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LTARM: A novel temporal association rule mining method to understand toxicities in a routine cancer treatment

机译:LTARM:一种新型的时间关联规则挖掘方法,用于了解常规癌症治疗中的毒性

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Cancer is a worldwide problem and one of the leading causes of death. Increasing prevalence of cancer, particularly in developing countries, demands better understandings of the effectiveness and adverse consequences of different cancer treatment regimes in real patient populations. Current understandings of cancer treatment toxicities are often derived from either "clean" patient cohorts or coarse population statistics. Thus, it is difficult to get up-to-date and local assessments of treatment toxicities for specific cancer centers. To address these problems, we propose a novel and efficient method for discovering toxicity progression patterns in the form of temporal association rules (TARs). A temporal association rule is defined as a rule where the diagnosis codes in the right hand side (e.g., a combination of toxicities/complications) are temporally occurred after the diagnosis codes in the left hand side (e.g., a particular type of cancer treatment). Our method develops a lattice structure to efficiently discover TARs. More specifically, the lattice structure is first constructed to store all frequent diagnosis codes in the dataset. It is then traversed using the paternity relations among nodes to generate TARs. Our extensive experiments show the effectiveness of the proposed method in discovering major toxicity patterns in comparison with the temporal comorbidity analysis. In addition, our method significantly outperforms existing methods for mining TARs in terms of runtime. (C) 2018 Elsevier B.V. All rights reserved.
机译:癌症是一个世界性问题,也是主要的死亡原因之一。癌症患病率的增加,尤其是在发展中国家,要求对实际患者人群中不同癌症治疗方案的有效性和不良后果有更好的了解。当前对癌症治疗毒性的了解通常来自“干净的”患者队列或粗略的人口统计数据。因此,很难获得针对特定癌症中心的治疗毒性的最新和本地评估。为了解决这些问题,我们提出了一种新颖而有效的方法,以时间关联规则(TAR)的形式发现毒性进展模式。时间关联规则被定义为在左侧的诊断代码之后(例如,特定类型的癌症治疗)在时间上出现右侧的诊断代码(例如,毒性/并发症的组合)的规则。 。我们的方法开发出一种晶格结构来有效发现TAR。更具体地说,首先构造晶格结构以将所有频繁的诊断代码存储在数据集中。然后使用节点之间的亲子关系遍历它以生成TAR。我们广泛的实验表明,与时间合并症分析相比,该方法在发现主要毒性模式方面是有效的。此外,在运行时方面,我们的方法大大优于现有的TAR挖掘方法。 (C)2018 Elsevier B.V.保留所有权利。

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