Zhang Min
Department of Biostatistics, University of Michigan, Ann Arbor, MI, 48109-2029, USA,
Lifetime Data Anal. 2015 Jan;21(1):119-37. doi: 10.1007/s10985-014-9291-y. Epub 2014 Feb 13.
In randomized clinical trials, improving efficiency and reducing bias due to chance imbalance in covariates among groups are always of considerable interest. The two purposes are often achieved by some type of covariate adjustment. In trials involving time-to-an-event, Kaplan-Meier and Nelson-Aalen estimators are the most popular nonparametric estimation of survival curves. However, these methods do not permit direct covariate adjustment, missing the important chance of improving efficiency and reducing bias. In this article, we propose robust, covariate adjusted analogues of the Nelson-Aalen and Kaplan-Meier estimators. The method is robust in that it does not require any additional modeling assumptions and hence the resulting estimators are again nonparametric. The robustness is achieved by taking advantage of the study design, i.e., treatments are randomized. Large-sample properties of the proposed estimators are developed, which show that the improvement in efficiency is guaranteed asymptotically. Simulation studies using reasonably small sample sizes further demonstrate the efficiency gain and the ability to reduce or remove bias resulted from chance imbalance to a large degree, e.g., more than 10-fold reduction in bias is achieved. Efficiency improvement and bias reduction are also illustrated by application to a cancer clinical trial. The proposed methods may help to resolve the tension between the need to make best use of data and the unwillingness to make additional assumptions in analyzing data from clinical trials.
在随机临床试验中,提高效率以及减少因各组协变量的随机不平衡而产生的偏差一直备受关注。这两个目的通常通过某种类型的协变量调整来实现。在涉及事件发生时间的试验中,Kaplan-Meier和Nelson-Aalen估计量是生存曲线最常用的非参数估计方法。然而,这些方法不允许直接进行协变量调整,从而错失了提高效率和减少偏差的重要机会。在本文中,我们提出了Nelson-Aalen和Kaplan-Meier估计量的稳健的、经协变量调整的类似方法。该方法的稳健性在于它不需要任何额外的建模假设,因此所得的估计量再次是非参数的。稳健性是通过利用研究设计实现的,即治疗是随机分配的。我们推导了所提出估计量的大样本性质,结果表明效率的提高在渐近意义上是有保证的。使用合理小样本量的模拟研究进一步证明了效率的提高以及在很大程度上减少或消除因随机不平衡导致的偏差的能力,例如偏差减少超过10倍。通过应用于一项癌症临床试验也说明了效率的提高和偏差的减少。所提出的方法可能有助于解决在充分利用数据的需求与在分析临床试验数据时不愿做出额外假设之间的矛盾。