Pediatric Nephrology Department, Assistance Publique-Hôpitaux de Paris, Université Paris 7, Hôpital Robert Debré, Paris, France.
Pediatr Nephrol. 2011 Jun;26(6):927-32. doi: 10.1007/s00467-011-1830-0. Epub 2011 Mar 12.
In order to determine the long-term effects of cyclophosphamide (CPO) and to identify parameters associated with sustained remission, we retrospectively studied the data from 90 patients with steroid-dependent nephrotic syndrome (SDNS) who received a single course of oral cyclophosphamide (2 mg/kg/day for 10 to 12 weeks). The median follow-up period after CPO was 5.5 years (interquartile range 3.2-8.5). Sustained remission reached the cumulative rate of 57% at 1 year, 42% at 2 years, and 31% at 5 years. For the patients who relapsed, the median threshold dose of prednisone between CPO initiation and first relapse has significantly decreased (22.1 mg/kg/day versus 4.9 mg/kg/day, p < 0.001). No further immunosuppressive agent was required in 60% of all patients. Young age at CPO initiation was associated with a lower rate of sustained remission (p < 0.001). Age at diagnosis of nephrotic syndrome, gender, cumulative dose of CPO (in mg/kg), and level of steroid dependence at CPO initiation did not influence the outcome. The incidence of side effects was low. These findings suggest that despite the wide use of new immunosuppressive agents, a short course of CPO remains an effective second-line therapy in SDNS patients. Optimal efficiency was observed in children over 7.5 years.
为了确定环磷酰胺(CPO)的长期效果,并确定与持续缓解相关的参数,我们回顾性研究了 90 例接受单次口服环磷酰胺(2mg/kg/天,持续 10-12 周)治疗的激素依赖性肾病综合征(SDNS)患者的数据。CPO 后中位随访时间为 5.5 年(四分位距 3.2-8.5)。1 年时持续缓解的累积率达到 57%,2 年时为 42%,5 年时为 31%。对于复发的患者,CPO 起始和首次复发之间泼尼松的中位阈值剂量显著降低(22.1mg/kg/天与 4.9mg/kg/天,p<0.001)。在所有患者中,有 60%不需要进一步使用免疫抑制剂。CPO 起始时年龄较小与持续缓解率较低相关(p<0.001)。CPO 起始时的肾病综合征诊断年龄、性别、CPO 累积剂量(mg/kg)和激素依赖性水平均不影响结果。副作用发生率较低。这些发现表明,尽管新的免疫抑制剂广泛应用,但短期 CPO 仍然是 SDNS 患者有效的二线治疗方法。7.5 岁以上的儿童观察到最佳疗效。