Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Inflamm Bowel Dis. 2012 May;18(5):803-8. doi: 10.1002/ibd.21853. Epub 2011 Sep 1.
We report a multicenter study of oral tacrolimus (FK506) therapy in steroid-refractory ulcerative colitis (UC).
In a placebo-controlled, double-blind study, 62 patients with steroid-refractory, moderate-to-severe UC were randomized into either a tacrolimus group or a placebo for 2 weeks. Patients were evaluated using the Disease Activity Index (DAI). As an entry criterion, patients had to have a total DAI score of 6 or more as well as a mucosal appearance subscore of 2 or 3. Clinical response was defined as improvement in all DAI subscores. Mucosal healing was defined as mucosal appearance subscore of 0 or 1. Clinical remission was defined as a total DAI score ≤ 2 with an individual subscore of 0 or 1.
The mean total DAI score at study entry was 9.8 ± 1.61 in the tacrolimus group and 9.1 ± 1.05 in the placebo group. At week 2 the clinical response rate was 50.0% (16/32) in the tacrolimus group and 13.3% (4/30) in the placebo group (P = 0.003). The rate of mucosal healing observed was 43.8% (14/32) in the tacrolimus group and 13.3% (4/30) in the placebo group (P = 0.012) and the rate of clinical remission observed was 9.4% (3/32) in the tacrolimus group and 0.0% (0/30) in the placebo group (P = 0.238). The therapies in this study were well tolerated, with only minor side effects.
Oral tacrolimus therapy in patients with steroid-refractory UC shortened the acute phase and induced rapid mucosal healing. These results suggest that tacrolimus therapy is useful as an alternative therapy for steroid-refractory UC.
我们报告了一项多中心研究,评估了口服他克莫司(FK506)治疗类固醇难治性溃疡性结肠炎(UC)的效果。
在一项安慰剂对照、双盲研究中,62 例类固醇难治性、中重度 UC 患者被随机分为他克莫司组或安慰剂组,治疗 2 周。采用疾病活动指数(DAI)评估患者。入组标准为 DAI 总分≥6 分,黏膜表现亚评分≥2 分或≥3 分。临床缓解定义为所有 DAI 亚评分均改善。黏膜愈合定义为黏膜表现亚评分 0 或 1。临床缓解定义为 DAI 总分≤2 分,且各单项评分均为 0 或 1。
他克莫司组和安慰剂组患者入组时的平均 DAI 总分分别为 9.8±1.61 和 9.1±1.05。第 2 周末,他克莫司组的临床缓解率为 50.0%(16/32),安慰剂组为 13.3%(4/30)(P=0.003)。他克莫司组黏膜愈合率为 43.8%(14/32),安慰剂组为 13.3%(4/30)(P=0.012);他克莫司组临床缓解率为 9.4%(3/32),安慰剂组为 0.0%(0/30)(P=0.238)。该研究中的治疗方法耐受性良好,仅有轻微不良反应。
口服他克莫司治疗类固醇难治性 UC 可缩短急性期并诱导快速黏膜愈合。这些结果表明,他克莫司治疗可能是类固醇难治性 UC 的一种有效替代治疗方法。