Improving precision of vaccine efficacy evaluation using immune correlate data in time-to-event models.

IF 6.9 1区 医学 Q1 IMMUNOLOGY
Julie Dudášová, Zdeněk Valenta, Jeffrey R Sachs
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引用次数: 0

Abstract

Understanding potential differences in vaccine-induced protection between demographic subgroups is key for vaccine development. Vaccine efficacy evaluation across these subgroups in phase 2b or 3 clinical trials presents challenges due to lack of precision: such trials are typically designed to demonstrate overall efficacy rather than to differentiate its value between subgroups. This study proposes a method for estimating vaccine efficacy using immunogenicity (instead of vaccination status) as a predictor in time-to-event models. The method is applied to two datasets from immunogenicity sub-studies of vaccine phase 3 clinical trials for zoster and dengue vaccines. Results show that using immunogenicity-based estimation of efficacy in subgroups using time-to-event models is more precise than the standard estimation. Incorporating immune correlate data in time-to-event models improves precision in estimating efficacy (i.e., yields narrower confidence intervals), which can assist vaccine developers and public health authorities in making informed decisions.

利用时间到事件模型中的免疫相关数据提高疫苗疗效评估的精确度。
了解不同人口亚群在疫苗诱导保护方面的潜在差异是疫苗开发的关键。由于缺乏精确性,在 2b 或 3 期临床试验中对这些亚群进行疫苗疗效评估面临挑战:此类试验通常旨在证明总体疗效,而不是区分亚群之间的价值。本研究提出了一种在时间到事件模型中使用免疫原性(而非疫苗接种状态)作为预测因子来估算疫苗疗效的方法。该方法应用于带状疱疹疫苗和登革热疫苗 3 期临床试验免疫原性子研究的两个数据集。结果表明,使用基于免疫原性的时间到事件模型估算亚组疗效比标准估算更为精确。将免疫相关数据纳入时间到事件模型可提高疗效估计的精确度(即产生更窄的置信区间),这有助于疫苗开发人员和公共卫生机构做出明智的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
NPJ Vaccines
NPJ Vaccines Immunology and Microbiology-Immunology
CiteScore
11.90
自引率
4.30%
发文量
146
审稿时长
11 weeks
期刊介绍: Online-only and open access, npj Vaccines is dedicated to highlighting the most important scientific advances in vaccine research and development.
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