II期临床试验设计:来自东部肿瘤协作组泌尿生殖委员会的转化研究方法

Phase II clinical trial design: methods in translational research from the Genitourinary Committee at the Eastern Cooperative Oncology Group.

作者信息

Gray Robert, Manola Judith, Saxman Scott, Wright John, Dutcher Jan, Atkins Michael, Carducci Michael, See William, Sweeney Christopher, Liu Glenn, Stein Mark, Dreicer Robert, Wilding George, DiPaola Robert S

机构信息

Eastern Cooperative Oncology Group, Harvard School of Public Health, Boston, Massachusetts, USA.

出版信息

Clin Cancer Res. 2006 Apr 1;12(7 Pt 1):1966-9. doi: 10.1158/1078-0432.CCR-05-1136.

Abstract

Given the increase in novel agents and difficulty with planning and completing many phase III studies, various phase II trial design options should be considered to more effectively guide phase III trial plans. The need for novel phase II trial designs has increased, given the number of novel molecular targeted therapies now available for testing, an abundance of cytostatic agents, and limited resources to conduct phase III studies for all interesting agents or combinations. This review will focus on options for phase II trial designs. We review randomized phase II designs with placebo control, randomized selection designs, and randomized discontinuation designs. As agents become available for testing in the clinic, the strengths and weaknesses of different phase II trial designs should be considered to optimize a trial development plan that guides phase III trial decisions more effectively.

摘要

鉴于新型药物的增加以及规划和完成许多III期研究的困难,应考虑各种II期试验设计选项,以便更有效地指导III期试验计划。鉴于目前有大量新型分子靶向疗法可供测试、有大量细胞抑制剂,且用于对所有感兴趣的药物或联合用药进行III期研究的资源有限,对新型II期试验设计的需求增加了。本综述将聚焦于II期试验设计的选项。我们将回顾采用安慰剂对照的随机II期设计、随机选择设计和随机停药设计。随着药物可用于临床测试,应考虑不同II期试验设计的优缺点,以优化试验开发计划,从而更有效地指导III期试验决策。

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