Infectious Disease Epidemiology Group, Weill Cornell Medical College in Qatar, Cornell University, Qatar Foundation, Education City, Doha, Qatar; Department of Healthcare Policy and Research, Weill Cornell Medical College, Cornell University, NY, USA.
Infectious Disease Epidemiology Group, Weill Cornell Medical College in Qatar, Cornell University, Qatar Foundation, Education City, Doha, Qatar; Department of Healthcare Policy and Research, Weill Cornell Medical College, Cornell University, NY, USA; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, USA.
Comput Biol Med. 2014 Jul;50:1-8. doi: 10.1016/j.compbiomed.2014.03.008. Epub 2014 Apr 13.
In this study, we illustrate the utility of an agent-based simulation to inform a trial design and how this supports outcome interpretation of randomized controlled trials (RCTs). We developed agent-based Monte Carlo models to simulate existing landmark HIV RCTs, such as the Partners in Prevention HSV/HIV Transmission Study. We simulated a variation of this study using valacyclovir therapy as the intervention, and we used a male circumcision RCT based on the Rakai Male Circumcision Trial. Our results indicate that a small fraction (20%) of the simulated Partners in Prevention HSV/HIV Transmission Study realizations rejected the null hypothesis, which was no effect from the intervention. Our results also suggest that an RCT designed to evaluate the effectiveness of a more potent drug regimen for HSV-2 suppression (valacyclovir therapy) is more likely to identify the efficacy of the intervention. For the male circumcision RCT simulation, the greater biological effect of the male circumcision yielded a major fraction (81%) of RCT realizations' that rejects the null hypothesis, which was no effect from the intervention. Our study highlights how agent-based simulations synthesize individual variation in the epidemiological context of the RCT. This methodology will be particularly useful for designing RCTs aimed at evaluating combination prevention interventions in community-based RCTs, wherein an intervention׳s effectiveness is challenging to predict.
在本研究中,我们展示了基于代理的模拟在为试验设计提供信息以及如何支持随机对照试验(RCT)的结果解释方面的效用。我们开发了基于代理的蒙特卡罗模型来模拟现有的艾滋病毒 RCT,例如预防伙伴 HSV/HIV 传播研究。我们使用伐昔洛韦治疗作为干预措施模拟了该研究的一种变体,我们还使用了基于 Rakai 男性包皮环切试验的男性包皮环切 RCT。我们的结果表明,在模拟的预防伙伴 HSV/HIV 传播研究实现中,只有一小部分(20%)拒绝了干预没有效果的零假设。我们的结果还表明,设计用于评估更有效的 HSV-2 抑制药物方案(伐昔洛韦治疗)的 RCT 更有可能确定干预的效果。对于男性包皮环切 RCT 模拟,男性包皮环切的更大生物学效应导致 81%的 RCT 实现拒绝了干预没有效果的零假设。我们的研究强调了基于代理的模拟如何在 RCT 的流行病学背景下综合个体差异。这种方法对于设计旨在评估社区 RCT 中基于组合的预防干预措施的 RCT 将特别有用,因为很难预测干预措施的有效性。