Leeds Gastroenterology Institute, St. James's University Hospital, Leeds, West Yorkshire LS9 7TF, United Kingdom.
World J Gastroenterol. 2013 Feb 21;19(7):1091-7. doi: 10.3748/wjg.v19.i7.1091.
To suggest infliximab (IFX) is effective for acute severe ulcerative colitis, from real-life clinical practice.
All patients receiving IFX for the treatment of acute severe ulcerative colitis in a single centre were included. Data were extracted from clinical records in order to assess response to IFX therapy. The primary endpoint was colectomy-free survival, and secondary outcomes included glucocorticosteroid-free remission and safety, which was evaluated by recording deaths and adverse events. Demographic and clinical characteristics of those who underwent colectomy and those who were colectomy-free, both at discharge from their index admission, and during follow-up after an initial response to IFX were compared.
Forty-four patients (16 females, mean age 36 years) received IFX between May 2006 and January 2012 for acute severe ulcerative colitis. The median duration of follow-up post-first infusion was 396 d (interquartile range = 173-828 d). There were 21 (47.7%) patients with < 1 year of follow-up, 10 (22.7%) with 1 years to 2 years of follow-up, and 13 (29.5%) with > 2 years of follow-up post-first infusion of IFX. Overall, 35 (79.5%) responded to IFX, avoiding colectomy during their index admission, 29 (65.9%) were colectomy-free at last point of follow-up (median follow-up 396 d), and 25 (56.8%) were in glucocorticosteroid-free remission at end of follow-up. There was one death from post-operative sepsis, 20 d after a single IFX infusion. Colectomy rates were generally lower among those "bridging" to thiopurine. Of 18 patients "bridged" to thiopurine therapy, 17 (94.4%) were colectomy-free, and 15 (83.3%) were in glucocorticosteroid-free remission at study end. No predictors of response were identified.
IFX is effective for acute severe ulcerative colitis in real-life clinical practice. Two-thirds of patients avoided colectomy, and more than 50% were in glucocorticosteroid-free remission.
从真实临床实践中表明英夫利昔单抗(IFX)对急性重度溃疡性结肠炎有效。
所有在单一中心接受 IFX 治疗急性重度溃疡性结肠炎的患者均被纳入研究。从临床记录中提取数据以评估 IFX 治疗的反应。主要终点是免于结肠切除术的生存,次要结局包括无糖皮质激素缓解和安全性,通过记录死亡和不良事件进行评估。比较那些在出院时和在初始 IFX 反应后随访期间行结肠切除术和免于结肠切除术的患者的人口统计学和临床特征。
44 例患者(16 例女性,平均年龄 36 岁)在 2006 年 5 月至 2012 年 1 月期间因急性重度溃疡性结肠炎接受 IFX 治疗。首次输注后中位随访时间为 396 天(四分位距=173-828 天)。21 例(47.7%)患者随访时间<1 年,10 例(22.7%)随访时间为 1-2 年,13 例(29.5%)随访时间>2 年。总体而言,35 例(79.5%)患者对 IFX 有反应,在住院期间免于结肠切除术,29 例(65.9%)在最后一次随访时免于结肠切除术(中位随访 396 天),25 例(56.8%)在随访结束时无糖皮质激素缓解。单次 IFX 输注后 20 天,1 例患者因术后脓毒症死亡。在接受硫唑嘌呤“桥接”治疗的患者中,结肠切除术的发生率通常较低。在 18 例接受硫唑嘌呤“桥接”治疗的患者中,17 例(94.4%)免于结肠切除术,15 例(83.3%)在研究结束时无糖皮质激素缓解。未发现反应的预测因素。
IFX 在真实临床实践中对急性重度溃疡性结肠炎有效。三分之二的患者免于结肠切除术,超过 50%的患者无糖皮质激素缓解。