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首页> 外文期刊>Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association >Pulse cyclophosphamide inadequately suppresses reoccurrence of minimal change nephrotic syndrome in corticoid-dependent children.
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Pulse cyclophosphamide inadequately suppresses reoccurrence of minimal change nephrotic syndrome in corticoid-dependent children.

机译:脉冲环磷酰胺不足以抑制皮质激素依赖型儿童微小变化肾病综合征的复发。

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BACKGROUND: In minimal change nephrotic syndrome (MNCS), the most common primary nephrotic syndrome in children, approximately 95% of cases show excellent responses to steroid therapy. However, responding patients may become steroid dependent and experience serious side effects. Although oral cyclophosphamide has been recommended in these patients, long-term side effects such as gonadal toxicity are an important concern. Therefore, cyclophosphamide pulses given intravenously may provide an option that maintains remission with less-frequent side effects. METHODS: We treated 20 primary steroid-dependent MCNS patients (15 boys and five girls) with intravenous cyclophosphamide. The patients were children with ages ranging from 3 to 15 years of age. Remission was induced by steroids followed by cyclophosphamide at a dose of 500 mg/m2 body surface area per month for 6 months. During this period, we attempted to completely withdraw steroids and maintain patients on cyclophosphamide alone. We monitored the patients for the occurrence of relapse and side effects during this period and for an additional 6 months after withdrawal of cyclophosphamide. RESULTS: At the end of the 6-month cyclophosphamide treatment period (i.e. 4 months after steroid discontinuation), nine patients (45%) were in remission on cyclophosphamide alone. However, patients that maintained treatment-free remission (cyclophosphamide responders) decreased to five (25%), two (10%) and one (5%) at 6 months, 1 year and 2 years, respectively. CONCLUSION: We found that a 6-month course of pulse cyclophosphamide produced unfavourable effects in the majority of paediatric patients with steroid-dependent nephrotic syndrome.
机译:背景:在儿童最常见的原发性肾病综合征微变化肾病综合征(MNCS)中,大约95%的病例显示出对类固醇治疗的出色反应。但是,有反应的患者可能会成为类固醇依赖者,并会出现严重的副作用。尽管已建议在这些患者中口服环磷酰胺,但长期的副作用(如性腺毒性)是一个重要的问题。因此,静脉给予环磷酰胺脉冲可提供维持缓解且副作用较少的选择。方法:我们用静脉注射环磷酰胺治疗了20名原发性类固醇依赖的MCNS患者(15名男孩和5名女孩)。患者为3至15岁的儿童。甾族化合物随后环磷酰胺以500 mg / m2每月表面积的剂量诱导缓解,持续6个月。在此期间,我们试图完全撤出类固醇并使患者仅接受环磷酰胺治疗。我们在此期间以及戒断环磷酰胺后的另外6个月中监测了患者的复发情况和副作用。结果:在6个月的环磷酰胺治疗期结束时(即类固醇停药后4个月),仅使用环磷酰胺治疗的9名患者(占45%)得以缓解。但是,维持无治疗缓解的患者(环磷酰胺应答者)在6个月,1年和2年时分别降至5(25%),2(10%)和1(5%)。结论:我们发现脉搏环磷酰胺的6个月疗程对大多数患有类固醇依赖型肾病综合征的儿科患者产生不利影响。

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