Hospital Clínic/IDIBAPS, Barcelona, Spain; Centro de Investigación Biomédica en Red en el Área Temática de Enfermedades Hepáticas y Digestivas, Barcelona, Spain.
Gastroenterology. 2013 Oct;145(4):766-74.e1. doi: 10.1053/j.gastro.2013.06.009. Epub 2013 Jun 13.
BACKGROUND & AIMS: A small placebo-controlled trial reported the efficacy of mercaptopurine therapy for children newly diagnosed with Crohn's disease, yet little is known about the efficacy of early thiopurine therapy in adults.
We performed a prospective double-blind trial of adult patients with a recent (<8 weeks) diagnosis of Crohn's disease. Patients were randomly assigned to groups given azathioprine (2.5 mg · kg(-1) · day(-1), n = 68) or placebo (n = 63) at 31 hospitals from February 2006 to September 2009. Corticosteroids but no other concomitant medications were allowed for control of disease activity. The primary measure of efficacy was sustained corticosteroid-free remission.
After 76 weeks of treatment, 30 patients treated with azathioprine (44.1%) and 23 given placebo (36.5%) were in sustained corticosteroid-free remission (difference of 7.6%; 95% confidence interval, -9.2 to 24.4%; P = .48). The rates of relapse (defined as Crohn's Disease Activity Index score >175) and corticosteroid requirements were similar between groups. A post hoc analysis of relapse, defined as a Crohn's Disease Activity Index score >220, showed lower relapse rates in the azathioprine group than in the placebo group (11.8% vs 30.2%; P = .01). Serious adverse events occurred in 14 patients in the azathioprine group (20.6%) and 7 in the placebo group (11.1%) (P = .16). A larger percentage of patients in the azathioprine group had adverse events that led to study drug discontinuation (20.6%) than in the placebo group (6.35%) (P = .02).
In a study of adults with Crohn's disease, early azathioprine therapy was no more effective than placebo to achieve sustained corticosteroid-free remission but was more effective in preventing moderate to severe relapse in a post hoc analysis. EudraCT 2005-001186-34.
一项小规模安慰剂对照试验报道了巯嘌呤治疗新诊断克罗恩病患儿的疗效,但对于早期硫嘌呤治疗成人克罗恩病的疗效知之甚少。
我们对 2006 年 2 月至 2009 年 9 月在 31 家医院就诊的近期(<8 周)诊断为克罗恩病的成年患者进行了前瞻性、双盲试验。患者被随机分为给予硫唑嘌呤(2.5mg·kg(-1)·天(-1),n=68)或安慰剂(n=63)的两组。疾病活动的控制允许使用皮质类固醇,但不允许同时使用其他伴随药物。疗效的主要衡量标准是持续无皮质类固醇缓解。
经过 76 周的治疗,30 名接受硫唑嘌呤治疗的患者(44.1%)和 23 名接受安慰剂治疗的患者(36.5%)处于持续无皮质类固醇缓解状态(差异为 7.6%;95%置信区间,-9.2 至 24.4%;P=0.48)。两组的复发率(定义为克罗恩病活动指数评分>175)和皮质类固醇需求相似。对复发的事后分析(定义为克罗恩病活动指数评分>220)显示,硫唑嘌呤组的复发率低于安慰剂组(11.8%对 30.2%;P=0.01)。硫唑嘌呤组有 14 名患者(20.6%)和安慰剂组有 7 名患者(11.1%)发生严重不良事件(P=0.16)。硫唑嘌呤组因不良事件而停药的患者比例(20.6%)大于安慰剂组(6.35%)(P=0.02)。
在一项成人克罗恩病患者的研究中,早期使用硫唑嘌呤治疗与安慰剂相比,在实现持续无皮质类固醇缓解方面没有更有效,但在事后分析中更有效地预防中重度复发。EudraCT 2005-001186-34。