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Tacrolimus for ulcerative colitis in children: a multicenter survey in Japan
Tadahiro Yanagi1,2, Kosuke Ushijima1,2, Hidenobu Koga3
1Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Japan.
Insights
Tacrolimus effectively treated pediatric ulcerative colitis in Japan, showing significant steroid-sparing effects. This study confirms its safety and efficacy as a second-line therapy for children with refractory disease.
Area of Science:
- Pediatric Gastroenterology
- Immunosuppressive Therapy
- Inflammatory Bowel Disease Research
Background:
- Limited data exists on tacrolimus effectiveness in pediatric ulcerative colitis.
- Tacrolimus is a known effective treatment for adult refractory ulcerative colitis.
Purpose of the Study:
- To evaluate the effectiveness and safety of tacrolimus for induction and maintenance therapy.
- To assess tacrolimus in Japanese children with ulcerative colitis.
Main Methods:
- Retrospective multicenter survey of 67 pediatric patients (<17 years) treated with tacrolimus.
- Evaluation of disease activity (Pediatric Ulcerative Colitis Activity Index - PUCAI), tacrolimus dosage, outcomes, steroid-sparing effects, and adverse events.
- Clinical remission defined as PUCAI < 10; response as PUCAI reduction ≥ 20 points.
Main Results:
- Short-term clinical remission rate was 47.8%; response rate was 37.3%.
- Significant reduction in prednisolone dose observed (19.2 mg/day to 5.7 mg/day at 8 weeks).
- Adverse event rate was 53.7%, with 6 patients discontinuing therapy.
Conclusions:
- Tacrolimus demonstrated safety and efficacy as a second-line induction therapy.
- Effective for both steroid-dependent and steroid-refractory ulcerative colitis in Japanese children.
- Supports tacrolimus use in pediatric ulcerative colitis management.
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.
Methods:
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.
Results:
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.
Conclusions:
Tacrolimus was a safe and effective second-line induction therapy for steroid-dependent and steroid-refractory ulcerative colitis in Japanese children.
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