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Phase II cancer clinical trials with a one-sample log-rank test and its corrections based on the Edgeworth expansion.

机译:具有一样本对数秩检验的II期癌症临床试验及其基于Edgeworth扩展的更正。

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The response rate has been frequently used as the primary endpoint of phase II cancer clinical trials. It may not be an appropriate endpoint when a new treatment is not expected to produce any tumour shrinkage. When a large database for a historical control is available, the direct comparison of survival curves between a new treatment and the historical control may be made in phase II cancer clinical trials. In this paper, a one-sample log-rank test is introduced for the design and analysis of phase II cancer clinical trials with time-to-event endpoints. Corrections to the one-sample log-rank test are also derived based on the Edgeworth expansion. Simulations showed that the original one-sample log-rank test may be preferred if strictly controlling for type I error is important or when the sample size of a phase II trial is as large as 50, and a corrected one-sample log-rank test is used if the sample size of a phase II trial is small. A data set from a clinical trial conducted by the NCIC Clinical Trials Group is used to illustrate the proposed procedures.
机译:缓解率经常被用作II期癌症临床试验的主要终点。当新疗法预期不会产生任何肿瘤缩小时,这可能不是合适的终点。当有大量用于历史对照的数据库可用时,可以在II期癌症临床试验中对新疗法与历史对照之间的生存曲线进行直接比较。本文介绍了一种单样本对数秩检验,用于设计和分析具有事件发生时间终点的II期癌症临床试验。还基于Edgeworth扩展对单样本对数秩检验进行了校正。模拟显示,如果严格控制I型错误很重要或II期试验的样本量最大为50个,并且校正后的一样本对数秩检验,则最好使用原始的一样本对数秩检验。如果II期试验的样本量较小,则使用。 NCIC临床试验小组进行的一项临床试验数据集用于说明所建议的程序。

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