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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Meta-analysis: remission and response from control arms of randomized trials of biological therapies for active luminal Crohn's disease.
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Meta-analysis: remission and response from control arms of randomized trials of biological therapies for active luminal Crohn's disease.

机译:荟萃分析:针对活动性腔型克罗恩氏病的生物疗法的随机试验的对照组的缓解和反应。

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BACKGROUND: Remission and response are the main outcomes to evaluate the efficacy of new treatments for Crohn's disease (CD). AIM: To explain variation of remission and response rates in active luminal CD. METHODS: We studied control patients from trials of biological therapies through articles retrieved by MEDLINE search (from 1997 to 2007) and by bibliography review. Thousand nine hundred and thirteen control patients from 28 trials were identified; data were extracted by three independent observers and pooled by DerSimonian and Laird random effect model; factors influencing remission and clinical response were explored by metaregression for aggregated data. RESULTS: The pooled control rates of remission and response were 17% and 33%, respectively, both with significant heterogeneity among studies (P < 0.0001). At metaregression, the time of primary outcome evaluation was associated with remission, whereas the trial's criteria for defining response and publication year were predictors of response. CDAI score, CRP levels or other clinical variables related with disease activity or concomitant medications were not significant factors. CONCLUSIONS: Populations used as 'add-on' treatment comparator in trials of biological therapies for active luminal CD are poorly characterized and outcomes are heterogeneous. Planning of future trials will require better description of patients and concomitant therapies, blinding of outcome assessors and homogeneous criteria of outcome definition.
机译:背景:缓解和反应是评估克罗恩病(CD)新疗法疗效的主要结果。目的:解释活性腔CD的缓解和反应率的变化。方法:我们通过MEDLINE搜索(从1997年至2007年)和参考书目评论检索的文章,从生物疗法试验中研究了对照患者。从28个试验中识别出119例对照患者;数据由三个独立的观察员提取,并由DerSimonian和Laird随机效应模型合并。通过回归分析探讨了影响缓解和临床反应的因素。结果:缓解和反应的合并控制率分别为17%和33%,在研究之间均存在显着异质性(P <0.0001)。在元回归时,主要结果评估的时间与缓解相关,而定义反应和出版年的试验标准是反应的预测因子。 CDAI评分,CRP水平或其他与疾病活动或伴随用药有关的临床变量不是重要因素。结论:在活动性腔内CD的生物疗法试验中,用作“附加”治疗比较剂的人群表征较差,且结果异质。计划未来的试验将需要对患者及其伴随疗法进行更好的描述,对结果评估者不了解,并且对结果定义采用统一的标准。

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