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来氟米特与环磷酰胺治疗中国增生型狼疮肾炎患者的诱导缓解:一项随机试验。

Leflunomide versus cyclophosphamide in the induction treatment of proliferative lupus nephritis in Chinese patients: a randomized trial.

机构信息

Department of Nephrology, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.

Department of Nephrology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.

出版信息

Clin Rheumatol. 2019 Mar;38(3):859-867. doi: 10.1007/s10067-018-4348-z. Epub 2018 Nov 13.

Abstract

OBJECTIVES

A prospective, multi-center, randomized controlled study was conducted to evaluate the efficacy and safety of a 24-week course low-dose leflunomide combined with prednisone in the induction treatment of proliferative lupus nephritis in Chinese patients.

METHOD

Patients (n = 100) with biopsy-proved proliferative lupus nephritis were enrolled in this study. They were randomized into two groups and received either leflunomide or cyclophosphamide in conjunction with prednisone for 24 weeks. Leflunomide was given orally with a loading dose of 40 mg/day for 3 days followed by 20 mg/day. Intravenous cyclophosphamide was administered monthly at a dosage of 0.8-1.0 g. The primary efficacy outcome was the frequency of complete remission and partial remission at week 24. The secondary outcomes included changes of urinary protein excretion, serum albumin, complement 3, anti-dsDNA antibody level, and systemic lupus erythematosus disease activity index (SLEDAI) after 24-week therapy.

RESULTS

Of 100 patients, 48 received leflunomide combined with prednisone and other 52 received cyclophosphamide with concomitant prednisone. There were no statistically significant differences between groups in complete remission rate and partial remission rate. At week 24, 23% of patients in the leflunomide group and 27% of patients in the cyclophosphamide group achieved complete remission (P = 0.64), while 56% of patients in the leflunomide group and 42% of patients in the cyclophosphamide group achieved partial remission at week 24 (P = 0.16). SLEDAI, serum albumin, complement 3, anti-dsDNA antibody level, and urinary protein excretion improved significantly in both groups. No significant difference was seen in the changes of clinical parameters after therapy between the two groups. There was no significant difference in side effects in both groups.

CONCLUSIONS

Compared with cyclophosphamide, low-dose leflunomide in combination with prednisone showed both effectiveness and safety in the induction therapy of proliferative lupus nephritis in Chinese patients.

摘要

目的

一项前瞻性、多中心、随机对照研究评估了 24 周低剂量来氟米特联合泼尼松诱导治疗中国患者增生性狼疮肾炎的疗效和安全性。

方法

这项研究纳入了经活检证实的增生性狼疮肾炎患者(n=100)。他们被随机分为两组,分别接受来氟米特或环磷酰胺联合泼尼松治疗 24 周。来氟米特起始剂量 40mg/d,连用 3 天,随后 20mg/d 维持剂量口服。环磷酰胺每月静脉注射 0.8-1.0g。主要疗效终点为第 24 周完全缓解和部分缓解的频率。次要终点包括 24 周治疗后尿蛋白排泄、血清白蛋白、补体 3、抗双链 DNA 抗体水平和系统性红斑狼疮疾病活动指数(SLEDAI)的变化。

结果

100 例患者中,48 例接受来氟米特联合泼尼松治疗,52 例接受环磷酰胺联合泼尼松治疗。两组完全缓解率和部分缓解率无统计学差异。第 24 周时,来氟米特组 23%的患者和环磷酰胺组 27%的患者达到完全缓解(P=0.64),来氟米特组 56%的患者和环磷酰胺组 42%的患者达到部分缓解(P=0.16)。两组患者 SLEDAI、血清白蛋白、补体 3、抗双链 DNA 抗体水平和尿蛋白排泄均明显改善。两组治疗后临床参数的变化无显著差异。两组不良反应发生率无显著差异。

结论

与环磷酰胺相比,低剂量来氟米特联合泼尼松在诱导治疗中国患者增生性狼疮肾炎方面具有有效性和安全性。

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