Yoshikawa Norishige, Nakanishi Koichi, Sako Mayumi, Oba Mari S, Mori Rintaro, Ota Erika, Ishikura Kenji, Hataya Hiroshi, Honda Masataka, Ito Shuichi, Shima Yuko, Kaito Hiroshi, Nozu Kandai, Nakamura Hidefumi, Igarashi Takashi, Ohashi Yasuo, Iijima Kazumoto
Department of Pediatrics, Wakayama Medical University, Wakayama City, Japan.
Division for Clinical Trials, Clinical Research Center, National Center for Child Health and Development, Tokyo, Japan.
Kidney Int. 2015 Jan;87(1):225-32. doi: 10.1038/ki.2014.260. Epub 2014 Jul 23.
In this multicenter, open-label, randomized controlled trial, we determined whether 2-month prednisolone therapy for steroid-sensitive nephrotic syndrome was inferior or not to 6-month therapy despite significantly less steroid exposure. The primary end point was time from start of initial treatment to start of frequently relapsing nephrotic syndrome. The pre-specified non-inferiority margin was a hazard ratio of 1.3 with one-sided significance of 5%. We randomly assigned 255 children with an initial episode of steroid-sensitive nephrotic syndrome to either 2 - or 6-month treatment of which 246 were eligible for final analysis. The total prednisolone exposure counted both initial and relapse prednisolone treatment administered over 24 months. Median follow-up in months was 36.7 in the 2-month and 38.2 in the 6-month treatment group. Time to frequent relaps was similar in both groups; however, the median was reached only in the 6-month group (799 days). The hazard ratio was 0.86 (90% confidence interval, 0.64-1.16) and met the non-inferior margin. Time to first relapse was also similar in both groups: median day 242 (2-month) and 243 (6-month). Frequency and severity of adverse events were similar in both groups. Most adverse events were transient and occurred during initial or relapse therapy. Thus, 2 months of initial prednisolone therapy for steroid-sensitive nephrotic syndrome, despite less prednisolone exposure, is not inferior to 6 months of initial therapy in terms of time to onset of frequently relapsing nephrotic syndrome.
在这项多中心、开放标签、随机对照试验中,我们确定了对于激素敏感型肾病综合征,尽管泼尼松龙暴露量显著减少,但2个月的泼尼松龙治疗是否劣于6个月的治疗。主要终点是从初始治疗开始至频繁复发肾病综合征开始的时间。预先设定的非劣效性界值为风险比1.3,单侧显著性为5%。我们将255例初发激素敏感型肾病综合征患儿随机分配至2个月或6个月治疗组,其中246例符合最终分析条件。泼尼松龙总暴露量计算了24个月内给予的初始及复发泼尼松龙治疗量。2个月治疗组的中位随访月数为36.7,6个月治疗组为38.2。两组频繁复发的时间相似;然而,仅6个月治疗组达到了中位数(799天)。风险比为0.86(90%置信区间,0.64 - 1.16),符合非劣效界值。两组首次复发时间也相似:中位数分别为第242天(2个月治疗组)和第243天(6个月治疗组)。两组不良事件的频率和严重程度相似。大多数不良事件是短暂的,发生在初始或复发治疗期间。因此,对于激素敏感型肾病综合征,尽管泼尼松龙暴露量较少,但2个月的初始泼尼松龙治疗在频繁复发肾病综合征发病时间方面并不劣于6个月的初始治疗。