Donia Ahmed Farouk, Ammar Hesham Mohamed, El-Agroudy Amgad El-Baz, Moustafa Fatma El-Husseini, Sobh Mohamed Abdel-Kader
Nephrology Department, Urology and Nephrology Center, Mansoura University, Mansoura, Egypt.
Pediatr Nephrol. 2005 Oct;20(10):1420-5. doi: 10.1007/s00467-005-1943-4. Epub 2005 Jul 27.
Children with steroid-dependent minimal change nephrotic syndrome are prone to serious steroid side effects. Alternative therapies, such as oral cyclophosphamide, may also have serious side effects. We conducted this novel prospective study to compare the long-term efficacies of levamisole and I.V. pulse cyclophosphamide as therapies with potentially fewer side effects. This study included 40 children with idiopathic steroid-dependent minimal change nephrotic syndrome (age 3-15 years; 31 boys and 9 girls). The patients were randomized into two equal groups. One group received levamisole 2.5 mg/kg on alternate days (levamisole group) while the other group received I.V. cyclophosphamide 500 mg/m2/month for six months (cyclophosphamide group). Prednisolone was gradually withdrawn. After stopping treatment, the number of patients that maintained remission was five (25%) in each group at six months, four (20%) versus two (10%) at one year and three (15%) versus one (5%) at two years in the levamisole and cyclophosphamide groups respectively, and one (5%) in each group at three and four years. The overall side effects were mild and both drugs were well tolerated. In view of the results, we recommend trial of levamisole before adopting other therapies with more serious side effects in such patients.
依赖类固醇的微小病变型肾病综合征患儿容易出现严重的类固醇副作用。替代疗法,如口服环磷酰胺,也可能有严重副作用。我们开展了这项新的前瞻性研究,以比较左旋咪唑和静脉脉冲环磷酰胺作为副作用可能较少的疗法的长期疗效。本研究纳入了40例特发性依赖类固醇的微小病变型肾病综合征患儿(年龄3至15岁;31名男孩和9名女孩)。患者被随机分为两组。一组隔日接受2.5mg/kg左旋咪唑(左旋咪唑组),而另一组接受静脉注射环磷酰胺500mg/m²/月,共六个月(环磷酰胺组)。泼尼松龙逐渐减量。停止治疗后,左旋咪唑组和环磷酰胺组在六个月时每组维持缓解的患者人数均为5例(25%),一年时分别为4例(20%)和2例(10%),两年时分别为3例(15%)和1例(5%),三年和四年时每组均为1例(5%)。总体副作用较轻,两种药物耐受性均良好。鉴于研究结果,我们建议在此类患者采用其他副作用更严重的疗法之前先试用左旋咪唑。