Komaki Yuga, Komaki Fukiko, Ido Akio, Sakuraba Atsushi
Section of Gastroenterology, Hepatology and Nutrition, Department of Medicine, University of Chicago, Chicago, IL, USA.
Digestive and Lifestyle Diseases, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
J Crohns Colitis. 2016 Apr;10(4):484-94. doi: 10.1093/ecco-jcc/jjv221. Epub 2015 Dec 8.
Approximately 25% of patients with ulcerative colitis [UC] experience a severe flare requiring steroid therapy to avoid colectomy. We performed a systematic review and meta-analysis to assess the efficacy of tacrolimus as a rescue therapy for active UC.
Electronic databases were searched for relevant studies assessing the efficacy of tacrolimus for active UC. Outcomes included short- and long-term clinical response, colectomy free rates, and rate of adverse events in randomised controlled trials [RCTs] and observational studies.
Two RCTs comparing high trough concentration [10-15ng/ml] versus placebo [n = 103] and 23 observational studies [n = 831] were identified. Clinical response at 2 weeks was significantly higher with tacrolimus compared with placebo (risk ratio [RR] = 4.61, 95% confidence interval [CI] = 2.09-10.17, p = 0.15 x 10(-3)] among RCTs. Rates of clinical response at 1 and 3 months were 0.73 [95% CI = 0.64-0.81] and 0.76 [95% CI = 0.59-0.87], and colectomy-free rates remained high at 1, 3, 6, and 12 months [0.86, 0.84, 0.78, and 0.69, respectively] among observational studies. Among RCTs, adverse events were more frequent compared with placebo [RR = 2.01, 95% CI = 1.20-3.37, p = 0.83 x 10(-2)], but there was no difference in severe adverse events [RR = 3.15, 95% CI = 0.14-72.9, p = 0.47]. Severe adverse events were rare among observational studies [0.11, 95% CI = 0.06-0.20].
In the present meta-analysis, tacrolimus was associated with high clinical response and colectomy-free rates without increased risk of severe adverse events for active UC.
约25%的溃疡性结肠炎(UC)患者会经历严重发作,需要接受类固醇治疗以避免结肠切除术。我们进行了一项系统评价和荟萃分析,以评估他克莫司作为活动性UC挽救治疗的疗效。
检索电子数据库,查找评估他克莫司治疗活动性UC疗效的相关研究。结局指标包括随机对照试验(RCT)和观察性研究中的短期和长期临床反应、无结肠切除率以及不良事件发生率。
确定了两项比较高谷浓度(10 - 15ng/ml)与安慰剂(n = 103)的RCT以及23项观察性研究(n = 831)。在RCT中,他克莫司治疗2周时的临床反应显著高于安慰剂(风险比[RR]=4.61,95%置信区间[CI]=2.09 - 10.17,p = 0.15×10⁻³)。观察性研究中,1个月和3个月时的临床反应率分别为0.73(95%CI = 0.64 - 0.81)和0.76(95%CI = 0.59 - 0.87),1、3、6和12个月时的无结肠切除率也维持在较高水平(分别为0.86、0.84、0.78和0.69)。在RCT中,不良事件比安慰剂更常见(RR = 2.01,95%CI = 1.20 - 3.37,p = 0.83×10⁻²),但严重不良事件无差异(RR = 3.15,95%CI = 0.14 - 72.9,p = 0.47)。观察性研究中严重不良事件罕见(0.11,95%CI = 0.06 - 0.20)。
在本荟萃分析中,他克莫司与活动性UC的高临床反应率和无结肠切除率相关,且未增加严重不良事件风险。