Hodson E M, Willis N S, Craig J C
Children's Hospital at Westmead, Centre for Kidney Research, Locked Bag 4001, Westmead, NSW, Australia, 2145.
Cochrane Database Syst Rev. 2008 Jan 23(1):CD002290. doi: 10.1002/14651858.CD002290.pub3.
Eighty to 90% of children with steroid-sensitive nephrotic syndrome (SSNS) have relapses. About half relapse frequently and are at risk of the adverse effects of corticosteroids. Non-corticosteroid immunosuppressive agents are used to prolong periods of remission in these children, however these agents have significant potential adverse effects. Currently there is no consensus as to the most appropriate second line agent in children who are steroid sensitive, but who continue to relapse.
To evaluate the benefits and harms of non-corticosteroid immunosuppressive agents in relapsing SSNS in children.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, EMBASE, reference lists, conference abstracts and contact with known investigators. Search date: September 2007
Randomised controlled trials (RCTs) or quasi-RCTs were included if they compared non-corticosteroid agents with placebo, prednisone or no treatment, different doses and/or durations of the same non-corticosteroid agent, different non-corticosteroid agents.
Two authors independently assessed study quality and extracted data. Statistical analyses were performed using a random effects model and results expressed as relative risk (RR) with 95% confidence intervals (CI).
We identified 26 studies (1173 children). Cyclophosphamide (RR 0.44, 95% CI 0.26 to 0.73) and chlorambucil (RR 0.15, 95% CI 0.02 to 0.95) significantly reduced the relapse risk at six to twelve months compared with prednisone alone. There was no difference in relapse risk at two years between chlorambucil and cyclophosphamide (RR 1.31, 95% CI 0.80 to 2.13). There was no difference at one year between intravenous and oral cyclophosphamide (RR 0.99, 95% CI 0.76 to 1.29). Cyclosporin was as effective as cyclophosphamide (RR 1.07, 95% CI 0.48 to 2.35) and chlorambucil (RR 0.82, 95% CI 0.44 to 1.53) and levamisole (RR 0.43, 95% CI 0.27 to 0.68) was more effective than steroids alone but the effects were not sustained once treatment was stopped. There was no difference in the risk for relapse between mycophenolate mofetil and cyclosporin (RR 5.00, 95% CI 0.68 to 36.66) but CI were large. Mizoribine and azathioprine were no more effective than placebo or prednisone alone in maintaining remission.
AUTHORS' CONCLUSIONS: Eight week courses of cyclophosphamide or chlorambucil and prolonged courses of cyclosporin and levamisole reduce the risk of relapse in children with relapsing SSNS compared with corticosteroids alone. Clinically important differences in efficacy are possible and further comparative studies are still needed.
80%至90%的激素敏感型肾病综合征(SSNS)患儿会复发。约半数患儿频繁复发,面临着皮质类固醇不良反应的风险。非皮质类固醇免疫抑制剂用于延长这些患儿的缓解期,然而这些药物具有显著的潜在不良反应。目前,对于激素敏感但仍持续复发的儿童,哪种二线药物最为合适尚无共识。
评估非皮质类固醇免疫抑制剂对复发性SSNS患儿的益处和危害。
我们检索了Cochrane对照试验中心注册库(CENTRAL)、MEDLINE、EMBASE、参考文献列表、会议摘要,并与知名研究者进行了联系。检索日期:2007年9月
如果随机对照试验(RCT)或半随机对照试验比较了非皮质类固醇药物与安慰剂、泼尼松或不治疗、同一非皮质类固醇药物的不同剂量和/或疗程、不同的非皮质类固醇药物,则纳入研究。
两位作者独立评估研究质量并提取数据。采用随机效应模型进行统计分析,结果以相对风险(RR)及95%置信区间(CI)表示。
我们纳入了26项研究(1173名儿童)。与单独使用泼尼松相比,环磷酰胺(RR 0.44,95% CI 0.26至0.73)和苯丁酸氮芥(RR 0.15,95% CI 0.02至0.95)在6至12个月时显著降低了复发风险。苯丁酸氮芥和环磷酰胺在两年时的复发风险无差异(RR 1.31,95% CI 0.80至2.13)。静脉注射环磷酰胺和口服环磷酰胺在一年时无差异(RR 0.99,95% CI 0.76至1.29)。环孢素与环磷酰胺(RR 1.07,95% CI 0.48至2.35)和苯丁酸氮芥(RR 0.82,95% CI 0.44至1.53)效果相当,左旋咪唑(RR 0.43,95% CI 0.27至0.68)比单独使用类固醇更有效,但一旦停药效果不能持续。霉酚酸酯和环孢素在复发风险上无差异(RR 5.00,95% CI 0.68至36.66),但置信区间较宽。咪唑立宾和硫唑嘌呤在维持缓解方面并不比安慰剂或单独使用泼尼松更有效。
与单独使用皮质类固醇相比,为期8周的环磷酰胺或苯丁酸氮芥疗程以及延长疗程的环孢素和左旋咪唑可降低复发性SSNS患儿的复发风险。疗效可能存在临床重要差异,仍需进一步的比较研究。