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Machine Learning-Based Modeling of Big Clinical Trials Data for Adverse Outcome Prediction: A Case Study of Death Events

机译:基于机器学习的不良结果预测的大型临床试验数据建模:死亡事件的案例研究

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It is known that clinical trials have potential risks for participants, which could result in unexpected adverse events. To quantify and predict the risk of adverse outcomes, we leverage a large amount of clinical reports to build machine learning models to predict adverse outcomes. We focused on death events as the predicting target in this study. From Clinicaltrial.gov, we collected 28,340 reports and transformed the data into vectorized machine learning features. These features were harmonized across studies using semantic mapping and feature selection techniques. The resulting selected clinical trial features were used to build five machine learning models for prediction. We evaluated and compared relative model performances for the prediction task. Results show that the logistic regression algorithm achieved the best overall receiver operating characteristic score at 0.7344. This exploratory study showed that it is feasible to use clinical trial factors to predict adverse outcomes. We demonstrated the approach by focusing on building machine learning models to predict death outcomes. Predicting adverse outcomes could help clinical trials estimate harmful risks and design better mechanisms to protect participants. We hope by using our models, a clinical trial expert will be able to assess whether serious adverse events are likely to occur in a clinical trial at the early stage and to estimate what potential trial factors could contribute to the potential serious adverse events.
机译:众所周知,临床试验对参与者有潜在的风险,这可能会导致意外的不良事件。为了量化和预测不良结果的风险,我们利用大量的临床报告来构建机器学习模型来预测不良结果。在本研究中,我们将死亡事件作为预测目标。我们从Clinicaltrial.gov收集了28,340个报告,并将数据转换为矢量化的机器学习功能。这些特征在使用语义映射和特征选择技术的研究中得到了统一。由此产生的选定的临床试验特征被用于构建五个机器学习模型以进行预测。我们评估并比较了预测任务的相对模型性能。结果表明,逻辑回归算法在0.7344处获得了最佳的总体接收器工作特性评分。这项探索性研究表明,使用临床试验因素预测不良结局是可行的。我们通过专注于构建机器学习模型来预测死亡结果来演示了该方法。预测不良结果可能有助于临床试验评估有害风险并设计更好的机制来保护参与者。我们希望通过使用我们的模型,临床试验专家将能够评估早期临床试验中是否可能发生严重不良事件,并估计哪些潜在的试验因素可能导致潜在的严重不良事件。

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