School of Computer Science and Statistics, Trinity College Dublin, The University of Dublin, Dublin, Ireland.
National Centre for Pharmacoeconomics, St. James's Hospital, Dublin, Ireland.
Stat Med. 2019 Jun 30;38(14):2505-2523. doi: 10.1002/sim.8139. Epub 2019 Mar 20.
Increasingly, single-armed evidence is included in health technology assessment submissions when companies are seeking reimbursement for new drugs. While it is recognized that randomized controlled trials provide a higher standard of evidence, these are not available for many new agents that have been granted licenses in recent years. Therefore, it is important to examine whether alternative strategies for assessing this evidence may be used. In this work, we examine approaches to incorporating single-armed evidence formally in the evaluation process. We consider matching aggregate level covariates to comparator arms or trials and including this evidence in a network meta-analysis. We consider two methods of matching: (i) we include the chosen matched arm in the data set itself as a comparator for the single-arm trial; (ii) we use the baseline odds of an event in a chosen matched trial to use as a plug-in estimator for the single-arm trial. We illustrate that the synthesis of evidence resulting from such a setup is sensitive to the between-study variability, formulation of the prior for the between-design effect, weight given to the single-arm evidence, and extent of the bias in single-armed evidence. We provide a flowchart for the process involved in such a synthesis and highlight additional sensitivity analyses that should be carried out. This work was motivated by a hepatitis C data set, where many agents have only been examined in single-arm studies. We present the results of our methods applied to this data set.
越来越多的单臂证据被纳入公司为新药寻求报销的卫生技术评估提交材料中。虽然人们认识到随机对照试验提供了更高标准的证据,但对于近年来获得许可的许多新药来说,这些试验并不适用。因此,重要的是要研究是否可以使用替代策略来评估这种证据。在这项工作中,我们研究了在评估过程中正式纳入单臂证据的方法。我们考虑将总体水平协变量与对照臂或试验相匹配,并将该证据纳入网络荟萃分析中。我们考虑了两种匹配方法:(i)我们将所选匹配臂包含在数据集本身中,作为单臂试验的对照;(ii)我们使用所选匹配试验中事件的基线几率作为单臂试验的插件估计值。我们表明,这种设置产生的证据综合结果对研究间变异性、设计效果先验的制定、对单臂证据的重视程度以及单臂证据中的偏差程度很敏感。我们为这种综合所涉及的过程提供了一个流程图,并强调了应该进行的其他敏感性分析。这项工作的动机是来自一个丙型肝炎数据集,其中许多药物仅在单臂研究中进行了检查。我们展示了将我们的方法应用于该数据集的结果。