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首页> 外文期刊>Biometrics: Journal of the Biometric Society : An International Society Devoted to the Mathematical and Statistical Aspects of Biology >Optimal estimator for the survival distribution and related quantities for treatment policies in two-stage randomization designs in clinical trials.
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Optimal estimator for the survival distribution and related quantities for treatment policies in two-stage randomization designs in clinical trials.

机译:在临床试验的两阶段随机设计中,用于生存策略的最佳估计量和治疗策略的相关量。

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摘要

Summary. Two-stage designs, where patients are initially randomized to an induction therapy and then depending upon their response and consent, are randomized to a maintenance therapy, are common in cancer and other clinical trials. The goal is to compare different combinations of primary and maintenance therapies to find the combination that is most beneficial. In practice, the analysis is usually conducted in two separate stages which does not directly address the major objective of finding the best combination. Recently Lunceford, Davidian, and Tsiatis (2002, Biometrics58, 48-57) introduced ad hoc estimators for the survival distribution and mean restricted survival time under different treatment policies. These estimators are consistent but not efficient, and do not include information from auxiliary covariates. In this article we derive estimators that are easy to compute and are more efficient than previous estimators. We also show how to improve efficiency further by taking into account additional information from auxiliary variables. Large sample properties of these estimators are derived and comparisons with other estimators are made using simulation. We apply our estimators to a leukemia clinical trial data set that motivated this study.
机译:概要。在癌症和其他临床试验中很常见的两阶段设计是,患者最初被随机分配到诱导疗法,然后根据他们的反应和同意,被随机分配到维持疗法。目的是比较主要疗法和维持疗法的不同组合,以找到最有益的组合。在实践中,分析通常在两个单独的阶段中进行,这两个阶段不会直接解决寻找最佳组合的主要目标。最近,Lunceford,Davidian和Tsiatis(2002,Biometrics58,48-57)引入了针对不同治疗策略的生存分布和平均受限生存时间的临时估计量。这些估计量是一致的,但效率不高,并且不包括辅助协变量的信息。在本文中,我们得出的估算器比以前的估算器更易于计算且效率更高。我们还将展示如何通过考虑来自辅助变量的其他信息来进一步提高效率。推导了这些估计量的大样本属性,并使用模拟与其他估计量进行了比较。我们将估算值应用于激发这项研究的白血病临床试验数据集。

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