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评估多种治疗方法荟萃回归中新药的作用。

Evaluating novel agent effects in multiple-treatments meta-regression.

机构信息

Department of Hygiene and Epidemiology, University of Ioannina School of Medicine, Ioannina, Greece.

出版信息

Stat Med. 2010 Oct 15;29(23):2369-83. doi: 10.1002/sim.4001.

Abstract

Multiple-treatments meta-analyses are increasingly used to evaluate the relative effectiveness of several competing regimens. In some fields which evolve with the continuous introduction of new agents over time, it is possible that in trials comparing older with newer regimens the effectiveness of the latter is exaggerated. Optimism bias, conflicts of interest and other forces may be responsible for this exaggeration, but its magnitude and impact, if any, needs to be formally assessed in each case. Whereas such novelty bias is not identifiable in a pair-wise meta-analysis, it is possible to explore it in a network of trials involving several treatments. To evaluate the hypothesis of novel agent effects and adjust for them, we developed a multiple-treatments meta-regression model fitted within a Bayesian framework. When there are several multiple-treatments meta-analyses for diverse conditions within the same field/specialty with similar agents involved, one may consider either different novel agent effects in each meta-analysis or may consider the effects to be exchangeable across the different conditions and outcomes. As an application, we evaluate the impact of modelling and adjusting for novel agent effects for chemotherapy and other non-hormonal systemic treatments for three malignancies. We present the results and the impact of different model assumptions to the relative ranking of the various regimens in each network. We established that multiple-treatments meta-regression is a good method for examining whether novel agent effects are present and estimation of their magnitude in the three worked examples suggests an exaggeration of the hazard ratio by 6 per cent (2-11 per cent).

摘要

多治疗方法荟萃分析越来越多地用于评估几种竞争方案的相对有效性。在某些随着时间的推移不断引入新药物而不断发展的领域中,在比较旧方案和新方案的试验中,后者的效果可能被夸大了。乐观偏差、利益冲突和其他因素可能是导致这种夸大的原因,但需要在每种情况下对其幅度和影响进行正式评估。虽然在两两荟萃分析中无法识别这种新颖性偏差,但可以在涉及多种治疗方法的试验网络中探索这种偏差。为了评估新药物效果的假设并对其进行调整,我们开发了一种多治疗方法荟萃回归模型,该模型在贝叶斯框架内拟合。当同一领域/专业内有几种针对不同情况且涉及类似药物的多治疗荟萃分析时,可以考虑在每个荟萃分析中存在不同的新药物效果,或者可以考虑在不同情况和结果之间将效果视为可交换的。作为应用,我们评估了在三种恶性肿瘤的化疗和其他非激素全身治疗中对新型药物效应进行建模和调整的影响。我们呈现了结果以及不同模型假设对每个网络中各种方案相对排名的影响。我们确定,多治疗荟萃回归是检查是否存在新型药物效应以及估计其在三个示例中的幅度的一种很好的方法,结果表明危害比夸大了 6%(2-11%)。

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