Berkane Majda, Adarmouch Latifa, Amine Mohamed, Bourrahouat Aicha, Ait Sab Imane, Sbihi Mohamed
Service de pédiatrie B, CHU Mohamed VI, avenue Ibn Sina Amerchich, BP 2360, Marrakech-principal, Maroc.
Département de santé publique, médecine communautaire et épidémiologie, faculté de médecine et de pharmacie de Marrakech, Sidi Abbad, BP 7010, Marrakech 40000, Maroc; Service de recherche clinique et de traitement de l'information médicale, CHU Mohamed VI, avenue Ibn Sina Amerchich, BP 2360, Marrakech-principal, Maroc.
Nephrol Ther. 2018 Apr;14(2):85-90. doi: 10.1016/j.nephro.2017.03.004. Epub 2018 Mar 1.
Cyclophosphamide (CYP) has been used for over 40 years in patients with steroid-sensitive nephrotic syndrome (NSSS) presenting frequent relapses (NSRF) or steroid dependence (NSSD). However, the long-term success of treatment with cyclophosphamide is difficult to predict. The objectives of this study are to determine long-term outcomes of cyclophosphamide and identify the factors associated with sustained remission.
We retrospectively studied the data from 50 patients with idiopathic nephrotic syndrome, treated by oral cyclophosphamide and followed at service of pediatric for more than 8 years for idiopathic nephrotic syndrome and related factors for survival without relapse were evaluated by univariate analysis.
The median age at the time of diagnosis was 4.3 years, and median follow-up time was 1.7 years with the median of 8 years at the first use of CYC. Patients had received a median cumulative dose of 168mg/kg. At the end of follow-up, 38% of patients entered into remission after using CYC while 62% failed to respond and further relapses then occur. The median time of stopping corticosteroid therapy was three month. The survival without relapse was respectively 56% (28 patients), 52% (26 patients), 48% (24 patients), and 38% (19 patients), at 6 months, one year, two years and more than two years. In univariate analysis, the survival without relapse was related to the age at the moment of starting the therapy par CYC (the median was 5 months for an age < 8 years and 41 months for an age≥8 years; P=0.049), the type of nephrotic syndrome [36 months for SNRF, 4 months for NSSD and nephrothic syndrome steroid resistant (NSSR); P=0.068], and the histological lesion (6 months for diffuse mesangial proliferation, 2 months for segmental glomerulosclerosis; P=0.009). The age at the moment of diagnosis, the sex and the cumulative dose of CYC did not have significant influence.
The results presented in this study suggest the use of oral cyclophosphamide for short period remain second line effective therapy. Further well-designed trials are required to evaluate the efficacy of other steroid-sparing agents.
环磷酰胺(CYP)已在频繁复发(NSRF)或激素依赖(NSSD)的激素敏感型肾病综合征(NSSS)患者中使用了40多年。然而,环磷酰胺治疗的长期疗效难以预测。本研究的目的是确定环磷酰胺的长期疗效,并识别与持续缓解相关的因素。
我们回顾性研究了50例特发性肾病综合征患者的数据,这些患者接受口服环磷酰胺治疗,并在儿科随访超过8年,对特发性肾病综合征及无复发生存的相关因素进行单因素分析。
诊断时的中位年龄为4.3岁,中位随访时间为1.7年,首次使用CYC时的中位时间为8年。患者接受的中位累积剂量为168mg/kg。随访结束时,38%的患者在使用CYC后进入缓解期,而62%的患者无反应并随后再次复发。停用皮质类固醇治疗的中位时间为3个月。在6个月、1年、2年和2年以上时,无复发生存分别为56%(28例患者)、52%(26例患者)、48%(24例患者)和38%(19例患者)。在单因素分析中,无复发生存与开始CYC治疗时的年龄有关(年龄<8岁时中位年龄为5个月,年龄≥8岁时为41个月;P=0.049)、肾病综合征类型[SNRF为36个月,NSSD和激素抵抗型肾病综合征(NSSR)为4个月;P=0.068]以及组织学病变(弥漫性系膜增生为6个月,节段性肾小球硬化为2个月;P=0.009)。诊断时的年龄、性别和CYC的累积剂量没有显著影响。
本研究结果表明,短期使用口服环磷酰胺仍是二线有效治疗方法。需要进一步设计完善的试验来评估其他激素替代药物的疗效。