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甲氨蝶呤用于诱导难治性克罗恩病缓解

Methotrexate for induction of remission in refractory Crohn's disease.

作者信息

Alfadhli A A F, McDonald J W D, Feagan B G

出版信息

Cochrane Database Syst Rev. 2005 Jan 25(1):CD003459. doi: 10.1002/14651858.CD003459.pub2.


DOI:10.1002/14651858.CD003459.pub2
PMID:15674908
Abstract

BACKGROUND: Although corticosteroids are effective for induction of remission of Crohn's disease, approximately 20% of patients who respond relapse when steroids are withdrawn and become steroid dependent (Binder 1985). Furthermore, corticosteroids exhibit significant adverse effects. The success of methotrexate as a treatment for rheumatoid arthritis led to its evaluation in patients with refractory Crohn's disease. Methotrexate has been studied for induction of remission of refractory Crohn's disease and has become the principal alternative to azathioprine/6MP therapy. The evidence for its effectiveness has not been subjected to a systematic review. OBJECTIVES: To conduct a systematic review of the evidence for effectiveness of methotrexate for induction of remission in patients with active Crohn's disease in the presence and absence of concomitant steroid therapy. SEARCH STRATEGY: A computer-assisted search of MEDLINE and EMBASE for relevant studies published in English, French, Spanish, Italian and German between 1966 and July 2004. Manual searches of reference lists from potentially relevant papers were performed to identify additional studies. The Cochrane Controlled Trials Register and the IBD Review Group Specialized Trials Register were also searched. SELECTION CRITERIA: Randomized controlled trials involving patients of age > 17 years with refractory Crohn's disease defined by conventional clinical, radiological and endoscopic criteria, which was categorized as being active (Crohn's disease activity index >150). OUTCOME MEASURES: The outcome measure was the rate of induction of remission and complete withdrawal from steroids in the treatment and control groups after > 16 weeks of treatment. A secondary outcome was induction of remission with reduction in steroid dose of at least 50%. Selection of trials: The results of the searches above were reviewed independently by two observers and relevant studies selected according to the predefined selection criteria. Any disagreement among reviewers was resolved by consensus. The same two reviewers assessed the methodological quality of each trial (details of randomization method, including whether intention-to-treat analysis was possible from the published data, number of patients lost to follow-up, and if a blinded outcome assessment was used). A standard data extraction form was used. Appropriateness of combining results: Trials were first reviewed to assess the clinical comparability of trial protocols and study populations. MAIN RESULTS: Five randomized trials were identified. The five studies differed with respect to participants, intervention, and outcomes to the extent that it was considered to be inappropriate to combine the data statistically. Three small studies which employed low doses of methotrexate orally showed no statistically significant difference between methotrexate and placebo/control medication treated patients. One small study which used a higher dose of intravenous/oral methotrexate showed no statistically significant difference between methotrexate and azathioprine. A larger study which employed a higher dose of methotrexate intramuscularly showed substantial benefit (number needed to treat, NNT=5). Adverse effects were more common with high dose intramuscular methotrexate therapy than with placebo. AUTHORS' CONCLUSIONS: There is evidence from a single large randomized trial on which to recommend the use of methotrexate 25 mg intramuscularly weekly for induction of remission and complete withdrawal from steroids in patients with refractory Crohn's disease. Although adverse effects were more common than with placebo, they were not severe. There is no evidence on which to base a recommendation for use of lower dose oral methotrexate.

摘要

背景:尽管皮质类固醇对诱导克罗恩病缓解有效,但约20%有反应的患者在停用类固醇后复发并变得依赖类固醇(Binder,1985年)。此外,皮质类固醇有显著的不良反应。甲氨蝶呤治疗类风湿关节炎取得成功,促使其在难治性克罗恩病患者中得到评估。甲氨蝶呤已被研究用于诱导难治性克罗恩病缓解,并已成为硫唑嘌呤/6-巯基嘌呤治疗的主要替代方法。其有效性的证据尚未经过系统评价。 目的:对甲氨蝶呤在有或无皮质类固醇联合治疗情况下诱导活动期克罗恩病患者缓解有效性的证据进行系统评价。 检索策略:通过计算机辅助检索MEDLINE和EMBASE,查找1966年至2004年7月期间以英文、法文、西班牙文、意大利文和德文发表的相关研究。对潜在相关论文的参考文献列表进行手工检索以识别其他研究。还检索了Cochrane对照试验注册库和IBD综述小组专门试验注册库。 入选标准:随机对照试验,受试者年龄>17岁,患有根据传统临床、放射学和内镜标准定义的难治性克罗恩病,且分类为活动期(克罗恩病活动指数>150)。 结局指标:结局指标为治疗和对照组治疗16周后诱导缓解和完全停用类固醇的比例。次要结局是诱导缓解且类固醇剂量至少减少50%。试验选择:上述检索结果由两名观察者独立审查,并根据预先确定的入选标准选择相关研究。评审者之间的任何分歧通过协商解决。同两名评审者评估每个试验的方法学质量(随机化方法细节,包括能否从发表数据进行意向性治疗分析、失访患者数量以及是否使用盲法结局评估)。使用标准数据提取表。合并结果的适宜性:首先对试验进行审查,以评估试验方案和研究人群的临床可比性。 主要结果:确定了五项随机试验。这五项研究在参与者、干预措施和结局方面存在差异,以至于认为将数据进行统计学合并不合适。三项口服低剂量甲氨蝶呤的小型研究显示,甲氨蝶呤治疗组与安慰剂/对照药物治疗组之间无统计学显著差异。一项使用较高剂量静脉内/口服甲氨蝶呤的小型研究显示,甲氨蝶呤与硫唑嘌呤之间无统计学显著差异。一项使用较高剂量肌肉注射甲氨蝶呤的大型研究显示有显著益处(治疗所需人数,NNT = 5)。高剂量肌肉注射甲氨蝶呤治疗的不良反应比安慰剂更常见。 作者结论:有一项大型随机试验的证据支持推荐每周肌肉注射25 mg甲氨蝶呤用于诱导难治性克罗恩病患者缓解和完全停用类固醇。尽管不良反应比安慰剂更常见,但并不严重。没有证据支持推荐使用低剂量口服甲氨蝶呤。

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