There is an increasing number of potential biomarkers that could allow for early assessment of treatment response or disease progression. However, measurements of quantitative biomarkers are subject to random variability. Hence, differences of a biomarker in longitudinal measurements do not necessarily represent real change but might be caused by this random measurement variability. Before utilizing a quantitative biomarker in longitudinal studies, it is therefore essential to assess the measurement repeatability. Measurement repeatability obtained from test-retest studies can be quantified by the repeatability coefficient (RC), which is then used in the subsequent longitudinal study to determine if a measured difference represents real change or is within the range of expected random measurement variability. The quality of the point estimate of RC therefore directly governs the assessment quality of the longitudinal study. RC estimation accuracy depends on the case number in the test-retest study, but despite its pivotal role, no comprehensive framework for sample size calculation of test-retest studies exists. To address this issue, we have established such a framework, which allows for flexible sample size calculation of test-retest studies, based upon newly introduced criteria concerning assessment quality in the longitudinal study. This also permits retrospective assessment of prior test-retest studies.
翻译:因此,纵向测量的生物标志的差别不一定代表实际变化,而可能是这种随机测量变化造成的。因此,在利用纵向研究的定量生物标志之前,评估可重复性至关重要。从测试-再测试研究中获得的测量重复性可以用重复性系数(RC)进行量化,该系数随后在随后的纵向研究中使用,以确定测量的差别是否代表实际变化或是否在预期随机测量变化的范围内。因此,纵向测量的生物标志的差别不一定代表实际变化,而是这种随机测量变化造成的。在使用定量生物标志之前,必须评估纵向研究的可重复性。因此,在使用定量生物标志之前,必须先行评估试验-再测试研究的样本大小计算没有综合框架。为了解决这一问题,我们建立了这样一个框架,以便根据最近采用的关于纵向研究评估质量的标准,灵活地抽样计算测试-再测试研究的规模。这也允许对以前试验-再测试研究进行追溯性评估。