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早期肿瘤学试验:为何有如此多的设计?

Early-Phase Oncology Trials: Why So Many Designs?

机构信息

Laboratory of Analysis, Geometry and Applications, laboratoire d'excellence Inflamex, University of Sorbonne Paris North, Villetaneuse, France.

出版信息

J Clin Oncol. 2022 Oct 20;40(30):3529-3536. doi: 10.1200/JCO.21.02493. Epub 2022 Aug 12.

Abstract

The past 30 years have seen a considerable effort on the part of statisticians to improve the design and accuracy of early-phase oncology trials. Some of this effort has been rewarded via successful implementation in actual trials, yet it would be fair to say that among clinicians, there remains some reluctance to fully embrace more efficient model-based approaches. One reason for such reticence is the difficulty in understanding exactly what is being offered by more modern designs. Although it is generally accepted that these designs offer improvements over the old standard 3 + 3 design, a new question has then to be addressed: How should we decide among the new proposals which one is the best for our purpose? In this study, we recall 15 designs that are currently proposed and in use. We show that among these 15 designs, many are operationally identical. These 15 designs reduce to three broad classes of designs. This review helps summarize their properties and differences and highlights that certain designs require ad hoc modifications to ensure satisfactory performance.

摘要

在过去的 30 年中,统计学家们做出了相当大的努力来改进肿瘤早期阶段试验的设计和准确性。其中一些努力已经在实际试验中得到了成功实施,但公平地说,在临床医生中,仍然存在一些不愿意完全接受更有效的基于模型的方法的情况。这种犹豫的一个原因是难以确切理解更现代的设计所提供的内容。尽管人们普遍认为这些设计相对于旧的标准 3 + 3 设计有所改进,但随后又出现了一个新问题:我们应该如何在新提案中做出选择,哪种设计最适合我们的目的?在这项研究中,我们回顾了目前提出并正在使用的 15 种设计。我们表明,在这 15 种设计中,许多在操作上是相同的。这 15 种设计可以归结为三大类设计。本综述有助于总结它们的特性和差异,并强调某些设计需要特别修改以确保满意的性能。

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