RCoxNet: deep learning framework for enhanced cancer survival prediction integrating random walk with restart with mutation and clinical data

Stuti Kumari, Sakshi Gujral, Smruti Panda, Prashant Gupta, Gaurav Ahuja, Debarka Sengupta
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Abstract

Cancer poses a significant global health challenge, characterized by a complex disease progression and disrupted growth regulation. A thorough understanding of cellular and molecular biological mechanisms is essential for developing novel treatments and improving the accuracy of patient survival predictions. While prior studies have leveraged gene expression and clinical data to forecast survival outcomes through current machine learning and deep learning approaches, gene mutation data despite being a widely recognized metric has rarely been incorporated due to its limited information, inadequate representation of gene relationships, and data sparsity, which negatively affects the robustness, effectiveness, and interpretability of current survival analysis approaches. To overcome the challenges of mutation data sparsity, we propose RCoxNet, a novel deep learning neural network framework that integrates the Random Walk with Restart (RWR) algorithm with a deep learning Cox Proportional Hazards model. By applying this framework to mutation data from cBioportal, our model achieved an average concordance index of 0.62+-0.05 across four cancer types, outperforming existing deep neural network models. Additionally, we identified clinical features critical for differentiating between predicted high- and low-risk patients, with the relevance of these features being partially supported by previous studies.
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RCoxNet:用于增强癌症生存预测的深度学习框架,将随机漫步与突变和临床数据重新开始整合在一起
癌症对全球健康构成重大挑战,其特点是疾病进展复杂,生长调节紊乱。透彻了解细胞和分子生物学机制对于开发新型治疗方法和提高患者生存预测的准确性至关重要。虽然之前的研究已通过当前的机器学习和深度学习方法利用基因表达和临床数据预测生存结果,但基因突变数据尽管是一个广受认可的指标,却很少被纳入其中,原因在于其信息有限、基因关系表示不充分以及数据稀疏,这对当前生存分析方法的稳健性、有效性和可解释性产生了负面影响。为了克服突变数据稀少带来的挑战,我们提出了一种新颖的深度学习神经网络框架--RCoxNet,它将随机行走与重启(RWR)算法与深度学习考克斯比例危害模型整合在一起。通过将该框架应用于来自 cBioportal 的突变数据,我们的模型在四种癌症类型中实现了 0.62+-0.05 的平均一致性指数,优于现有的深度神经网络模型。此外,我们还发现了区分预测的高风险和低风险患者的关键临床特征,这些特征的相关性得到了先前研究的部分支持。
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