首页> 外文期刊>Statistics in medicine >Testing of evaluation bias for progression free survival endpoint in oncology clinical trials
【24h】

Testing of evaluation bias for progression free survival endpoint in oncology clinical trials

机译:肿瘤临床试验中无进展生存终点评估偏倚的检验

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Progression-free survival is an increasingly popular end point in oncology clinical trials. A complete blinded independent central review (BICR) is often required by regulators in an attempt to reduce the bias in progression-free survival (PFS) assessment. In this paper, we propose a new methodology that uses a sample-based BICR as an audit tool to decide whether a complete BICR is needed. More specifically, we propose a new index, the differential risk, to measure the reading discordance pattern, and develop a corresponding hypothesis testing procedure to decide whether the bias in local evaluation is acceptable. Simulation results demonstrate that our new index is sensitive to the change of discordance pattern; type I error is well controlled in the hypothesis testing procedure, and the calculated sample size provides the desired power. Copyright (C) 2016 John Wiley & Sons, Ltd.
机译:无进展生存期是肿瘤临床试验中越来越受欢迎的终点。监管机构通常要求进行完整的独立盲文中央评估(BICR),以减少无进展生存期(PFS)评估的偏差。在本文中,我们提出了一种新的方法,该方法使用基于样本的BICR作为审核工具来决定是否需要完整的BICR。更具体地说,我们提出了一个新的指标,即差异风险,以衡量阅读不一致的情况,并制定相应的假设检验程序,以决定本地评估中的偏差是否可以接受。仿真结果表明,我们的新指标对不一致模式的变化敏感。在假设检验程序中,I型错误得到了很好的控制,并且计算出的样本量提供了所需的功效。版权所有(C)2016 John Wiley&Sons,Ltd.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号