Testing in a Prespecified Subgroup and the Intent-to-Treat Population.

Mark D Rothmann, Jenny J Zhang, Laura Lu, Thomas R Fleming
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引用次数: 28

Abstract

In many settings, testing has been proposed to assess the effect of an experimental regimen within a biomarker-positive subgroup where it is biologically plausible that benefit is stronger in such patients, and in the overall population that also includes biomarker-negative subjects less likely to benefit from that regimen. A statistically favorable result in the biomarker-positive subgroup would lead to a claim for that subgroup, whereas a statistically favorable result for the overall population would lead to a claim that includes both biomarker subgroups. The latter setting is problematic when biomarker-negative patients truly do not benefit from the experimental regimen. When it is prespecified that biomarker-negative patients should not be included in the primary analysis of treatment effect in biomarker-positive patients because of the likelihood that treatment effects would differ between the 2 subgroups, it is logically inconsistent to include biomarker-positive patients in the primary analysis of treatment effect in biomarker-negative patients.

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在预先指定的亚组和意向治疗人群中进行测试。
在许多情况下,已经提出了测试来评估实验方案在生物标志物阳性亚组中的效果,在生物学上合理的情况下,这些患者的获益更强,而在包括生物标志物阴性受试者在内的总体人群中,不太可能从该方案中获益。在生物标志物阳性亚组中,统计学上有利的结果将导致对该亚组的权利要求,而在总体上有利的结果将导致包括两个生物标志物亚组的权利要求。当生物标志物阴性的患者确实不能从实验方案中获益时,后一种设置是有问题的。如果预先规定生物标志物阴性患者不应纳入生物标志物阳性患者治疗效果的初步分析,因为两个亚组之间的治疗效果可能不同,那么将生物标志物阳性患者纳入生物标志物阴性患者治疗效果的初步分析在逻辑上是不一致的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Drug Information Journal
Drug Information Journal 医学-卫生保健
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审稿时长
6-12 weeks
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