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Automatically Labeling $200B Life-Saving Datasets: A Large Clinical Trial Outcome Benchmark

A large clinical trial outcome dataset, CTO, compiled from various weakly supervised sources, achieves high accuracy in predicting outcomes, making it valuable for optimizing therapeutic programs.

Year
2024
Venue
arXiv 2024
Authors
5
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arxiv.org/abs/2406.10292v2ARXIV-DEFAULT
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Abstract

Background: The global cost of drug discovery and development exceeds $200 billion annually, with clinical trial outcomes playing a critical role in the regulatory approval of new drugs and impacting patient outcomes. Despite their significance, large-scale, high-quality clinical trial outcome data are not readily available to the public, limiting advances in trial outcome predictive modeling. Methods: We introduce the Clinical Trial Outcome (CTO) knowledge base, a fully reproducible, large-scale (around 125K drug and biologics trials), open-source of clinical trial information including large language model (LLM) interpretations of publications, matched trials over phases, sentiment analysis from news, stock prices of trial sponsors, and other trial-related metrics. From this knowledge base, we additionally performed manual annotation of a set of recent clinical trials from 2020-2024. Results: We evaluated the quality of our knowledge base by generating high-quality trial outcome labels that demonstrate strong agreement with previously published expert annotations, achieving an F1 score of 94 for Phase 3 trials and 91 across all phases. Additionally, we benchmarked a suite of standard machine learning models on our manually annotated set, highlighting the distribution shift of recent trials and the need for continuously updated labeling methods. Conclusions: By analyzing CTO's performance on recent trials, we showed a need for recent, high-quality trial outcome labels. We release our knowledge base and labels to the public at https://chufangao.github.io/CTOD, which will also be regularly updated to support ongoing research in clinical trial outcomes, offering insights that could optimize the drug development process.

Authors

5