Arnold Kellyn, Antunes Luis, Coles Briana, Lee Hopin
IQVIA, Methods and Evidence Generation, London, United Kingdom.
IQVIA, Methods and Evidence Generation, Lisbon, Portugal.
Front Drug Saf Regul. 2024 Apr 11;4:1380568. doi: 10.3389/fdsfr.2024.1380568. eCollection 2024.
External comparator (EC) studies are increasingly being used to generate evidence that supports the evaluation of emerging pharmacological treatments for regulatory and health technology assessment (HTA) purposes. However, the reliability of evidence generated from EC studies can vary. In this paper, we outline how an existing framework for causal inference, the target trial emulation (TTE) framework, can be appropriately applied to improve the design and analysis of EC studies. Applying the TTE framework involves specifying the protocol of an ideal target trial which would answer the causal question of interest, then emulating its key elements under real-world (RW) settings. We describe each component of the original TTE framework and explain how it can be applied to EC studies, supplemented with practical recommendations. We also highlight special considerations and limitations in applying the TTE framework to EC studies. We describe how the TTE framework can be applied to improve the clarity, transparency, and reliability of evidence generated from EC studies.
外部对照(EC)研究越来越多地被用于生成证据,以支持对新兴药物治疗进行监管和卫生技术评估(HTA)。然而,EC研究产生的证据的可靠性可能各不相同。在本文中,我们概述了如何适当地应用现有的因果推断框架——目标试验模拟(TTE)框架,以改进EC研究的设计和分析。应用TTE框架需要指定一个理想目标试验的方案,该方案将回答感兴趣的因果问题,然后在现实世界(RW)环境中模拟其关键要素。我们描述了原始TTE框架的每个组成部分,并解释了如何将其应用于EC研究,并辅以实际建议。我们还强调了将TTE框架应用于EC研究时的特殊考虑因素和局限性。我们描述了TTE框架如何应用于提高EC研究产生的证据的清晰度、透明度和可靠性。