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临床试验变得越来越复杂:对超过 16000 项试验数据的机器学习分析。

Clinical trials are becoming more complex: a machine learning analysis of data from over 16,000 trials.

机构信息

Boston Consulting Group, 80 Charlotte Street, London, W1T 4DF, UK.

Boston Consulting Group, 75 Avenue de la Grande Armée, 75016, Paris, France.

出版信息

Sci Rep. 2024 Feb 12;14(1):3514. doi: 10.1038/s41598-024-53211-z.

Abstract

The past decade has seen substantial innovation in clinical trials, including new trial formats, endpoints, and others. Also there have been regulatory changes, increasing competitive pressures and other external factors which impact clinical trials. In parallel, trial timelines have increased and success rates remain stubbornly low. This has led many observers to question whether clinical trials have become overly complex and if this complexity is always needed. Here we present a large-scale analysis of protocols and other data from over 16,000 trials. Using a machine learning algorithm, we automatically assessed key features of these trials, such as number of endpoints, number of inclusion-exclusion criteria and others. Using a regression analysis we combined these features into a new metric, the Trial Complexity Score, which correlates with overall clinical trial duration. Looking at this score across different clinical phases and therapeutic areas we see substantial increases over time, suggesting that clinical trials are indeed becoming more complex. We discuss drivers of increasing trial complexity, necessary or helpful ('good') complexity versus unnecessary ('bad') complexity, and we explore mechanisms of how sponsors of clinical trials can reduce trial complexity where appropriate.

摘要

在过去的十年中,临床试验领域出现了大量的创新,包括新的试验设计、终点等。此外,监管法规也发生了变化,竞争压力不断增加以及其他外部因素也对临床试验产生了影响。与此同时,试验时间延长了,但成功率仍然很低。这使得许多观察家质疑临床试验是否变得过于复杂,以及这种复杂性是否总是必要的。在这里,我们对来自 16000 多项试验的方案和其他数据进行了大规模分析。我们使用机器学习算法自动评估了这些试验的关键特征,例如终点数量、纳入排除标准数量等。我们使用回归分析将这些特征组合成一个新的指标,即试验复杂度评分,它与临床试验的总持续时间相关。我们观察不同临床阶段和治疗领域的这个评分,发现随着时间的推移,它有了显著的增加,这表明临床试验确实变得更加复杂了。我们讨论了导致试验复杂性增加的因素,必要或有益的(“好”)复杂性与不必要的(“坏”)复杂性,并探讨了临床试验发起者在适当的情况下如何降低试验复杂性的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa6f/10861486/7c5f420b6321/41598_2024_53211_Fig1_HTML.jpg

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