Abstract

BackgroundPredicting the drug response of a patient is important for precision oncology. In recent studies, multi-omics data have been used to improve the prediction accuracy of drug response. Although multi-omics data are good resources for drug response prediction, the large dimension of data tends to hinder performance improvement. In this study, we aimed to develop a new method, which can effectively reduce the large dimension of data, based on the supervised deep learning model for predicting drug response.ResultsWe proposed a novel method called Supervised Feature Extraction Learning using Triplet loss (Super.FELT) for drug response prediction. Super.FELT consists of three stages, namely, feature selection, feature encoding using a supervised method, and binary classification of drug response (sensitive or resistant). We used multi-omics data including mutation, copy number aberration, and gene expression, and these were obtained from cell lines [Genomics of Drug Sensitivity in Cancer (GDSC), Cancer Cell Line Encyclopedia (CCLE), and Cancer Therapeutics Response Portal (CTRP)], patient-derived tumor xenografts (PDX), and The Cancer Genome Atlas (TCGA). GDSC was used for training and cross-validation tests, and CCLE, CTRP, PDX, and TCGA were used for external validation. We performed ablation studies for the three stages and verified that the use of multi-omics data guarantees better performance of drug response prediction. Our results verified that Super.FELT outperformed the other methods at external validation on PDX and TCGA and was good at cross-validation on GDSC and external validation on CCLE and CTRP. In addition, through our experiments, we confirmed that using multi-omics data is useful for external non-cell line data.ConclusionBy separating the three stages, Super.FELT achieved better performance than the other methods. Through our results, we found that it is important to train encoders and a classifier independently, especially for external test on PDX and TCGA. Moreover, although gene expression is the most powerful data on cell line data, multi-omics promises better performance for external validation on non-cell line data than gene expression data. Source codes of Super.FELT are available at https://github.com/DMCB-GIST/Super.FELT.

Highlights

  • Predicting the drug response of a patient is important for precision oncology

  • Our results showed that Super.FELT is superior to the other drug response prediction methods on external datasets

  • In the subsection ‘On Cell Line Encyclopedia (CCLE) and Cancer Therapeutics Response Portal (CTRP)’, we evaluated how well Super.FELT works on external cell line data

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Summary

Introduction

Predicting the drug response of a patient is important for precision oncology. In recent studies, multi-omics data have been used to improve the prediction accuracy of drug response. Large-scale omics data have been made publicly accessible, including Genomics of Drug Sensitivity in Cancer (GDSC) [4], Cancer Cell Line Encyclopedia (CCLE) [5], Cancer Therapeutics Response Portal (CTRP) [6], Patient-Derived tumor Xenografts (PDX) encyclopedia [7], and The Cancer Genome Atlas (TCGA) [8]. These datasets provide multi-omics data that consists of gene expression, somatic mutation and copy number aberration (CNA), and response to multiple drugs

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