Zee Jarcy, Xie Sharon X
Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA, USA.
Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, PA, USA
Clin Trials. 2015 Aug;12(4):333-41. doi: 10.1177/1740774515583488. Epub 2015 May 14.
In studies with surrogate outcomes available for all subjects and true outcomes available for only a subsample, survival analysis methods are needed that incorporate both endpoints in order to assess treatment effects.
We develop a semiparametric estimated likelihood method for the proportional hazards model with discrete time data and a binary covariate of interest. Our proposed method allows for real-time validation of surrogate outcomes and flexible censoring mechanisms.
Our proposed estimator is consistent and asymptotically normal. Through numerical studies, we showed that our proposed method for estimating a covariate effect is unbiased compared to the naïve estimator that uses only surrogate endpoints and is more efficient with moderate missingness compared to the complete-case estimator that uses only true endpoints. We further demonstrated the advantages of our proposed method in comparison with existing approaches when there is real-time validation. We also illustrated the use of our proposed method by estimating the effect of gender on time to detection of Alzheimer's disease using data from the Alzheimer's Disease Neuroimaging Initiative.
The proposed method is able to account for the uncertainty of surrogate outcomes using a validation subsample of true outcomes in estimating a binary covariate effect. The proposed estimator can outperform standard semiparametric survival analysis methods and can therefore save on costs of a trial or improve power in detecting treatment effects.
在所有受试者均可获得替代结局,而仅部分子样本可获得真实结局的研究中,需要采用将两种结局都纳入的生存分析方法来评估治疗效果。
我们针对具有离散时间数据和感兴趣的二元协变量的比例风险模型开发了一种半参数估计似然方法。我们提出的方法允许对替代结局进行实时验证,并采用灵活的删失机制。
我们提出的估计量是一致的且渐近正态。通过数值研究,我们表明,与仅使用替代终点的朴素估计量相比,我们提出的估计协变量效应的方法是无偏的,并且与仅使用真实终点的完全病例估计量相比,在存在中度缺失时效率更高。当存在实时验证时,我们进一步证明了我们提出的方法与现有方法相比的优势。我们还通过使用来自阿尔茨海默病神经影像倡议的数据估计性别对阿尔茨海默病检测时间的影响,展示了我们提出的方法的应用。
所提出的方法能够在估计二元协变量效应时,使用真实结局的验证子样本考虑替代结局的不确定性。所提出的估计量可以优于标准的半参数生存分析方法,因此可以节省试验成本或提高检测治疗效果的效能。