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首页> 外文期刊>American Journal of Kidney Diseases: The official journal of the National Kidney Foundation >Short-term outcomes of induction therapy with tacrolimus versus cyclophosphamide for active lupus nephritis: A multicenter randomized clinical trial.
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Short-term outcomes of induction therapy with tacrolimus versus cyclophosphamide for active lupus nephritis: A multicenter randomized clinical trial.

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

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摘要

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/m(2) of body surface area, then adjusted to 500-1,000 mg/m(2) 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 (log-transformed) was significantly decreased in tacrolimus- versus intravenous cyclophosphamide-treated patients after the first month of treatment, even with adjustment for baseline proteinuria (protein excretion, 0.01 vs 0.23 g/d; P = 0.02). 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.
机译:背景:环戊酰胺静脉注射泼尼松是治疗狼疮性肾炎的有效方法,但毒性很大。我们比较了他克莫司与静脉内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。地点和参与者:2006年至2008年,来自中国9个肾脏病中心的81例经活检证实为狼疮性肾炎的患者。干预:泼尼松和他克莫司(n = 42)或静脉注射环磷酰胺(n = 39),治疗6个月。他克莫司的起始剂量为0.05 mg / kg / d,并进行滴定以达到5-10 ng / mL的低谷血药浓度。静脉注射环磷酰胺的剂量为体表面积750 mg / m(2),然后每4周调整至500-1,000 mg / m(2),共进行6次脉冲治疗。结果与测量:主要结果为6个月时完全缓解(蛋白尿排泄<0.3 g / 24 h,血清白​​蛋白> / = 3.5 g / dL,尿沉渣正常,血清肌酐水平正常或稳定)。反应(完全或部分缓解),临床指标和不良反应是次要终点。结果:经过6个月的诱导治疗,他克莫司组的完全缓解和缓解的累积概率分别高于静脉注射环磷酰胺组(分别为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,分别为P = 0.2和P = 0.7)。他克莫司治疗的患者与静脉注射环磷酰胺治疗的患者相比,在治疗的第一个月后,蛋白尿(对数转化)显着降低,即使对基线蛋白尿进行了调整(蛋白排泄,0.01 vs 0.23 g / d; P = 0.02)。治疗后,治疗组之间的血清肌酐水平和估计的肾小球滤过率无明显差异。他克莫司组的不良反应如白细胞减少症和胃肠道症状较少。局限性:无盲法,样本量小,随访时间短。结论:与泼尼松联用,他克莫司的诱导疗法在产生狼疮性肾炎完全缓解方面至少与静脉注射环磷酰胺和泼尼松有效,且安全性更高。

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