CDER/OTS/OB/DBV, and CDER/OND/OHOP/DOP-1, U.S. Food and Drug Administration, Silver Spring, MD 20993, USA.
Clin Cancer Res. 2012 Sep 15;18(18):4872-6. doi: 10.1158/1078-0432.CCR-11-3118. Epub 2012 Jul 2.
Group sequential designs (GSD), which provide for interim monitoring of efficacy data and allow potential early trial termination while preserving the type I error rate, have become commonplace in oncology clinical trials. Although ethically appealing, GSDs tend to overestimate the true treatment effect size at early interim analyses. Overestimation of the treatment effect may exaggerate the benefit of a drug and provide imprecise information for physicians and their patients about a drug's true effect. The cause and effect of such a phenomenon are generally not well understood by many in clinical trial practice. In this article, we provide a graphical explanation for why the phenomenon of overestimation in GSDs occurs. The potential overestimation of the magnitude of the treatment effect is of particular concern in oncology, in which the more subjective endpoint of progression-free survival has increasingly been adopted as the primary endpoint in pivotal phase III trials.
分组序贯设计(GSD)在肿瘤临床试验中已变得非常普遍,它提供了对疗效数据的中期监测,并允许潜在的早期试验终止,同时保持了Ⅰ类错误率。虽然从伦理角度来看很有吸引力,但 GSD 在早期中期分析中往往会高估真实的治疗效果大小。治疗效果的高估可能夸大药物的益处,并为医生及其患者提供关于药物真实效果的不精确信息。这种现象的因果关系通常不为许多临床试验实践中的人所理解。在本文中,我们提供了一个图形解释,说明为什么 GSD 中会出现高估现象。在肿瘤学中,这种治疗效果的高估幅度的潜在性特别令人关注,因为无进展生存期这一更主观的终点越来越多地被用作关键性 III 期试验的主要终点。