基于集成机器学习的临床特征排序揭示多形性胶质母细胞瘤的最高生存因素

IF 5.4 Q1 COMPUTER SCIENCE, INFORMATION SYSTEMS Journal of healthcare informatics research Pub Date : 2023-09-20 DOI:10.1007/s41666-023-00138-1
Gabriel Cerono, Ombretta Melaiu, Davide Chicco
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引用次数: 0

摘要

多形性胶质母细胞瘤(GM)是一种中枢神经系统恶性肿瘤,被认为具有高度侵袭性,通常具有可怕的生存预后。因此,准确的预后是决定一个好的治疗方案的关键。在这种情况下,将计算智能应用于诊断患有这种疾病的患者的电子健康记录(EHRs)数据,可用于预测患者的生存时间。在这项研究中,我们评估了不同的机器学习模型来预测胶质母细胞瘤患者的生存时间,并进一步研究了哪些特征最能预测生存时间。我们将我们的计算方法应用于胶质母细胞瘤患者电子病历的三个不同的独立开放数据集:84例患者的Shieh数据集,647例患者的Berendsen数据集和60例患者的Lammer数据集。我们的生存时间预测技术在每个数据集中获得的一致性指数(C-index)在Shieh数据集中为0.583,在Berendsen数据集中为C-index = 0.776,在Lammer数据集中为C-index = 0.64。由于关于本文分析的三个数据集的原始研究并没有提供关于生存时间最具预测性的临床特征的见解,因此我们调查了这些数据集中特征的重要性。为此,我们利用随机生存森林,这是一种基于决策树的算法,能够模拟不同特征之间的非线性相互作用,可能能够更好地捕捉这些患者高度复杂的临床和遗传状态。我们的发现可以影响临床实践,帮助临床医生和患者决定哪种治疗方案最适合他们独特的临床状况。
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Clinical Feature Ranking Based on Ensemble Machine Learning Reveals Top Survival Factors for Glioblastoma Multiforme
Abstract Glioblastoma multiforme (GM) is a malignant tumor of the central nervous system considered to be highly aggressive and often carrying a terrible survival prognosis. An accurate prognosis is therefore pivotal for deciding a good treatment plan for patients. In this context, computational intelligence applied to data of electronic health records (EHRs) of patients diagnosed with this disease can be useful to predict the patients’ survival time. In this study, we evaluated different machine learning models to predict survival time in patients suffering from glioblastoma and further investigated which features were the most predictive for survival time. We applied our computational methods to three different independent open datasets of EHRs of patients with glioblastoma: the Shieh dataset of 84 patients, the Berendsen dataset of 647 patients, and the Lammer dataset of 60 patients. Our survival time prediction techniques obtained concordance index (C-index) = 0.583 in the Shieh dataset, C-index = 0.776 in the Berendsen dataset, and C-index = 0.64 in the Lammer dataset, as best results in each dataset. Since the original studies regarding the three datasets analyzed here did not provide insights about the most predictive clinical features for survival time, we investigated the feature importance among these datasets. To this end, we then utilized Random Survival Forests, which is a decision tree-based algorithm able to model non-linear interaction between different features and might be able to better capture the highly complex clinical and genetic status of these patients. Our discoveries can impact clinical practice, aiding clinicians and patients alike to decide which therapy plan is best suited for their unique clinical status.
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