Argolini Lorenza Maria, Frontini Giulia, Elefante Elena, Saccon Francesca, Binda Valentina, Tani Chiara, Scotti Isabella, Carli Linda, Gatto Mariele, Esposito Ciro, Gerosa Maria, Caporali Roberto, Doria Andrea, Messa Piergiorgio, Mosca Marta, Moroni Gabriella
Division of Clinical Rheumatology, ASST Istituto Gaetano Pini - CTO, Milan, Italy.
Divisione di Nefrologia e Dialisi-Padiglione Croff, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico Milano, Via della Commenda 15, 20122, Milano, Italy.
J Nephrol. 2021 Apr;34(2):389-398. doi: 10.1007/s40620-020-00753-w. Epub 2020 May 27.
The ideal long-term maintenance therapy of Lupus Nephritis (LN) is still a matter of debate. The present study was aimed at comparing the efficacy/safety profile of cyclosporine (CsA), mycophenolate mofetil (MMF) and azathioprine (AZA) in long-term maintenance therapy of LN.
We performed a retrospective study of patients with biopsy-proven active LN. After induction therapy, all patients received maintenance therapy with CsA, MMF or AZA based on medical decision. Primary endpoint was complete renal remission (CRR) after 8 years (defined as proteinuria < 0.5 g/24 h, eGFR > 60 ml/min/1.73 mq); secondary endpoints were: CRR after 1 year, renal and extrarenal flares, progression of chronic kidney disease (CKD stage 3 or above) and side-effects.
Out of 106 patients, 34 received CsA, 36 MMF and 36 AZA. Clinical and histological characteristics at start of induction therapy were comparable among groups. At start of maintenance therapy, CsA patients had significantly higher proteinuria (P = 0.004) or nephrotic syndrome (P = 0.024) and significantly lower CRR (23.5% vs 55.5% on MMF and 41.7% on AZA, P = 0.024). At one year, CRR was similar in the three groups (79.4% on CsA, 63.8% on MMF, 58.3% on AZA, P = 0.2). At 8 years, the primary endpoint was achieved by 79.4% of CsA vs 83.3% of MMF and 77.8% of AZA patients (P = 0.83); 24 h proteinuria, serum creatinine, eGFR were similar. CKD stage 3 or above developed in 8.8% of CsA, in 8.3% of MMF and in 8.3% of AZA patients (P = 0.92). Flares-free survival curves and incidence of side-effects were not different.
This is the first study comparing CsA, MMF and AZA on long-term LN maintenance therapy. All treatments had similar efficacy in achieving and maintaining CRR, despite more severe baseline clinical features in patients treated with CsA.
狼疮性肾炎(LN)理想的长期维持治疗方案仍存在争议。本研究旨在比较环孢素(CsA)、霉酚酸酯(MMF)和硫唑嘌呤(AZA)在LN长期维持治疗中的疗效/安全性。
我们对经活检证实为活动性LN的患者进行了一项回顾性研究。诱导治疗后,所有患者根据医疗决策接受CsA、MMF或AZA维持治疗。主要终点为8年后的完全肾脏缓解(CRR,定义为蛋白尿<0.5g/24小时,估算肾小球滤过率(eGFR)>60ml/min/1.73m²);次要终点包括:1年后的CRR、肾脏和肾外复发、慢性肾脏病进展(CKD 3期或以上)及副作用。
106例患者中,34例接受CsA治疗,36例接受MMF治疗,36例接受AZA治疗。诱导治疗开始时,各组的临床和组织学特征具有可比性。维持治疗开始时,CsA组患者的蛋白尿(P = 0.004)或肾病综合征(P = 0.024)显著更高,CRR显著更低(CsA组为23.5%,MMF组为55.5%,AZA组为41.7%,P = 0.024)。1年时,三组的CRR相似(CsA组为79.4%,MMF组为63.8%,AZA组为58.3%,P = 0.2)。8年时,CsA组79.4%的患者、MMF组83.3%的患者和AZA组77.8%的患者达到主要终点(P = 0.83);24小时蛋白尿、血清肌酐、eGFR相似。8.8%的CsA组患者、8.3%的MMF组患者和8.3%的AZA组患者发展为CKD 3期或以上(P = 0.92)。无复发生存曲线和副作用发生率无差异。
这是第一项比较CsA、MMF和AZA在LN长期维持治疗中的研究。尽管接受CsA治疗的患者基线临床特征更严重,但所有治疗在实现和维持CRR方面具有相似的疗效。