Survival Stacking Ensemble Model for Lung Cancer Risk Prediction.

Eduardo Alonso, Xabier Calle, Ibai Gurrutxaga, Andoni Beristain
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Abstract

The most well-established risk factor for lung cancer (LC) is smoking, responsible for approximately 85% of cases. The Lung Cancer Risk Assessment Tool (LCRAT) is a key advancement in this field, which predicts individual risk based on factors like smoking habits, demographic details, personal and family medical history, and environmental exposures. This paper proposes a model with fewer features that improves state of the art performance, using a simplified stacking ensemble, making it more accessible and easier to implement in routine healthcare practice. The data used in this work were derived from two cohorts in the United States: The National Lung Screening Trial (NLST) and the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial. Both our model and LCRAT achieve an AUC of 0.799 and 0.782 on test respectively. In terms of percentage of positives, in the 50% of the population, both detect 0.766 and 0.754 of the cases. The ensemble of different survival models enhances robustness by mitigating the weakness of individual models and directly impacts the efficiency of the model, increasing the efficiency and generalizability.

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用于肺癌风险预测的生存期叠加集合模型
肺癌(LC)最常见的风险因素是吸烟,约 85% 的病例都与吸烟有关。肺癌风险评估工具(LCRAT)是该领域的一项重要进展,它可根据吸烟习惯、人口统计学细节、个人和家族病史以及环境暴露等因素预测个人风险。本文提出了一种功能较少的模型,它采用简化的堆叠组合,提高了技术性能,使其更易于在常规医疗实践中使用。这项工作中使用的数据来自美国的两个队列:美国国家肺癌筛查试验(NLST)和前列腺癌、肺癌、结直肠癌和卵巢癌筛查试验(PLCO)。我们的模型和 LCRAT 在测试中的 AUC 分别为 0.799 和 0.782。就阳性比例而言,在 50%的人群中,两者分别检测出 0.766 和 0.754 个病例。不同生存模型的集合通过减轻单个模型的弱点而增强了稳健性,并直接影响到模型的效率,提高了效率和普适性。
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