (ii) significant increases in serum alkaline phosphatase, total cholesterol, parathyroid hormone, and the number of patients on statin and recombinant erythropoietin therapies; and (iii) the appearance of de novo proteinuria of >1 g/day in 28% of patients (P < 0.0009), which was >2 g/day in 12% of the entire cohort. Kidney biopsies in 17 patients 2 years after conversion showed the same Banff scores as observed at baseline. We identified three independent predictive factors for a renal response to the switch: absence of proteinuria, presence of antihypertensive therapy at D0 and serum lactate dehydrogenase level at D30.
Conversion from CNIs to sirolimus in renal transplant patients with chronic allograft nephropathy was associated with improved renal function; however, 33% of the patients developed overt proteinuria.
对于慢性肾移植患者,从钙调神经磷酸酶抑制剂(CNIs)转换为西罗莫司可能会改善肾功能。
在一项前瞻性研究中,我们评估了43例肾移植受者的长期疗效和安全性参数,这些患者因慢性移植物功能障碍(n = 38)或复发性皮肤癌(n = 5)从一种CNI(环孢素A,65%;他克莫司,35%)转换为西罗莫司。79%的患者在转换前进行了肾活检,结果显示为慢性移植物肾病(n = 26)或CNI肾毒性(n = 7)。转换方式为突然转换或逐步转换,CNI在3周内停用。所有患者还接受了类固醇治疗,部分患者联合使用霉酚酸酯或硫唑嘌呤。在基线(D0)、1个月(D30)、6个月(D180)以及转换后1年、1.5年和2年记录患者数据。
转换后平均随访27±1.5个月,58%的患者仍在服用西罗莫司。意向性治疗患者和移植物的生存率分别为95.3%和93%。总体而言,肾功能有显著改善,肌酐清除率在D30时从49.4±14.9增至53±16.3 ml/min(P = 0.01),在D180时增至54.7±20 ml/min(P = 0.01)。此后,肌酐清除率与基线无差异,即在转换后1年、1.5年和2年时分别为54.7±21.7、52.8±20和51.7±20.3 ml/min。我们将患者分为两组:反应者(n = 29),即转换后6个月时肌酐清除率较D0升高的患者;无反应者(n = 14),即转换后6个月时肌酐清除率较D0降低的患者。单因素分析显示,预测反应的因素包括D0时的蛋白尿以及D30与D0之间血清肌酐和乳酸脱氢酶的差值大小。转换与以下情况相关:(i)血清钙、磷、尿酸以及血红蛋白水平显著降低;(ii)血清碱性磷酸酶、总胆固醇、甲状旁腺激素以及接受他汀类药物和重组促红细胞生成素治疗的患者数量显著增加;(iii)28%的患者出现新发蛋白尿>1 g/天(P < 0.0009),在整个队列中12%的患者蛋白尿>2 g/天。转换后2年对17例患者进行的肾活检显示Banff评分与基线时相同。我们确定了三个独立的预测肾反应的因素:无蛋白尿、D0时接受抗高血压治疗以及D30时的血清乳酸脱氢酶水平。
慢性移植物肾病的肾移植患者从CNIs转换为西罗莫司与肾功能改善相关;然而,33%的患者出现明显蛋白尿。