Department of Biostatistics, Jiann-Ping Hsu College of Public Health, Georgia Southern University, Statesboro, GA, USA.
Department of Hematology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
BMC Cancer. 2018 May 10;18(1):551. doi: 10.1186/s12885-018-4483-6.
Multiple myeloma (MM), like other cancers, is caused by the accumulation of genetic abnormalities. Heterogeneity exists in the patients' response to treatments, for example, bortezomib. This urges efforts to identify biomarkers from numerous molecular features and build predictive models for identifying patients that can benefit from a certain treatment scheme. However, previous studies treated the multi-level ordinal drug response as a binary response where only responsive and non-responsive groups are considered.
It is desirable to directly analyze the multi-level drug response, rather than combining the response to two groups. In this study, we present a novel method to identify significantly associated biomarkers and then develop ordinal genomic classifier using the hierarchical ordinal logistic model. The proposed hierarchical ordinal logistic model employs the heavy-tailed Cauchy prior on the coefficients and is fitted by an efficient quasi-Newton algorithm.
We apply our hierarchical ordinal regression approach to analyze two publicly available datasets for MM with five-level drug response and numerous gene expression measures. Our results show that our method is able to identify genes associated with the multi-level drug response and to generate powerful predictive models for predicting the multi-level response.
The proposed method allows us to jointly fit numerous correlated predictors and thus build efficient models for predicting the multi-level drug response. The predictive model for the multi-level drug response can be more informative than the previous approaches. Thus, the proposed approach provides a powerful tool for predicting multi-level drug response and has important impact on cancer studies.
多发性骨髓瘤(MM)与其他癌症一样,是由遗传异常的积累引起的。患者对治疗的反应存在异质性,例如硼替佐米。这促使人们从众多分子特征中识别生物标志物,并建立预测模型,以识别可以从某种治疗方案中受益的患者。然而,以前的研究将多水平有序药物反应视为二元反应,仅考虑有反应和无反应的组。
直接分析多水平药物反应是理想的,而不是将反应组合为两组。在这项研究中,我们提出了一种新的方法来识别显著相关的生物标志物,然后使用层次有序逻辑模型开发有序基因组分类器。所提出的层次有序逻辑模型对系数采用重尾 Cauchy 先验,并通过有效的拟牛顿算法进行拟合。
我们将我们的层次有序回归方法应用于分析具有五级药物反应和众多基因表达测量的两个公开可用的 MM 数据集。我们的结果表明,我们的方法能够识别与多水平药物反应相关的基因,并生成强大的预测模型来预测多水平反应。
所提出的方法允许我们共同拟合众多相关预测因子,从而为预测多水平药物反应建立高效模型。多水平药物反应的预测模型比以前的方法更具信息量。因此,所提出的方法为预测多水平药物反应提供了强大的工具,并对癌症研究具有重要影响。