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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >Cyclophosphamide in the treatment of focal segmental glomerulosclerosis
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Cyclophosphamide in the treatment of focal segmental glomerulosclerosis

机译:环磷酰胺治疗局灶性节段性肾小球硬化

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Prednisone is the initial treatment of primary focal segmental glomerulosclerosis. However, when immunosuppressive agents in combination with steroids are used in the treatment of prednisone-dependent and prednisone-resistant patients the remission rate is variable. We report a long-term trial using cyclophosphamide (2.0 to 3.0 mg/kg body weight for 12 weeks) in combination with prednisone (1.0 to 2.0 mg/kg body weight), as compared with prednisone alone for the treatment of prednisone-resistant and frequently relapsing nephrotic syndrome and focal segmental glomerulosclerosis. Fifty-four patients (34 males and 20 females) with a diagnosis of idiopathic nephrotic syndrome and focal segmental glomerulosclerosis, followed-up for an average of 86.1 ± 82.4 months, were evaluated. Complete remission occurred in 20.4% and partial remission in 14.8% of the patients treated with steroids and in 26.7 and 20.0% of the patients treated with cyclophosphamide + prednisone, respectively. Of the 24 prednisone-resistant patients treated with steroids in combination with cyclophosphamide, 33.3% obtained a complete/partial response. At the time of final evaluation, 25% of the patients treated with prednisone and 10.0% of those treated with prednisone in combination with cyclophosphamide had reached end-stage renal disease. Persistent nephrotic syndrome and progressive renal insufficiency were more frequently observed among the patients treated with prednisone alone (50.0 vs 33.3% and 33.3 vs 16.7%, respectively). The treatments were well tolerated and no patient experienced adverse reactions requiring discontinuation of medications. Although open-label and non-randomized, the present trial showed that cyclophosphamide is a reasonable choice for the treatment of primary focal segmental glomerulosclerosis and prednisone-resistant nephrotic syndrome.
机译:泼尼松是原发性局灶性节段性肾小球硬化的初始治疗方法。但是,当免疫抑制剂与类固醇联合用于治疗泼尼松依赖性和强的松耐药性患者时,其缓解率是可变的。我们报告了一项长期试验,将环磷酰胺(2.0至3.0 mg / kg体重,为期12周)与泼尼松(1.0至2.0 mg / kg体重)联合使用,与单独使用泼尼松治疗耐泼尼松和经常复发的肾病综合征和局灶性节段性肾小球硬化。评估了54例诊断为特发性肾病综合征和局灶性节段性肾小球硬化症的患者(平均随访时间为86.1±82.4个月)。接受类固醇治疗的患者中,完全缓解率分别为20.4%,部分缓解率为14.8%,而使用环磷酰胺+泼尼松的患者分别为26.7%和20.0%。在接受类固醇与环磷酰胺联合治疗的24例泼尼松耐药患者中,有33.3%获得了完全/部分缓解。在最终评估时,泼尼松治疗的患者中有25%和泼尼松与环磷酰胺联合治疗的患者中有10.0%达到了晚期肾病。在单独使用泼尼松治疗的患者中,持续性肾病综合征和进行性肾功能不全的发生率更高(分别为50.0 vs. 33.3%和33.3 vs vs. 16.7%)。治疗耐受性好,没有患者出现不良反应而需要停药。尽管开放标签和非随机标签,但本试验显示环磷酰胺是治疗原发性局灶性节段性肾小球硬化症和抗泼尼松肾病综合征的合理选择。

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