Follmann Dean, Fay Michael, Magaret Craig, Gilbert Peter
medRxiv. 2021 Sep 2:2021.08.31.21262908. doi: 10.1101/2021.08.31.21262908.
SARS-CoV-2 continues to evolve and the vaccine efficacy against variants is challenging to estimate. It is now common in phase III vaccine trials to provide vaccine to those randomized to placebo once efficacy has been demonstrated, precluding a direct assessment of placebo controlled vaccine efficacy after placebo vaccination. In this work we extend methods developed for estimating vaccine efficacy post placebo vaccination to allow variant specific time varying vaccine efficacy, where time is measured since vaccination. The key idea is to infer counterfactual strain specific placebo case counts by using surveillance data that provide the proportions of the different strains. This blending of clinical trial and observational data allows estimation of strain-specific time varying vaccine efficacy, or sieve effects, including for strains that emergent after placebo vaccination. The key requirements are that surveillance strain distribution accurately reflect the strain distribution for a placebo group, throughout follow-up after placebo group vaccination and that at least one strain is present before and after placebo vaccination. For illustration, we develop a Poisson approach for an idealized design under a rare disease assumption and then use a proportional hazards modeling to better reflect the complexities of field trials with staggered entry, crossover, and smoothly varying strain specific vaccine efficacy We evaluate these by theoretical work and simulations, and demonstrate that useful estimation of the efficacy profile is possible for strains that emerge after vaccination of the placebo group. An important principle is to incorporate sensitivity analyses to guard against mis-specfication of the strain distribution. We also provide an approach for use when genotyping of the infecting strains of the trial participants has not been done.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)持续进化,针对变异株的疫苗效力难以估计。在III期疫苗试验中,一旦证明了效力,就会向随机分配到安慰剂组的受试者提供疫苗,这使得无法直接评估安慰剂接种后的安慰剂对照疫苗效力。在这项研究中,我们扩展了用于估计安慰剂接种后疫苗效力的方法,以允许针对变异株的随时间变化的疫苗效力,这里的时间是自接种以来的测量值。关键思想是通过使用提供不同毒株比例的监测数据来推断反事实毒株特异性安慰剂病例数。这种临床试验数据与观察数据的融合使得能够估计毒株特异性随时间变化的疫苗效力,即筛选效应,包括对安慰剂接种后出现的毒株。关键要求是监测毒株分布在安慰剂组接种后的整个随访期间准确反映安慰剂组的毒株分布,并且在安慰剂接种前后至少有一种毒株存在。为了说明这一点,我们在罕见病假设下为理想化设计开发了一种泊松方法,然后使用比例风险模型来更好地反映具有交错入组、交叉和毒株特异性疫苗效力平滑变化的现场试验的复杂性。我们通过理论研究和模拟对这些方法进行了评估,并证明对于安慰剂组接种后出现的毒株,可以对效力概况进行有用的估计。一个重要原则是纳入敏感性分析以防止毒株分布的错误设定。我们还提供了一种在未对试验参与者的感染毒株进行基因分型时使用的方法。