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初步研究早期终止的图表。

Charts for the early stopping of pilot studies.

作者信息

Mehta C R, Cain K C

出版信息

J Clin Oncol. 1984 Jun;2(6):676-82. doi: 10.1200/JCO.1984.2.6.676.

Abstract

Cooperative oncology groups usually run pilot studies of new agents or combinations concurrently with their major randomized clinical trials. A primary objective of these studies is to determine whether the new regimen should be tested further in a group-wide clinical trial. The accrual goals of such pilot studies are typically fixed in advance at between 30 and 40 patients, on the grounds that this number provides a reasonably tight confidence interval on the true response rate. Nevertheless early termination of pilot studies is often desirable either because the regimen appears inactive or because early results indicate extreme activity and justify immediate testing in a randomized study. Statistical charts are provided for early termination in both these situations. The charts are read by specifying the number of evaluable patients already accrued, the number of responses observed and the minimum true response rate, theta 0, at which the regimen would be considered active. The charts provide the posterior probability that the true response rate exceeds theta 0, that is, that the regimen is active. An additional chart that computes a 90% probability interval for the true response rate, based on the observed rate and sample size, is also provided. The use of the chart is illustrated with two examples from the Eastern Cooperative Oncology Group.

摘要

肿瘤协作组通常在开展主要随机临床试验的同时,对新药物或联合用药方案进行试点研究。这些研究的一个主要目的是确定新方案是否应在全组范围内的临床试验中进一步测试。此类试点研究的入组目标通常预先设定为30至40名患者,理由是这个数量能在真实缓解率上提供一个相当紧凑的置信区间。然而,试点研究往往需要提前终止,这要么是因为该方案似乎无效,要么是因为早期结果显示活性极高,从而有理由立即在随机研究中进行测试。本文提供了在这两种情况下提前终止试验的统计图表。通过指定已入组的可评估患者数量、观察到的缓解数量以及该方案被视为有效的最小真实缓解率θ0来读取这些图表。这些图表提供了真实缓解率超过θ0的后验概率,即该方案有效的概率。还提供了一个额外的图表,该图表基于观察到的缓解率和样本量计算真实缓解率的90%概率区间。本文用东部肿瘤协作组的两个例子说明了图表的使用方法。

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