...
首页> 外文期刊>Contemporary clinical trials >A new adaptive design based on Simon's two-stage optimal design for phase II clinical trials
【24h】

A new adaptive design based on Simon's two-stage optimal design for phase II clinical trials

机译:基于Simon两阶段最佳设计的II期临床试验新的自适应设计

获取原文
获取原文并翻译 | 示例
           

摘要

Phase II clinical trials are conducted to determine whether a new agent or drug regimen has sufficient promise in treating cancer to merit further testing in larger groups of patients. Both ethical and practical considerations often require early termination of phase II trials if early results clearly indicate that the new regimen is not active or worthy of further investigation. Simon's two-stage designs (1989) are common methods for conducting phase II studies investigating new cancer therapies. Banerjee and Tsiatis (2006) proposed an adaptive two-stage design which allows the sample size at the second stage to depend on the results at the first stage. Their design is more flexible than Simon's, but it is somewhat counter-intuitive: as the response in the first stage increases, the second-stage sample size increases till a certain point and then abruptly becomes zero. In this paper, based on Simon's two-stage optimal design, we propose a new adaptive one which depends on the first stage results using the restrict conditions the conditional type I error and the conditional power. Comparisons are made between Banerjee and Tsiatis' results and our new adaptive designs.
机译:进行II期临床试验以确定新药或新药方案是否具有足够的前景来治疗癌症,值得在大批患者中进行进一步测试。如果早期结果清楚地表明新的治疗方案不活跃或值得进一步研究,那么从伦理和实践角度考虑,通常都要求早期终止II期试验。西蒙(Simon)的两阶段设计(1989)是进行II期研究以研究新的癌症疗法的常用方法。 Banerjee和Tsiatis(2006)提出了一种自适应的两阶段设计,该设计允许第二阶段的样本大小取决于第一阶段的结果。他们的设计比Simon的设计更灵活,但是有点违反直觉:随着第一阶段响应的增加,第二阶段样本的大小会增加到一定点,然后突然变为零。在本文中,基于西蒙的两阶段优化设计,我们提出了一种新的自适应方法,该方法使用限制条件,条件类型I误差和条件功效来取决于第一阶段的结果。 Banerjee和Tsiatis的结果与我们的新自适应设计进行了比较。

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