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他克莫司与环磷酰胺诱导治疗活动性狼疮肾炎的短期疗效:一项多中心随机临床试验。

Short-term outcomes of induction therapy with tacrolimus versus cyclophosphamide for active lupus nephritis: A multicenter randomized clinical trial.

机构信息

Department of Nephrology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.

出版信息

Am J Kidney Dis. 2011 Feb;57(2):235-44. doi: 10.1053/j.ajkd.2010.08.036. Epub 2010 Dec 21.

Abstract

BACKGROUND

Intravenous cyclophosphamide with prednisone is an effective treatment for lupus nephritis, but with significant toxicities. We compared the efficacy and safety of tacrolimus versus intravenous cyclophosphamide as induction therapy.

STUDY DESIGN

Multicenter noninferiority randomized controlled trial.

SETTING & PARTICIPANTS: 81 patients with biopsy-proven lupus nephritis from 9 nephrology centers in China from 2006-2008.

INTERVENTION

Prednisone and either tacrolimus (n = 42) or intravenous cyclophosphamide (n = 39) for 6 months. Tacrolimus was started at 0.05 mg/kg/d and titrated to achieve a trough blood concentration of 5-10 ng/mL. Intravenous cyclophosphamide was initiated at 750 mg/m² of body surface area, then adjusted to 500-1,000 mg/m² every 4 weeks for a total of 6 pulse treatments.

OUTCOMES & MEASUREMENTS: The primary outcome was complete remission (proteinuria with protein excretion <0.3 g/24 h, serum albumin ≥3.5 g/dL, normal urinary sediment, and normal or stable serum creatinine level) at 6 months. Response (complete or partial remission), clinical parameters, and adverse effects were secondary end points.

RESULTS

After the 6-month induction therapy, the tacrolimus group achieved higher cumulative probabilities of complete remission and response (52.4% vs 38.5% and 90.5% vs 82.1%, respectively) than the intravenous cyclophosphamide group, but differences were not statistically significant (log-rank test, P = 0.2 and P = 0.7, respectively). Proteinuria [corrected] was significantly decreased in tacrolimus- versus intravenous cyclophosphamide-treated patients after the first month of treatment, even with adjustment for baseline proteinuria (protein excretion, 1.76 vs 2.40 g/d; P = 0.02 for the log-transformed analysis). [corrected] After treatment, serum creatinine levels and estimated glomerular filtration rates were not significantly different between treatment groups. Adverse effects, such as leukopenia and gastrointestinal symptoms, were less frequent in the tacrolimus group.

LIMITATIONS

Nonblinded, small sample size, and short duration of follow-up.

CONCLUSIONS

In conjunction with prednisone, induction therapy with tacrolimus is at least as efficacious as intravenous cyclophosphamide and prednisone in producing complete remission of lupus nephritis and has a more favorable safety profile.

摘要

背景

静脉注射环磷酰胺联合泼尼松是治疗狼疮性肾炎的有效方法,但具有显著的毒性。我们比较了他克莫司与静脉注射环磷酰胺作为诱导治疗的疗效和安全性。

研究设计

多中心非劣效性随机对照试验。

研究场所和参与者

2006 年至 2008 年,来自中国 9 个肾脏病中心的 81 例经活检证实的狼疮性肾炎患者。

干预措施

泼尼松联合他克莫司(n=42)或静脉注射环磷酰胺(n=39)治疗 6 个月。他克莫司起始剂量为 0.05mg/kg/d,并滴定至血药谷浓度 5-10ng/ml。静脉注射环磷酰胺起始剂量为 750mg/m2体表面积,然后每 4 周调整剂量至 500-1000mg/m2,共 6 个脉冲治疗。

研究结果

在 6 个月的诱导治疗后,他克莫司组完全缓解(蛋白尿<0.3g/24h,血清白蛋白≥3.5g/dL,尿沉渣正常,血清肌酐水平正常或稳定)的累积概率高于静脉注射环磷酰胺组(52.4% vs. 38.5%和 90.5% vs. 82.1%),但差异无统计学意义(对数秩检验,P=0.2 和 P=0.7)。治疗后第一个月,他克莫司组患者的蛋白尿[校正]明显减少,即使调整了基线蛋白尿(尿蛋白排泄量,1.76 与 2.40g/d;log 转换分析,P=0.02)。治疗后,两组间血清肌酐水平和估计肾小球滤过率无显著差异。他克莫司组的不良反应如白细胞减少和胃肠道症状发生率较低。

局限性

非盲法、样本量小、随访时间短。

结论

与泼尼松合用,他克莫司诱导治疗与静脉注射环磷酰胺加泼尼松一样,能有效诱导狼疮性肾炎完全缓解,且安全性更好。

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