Department of Biomedical Informatics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.
Center for Translational Bioinformatics, University of Pittsburgh, Pittsburgh, Pennsylvania.
Mol Cancer Res. 2018 Feb;16(2):269-278. doi: 10.1158/1541-7786.MCR-17-0378. Epub 2017 Nov 13.
Precision oncology involves identifying drugs that will effectively treat a tumor and then prescribing an optimal clinical treatment regimen. However, most first-line chemotherapy drugs do not have biomarkers to guide their application. For molecularly targeted drugs, using the genomic status of a drug target as a therapeutic indicator has limitations. In this study, machine learning methods (e.g., deep learning) were used to identify informative features from genome-scale omics data and to train classifiers for predicting the effectiveness of drugs in cancer cell lines. The methodology introduced here can accurately predict the efficacy of drugs, regardless of whether they are molecularly targeted or nonspecific chemotherapy drugs. This approach, on a per-drug basis, can identify sensitive cancer cells with an average sensitivity of 0.82 and specificity of 0.82; on a per-cell line basis, it can identify effective drugs with an average sensitivity of 0.80 and specificity of 0.82. This report describes a data-driven precision medicine approach that is not only generalizable but also optimizes therapeutic efficacy. The framework detailed herein, when successfully translated to clinical environments, could significantly broaden the scope of precision oncology beyond targeted therapies, benefiting an expanded proportion of cancer patients. .
精准肿瘤学涉及识别能够有效治疗肿瘤的药物,然后为患者制定最佳的临床治疗方案。然而,大多数一线化疗药物没有生物标志物来指导其应用。对于分子靶向药物,使用药物靶点的基因组状态作为治疗指标具有局限性。在这项研究中,使用机器学习方法(例如深度学习)从基因组规模的组学数据中识别信息特征,并训练分类器来预测药物在癌细胞系中的疗效。这里介绍的方法可以准确预测药物的疗效,无论这些药物是分子靶向药物还是非特异性化疗药物。这种基于药物的方法可以识别敏感性癌症细胞,平均敏感性为 0.82,特异性为 0.82;基于细胞系的方法可以识别有效药物,平均敏感性为 0.80,特异性为 0.82。本报告描述了一种数据驱动的精准医学方法,不仅具有通用性,而且还可以优化治疗效果。本文详细介绍的框架,如果成功转化为临床环境,可以将精准肿瘤学的范围大大扩展到靶向治疗之外,使更多比例的癌症患者受益。