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A comparative study of survival models for breast cancer prognostication based on microarray data: does a single gene beat them all?

机译:基于微阵列数据的乳腺癌预后生存模型的比较研究:单个基因能否击败它们?

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Motivation: Survival prediction of breast cancer (BC) patients independently of treatment, also known as prognostication, is a complex task since clinically similar breast tumors, in addition to be molecularly heterogeneous, may exhibit different clinical outcomes. In recent years, the analysis of gene expression profiles by means of sophisticated data mining tools emerged as a promising technology to bring additional insights into BC biology and to improve the quality of prognostication. The aim of this work is to assess quantitatively the accuracy of prediction obtained with state-of-the-art data analysis techniques for BC microarray data through an independent and thorough framework.Results: Due to the large number of variables, the reduced amount of samples and the high degree of noise, complex prediction methods are highly exposed to performance degradation despite the use of cross-validation techniques. Our analysis shows that the most complex methods are not significantly better than the simplest one, a univariate model relying on a single proliferation gene. This result suggests that proliferation might be the most relevant biological process for BC prognostication and that the loss of interpretability deriving from the use of overcomplex methods may be not sufficiently counterbalanced by an improvement of the quality of prediction.
机译:动机:乳腺癌(BC)患者的独立于治疗的生存预测(也称为预后)是一项复杂的任务,因为除了分子异质性以外,临床上相似的乳腺肿瘤可能表现出不同的临床结局。近年来,借助复杂的数据挖掘工具对基因表达谱进行分析成为一种有前途的技术,可为BC生物学带来更多见解,并改善预后质量。这项工作的目的是通过一个独立而透彻的框架来定量评估使用最新数据分析技术对BC微阵列数据进行预测的准确性。结果:由于变量众多,减少的预测数量尽管使用了交叉验证技术,但由于样本和高噪声水平,复杂的预测方法极易遭受性能下降的影响。我们的分析表明,最复杂的方法并不比最简单的方法显着好,最简单的方法是依赖单个增殖基因的单变量模型。该结果表明,增殖可能是与BC预后最相关的生物学过程,而通过使用过度复杂的方法而导致的可解释性的丧失可能无法通过预测质量的改善而得到充分抵消。

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