Futility Interim Analyses - A Plea for Simplicity.

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Gian-Andrea Thanei, Gaëlle Klingelschmitt, Claude Berge, Hans Ulrich Burger
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引用次数: 0

Abstract

Futility interim analyses remain a topic of anxiety for most clinical drug development teams. While they can significantly reduce the risk involved in the development of innovative therapies and do so at a minimal cost, they are not used frequently enough. Development teams often shy away due to the fear of terminating a potentially successful therapy by mistake. We believe these risks are overestimated and hence necessitate a simple and effective communication to be better understood. The planning of futilities often evolves into complex statistical modeling exercises where various scenarios are simulated and multiple risk metrics are calculated. To assist teams in such discussions we propose a straightforward strategy for establishing a range for the futility threshold and an intuitive futility risk measure to evaluate the associated risks.

无用的中期分析——请求简单。
对于大多数临床药物开发团队来说,无效的中期分析仍然是一个令人焦虑的话题。虽然它们可以显著降低开发创新疗法所涉及的风险,并以最低的成本做到这一点,但它们的使用不够频繁。由于害怕错误地终止潜在的成功疗法,开发团队通常会回避。我们认为这些风险被高估了,因此有必要进行简单有效的沟通,以便更好地理解。公用事业的规划通常演变为复杂的统计建模练习,其中模拟各种场景并计算多个风险度量。为了帮助团队进行这样的讨论,我们提出了一个直接的策略来建立一个无效阈值的范围,以及一个直观的无效风险度量来评估相关的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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