Yanagi Tadahiro, Ushijima Kosuke, Koga Hidenobu, Tomomasa Takeshi, Tajiri Hitoshi, Kunisaki Reiko, Isihige Takashi, Yamada Hiroyuki, Arai Katsuhiro, Yoden Atsushi, Aomatsu Tomoki, Nagata Satoru, Uchida Keiichi, Ohtsuka Yoshikazu, Shimizu Toshiaki
Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Japan.
Members of the Japanese Society for Pediatric Inflammatory Bowel Disease Working Group, Japan.
Intest Res. 2019 Oct;17(4):476-485. doi: 10.5217/ir.2019.00027. Epub 2019 Aug 31.
BACKGROUND/AIMS: Tacrolimus is effective for refractory ulcerative colitis in adults, while data for children is sparse. We aimed to evaluate the effectiveness and safety of tacrolimus for induction and maintenance therapy in Japanese children with ulcerative colitis.
We retrospectively reviewed the multicenter survey data of 67 patients with ulcerative colitis aged < 17 years treated with tacrolimus between 2000 and 2012. Patients' characteristics, disease activity, Pediatric Ulcerative Colitis Activity Index (PUCAI) score, initial oral tacrolimus dose, short-term (2-week) and long-term (1-year) outcomes, steroid-sparing effects, and adverse events were evaluated. Clinical remission was defined as a PUCAI score < 10; treatment response was defined as a PUCAI score reduction of ≥ 20 points compared with baseline.
Patients included 35 boys and 32 girls (median [interquartile range] at admission: 13 [11-15] years). Thirty-nine patients were steroid-dependent and 26 were steroidrefractory; 20 had severe colitis and 43 had moderate colitis. The initial tacrolimus dose was 0.09 mg/kg/day (range, 0.05-0.12 mg/kg/day). The short-term clinical remission rate was 47.8%, and the clinical response rate was 37.3%. The mean prednisolone dose was reduced from 19.2 mg/day at tacrolimus initiation to 5.7 mg/day at week 8 (P< 0.001). The adverse event rate was 53.7%; 6 patients required discontinuation of tacrolimus therapy.
Tacrolimus was a safe and effective second-line induction therapy for steroid-dependent and steroid-refractory ulcerative colitis in Japanese children.
背景/目的:他克莫司对成人难治性溃疡性结肠炎有效,但儿童相关数据较少。我们旨在评估他克莫司对日本溃疡性结肠炎患儿诱导缓解和维持治疗的有效性及安全性。
我们回顾性分析了2000年至2012年间接受他克莫司治疗的67例年龄小于17岁的溃疡性结肠炎患儿的多中心调查数据。评估了患儿的特征、疾病活动度、儿童溃疡性结肠炎活动指数(PUCAI)评分、初始口服他克莫司剂量、短期(2周)和长期(1年)结局、激素节省效应及不良事件。临床缓解定义为PUCAI评分<10;治疗反应定义为与基线相比PUCAI评分降低≥20分。
患儿包括35名男孩和32名女孩(入院时中位年龄[四分位间距]:13[11 - 15]岁)。39例患儿依赖激素,26例激素抵抗;20例为重症结肠炎,43例为中度结肠炎。他克莫司初始剂量为0.09mg/kg/天(范围:0.05 - 0.12mg/kg/天)。短期临床缓解率为47.8%,临床反应率为37.3%。泼尼松龙平均剂量从开始使用他克莫司时的19.2mg/天降至第8周时的5.7mg/天(P<0.001)。不良事件发生率为53.7%;6例患儿需要停用他克莫司治疗。
他克莫司是日本儿童激素依赖型和激素抵抗型溃疡性结肠炎安全有效的二线诱导治疗药物。