Abstract

In this paper, we address two long-standing radio-genomic challenges in glioma subtype and survival prediction: (1) how to leverage large amounts of unlabeled magnetic resonance (MR) imaging data and (2) how to unite MR data and genomic data. We propose a novel application of multi-task learning (MTL) that leverages unlabeled MR data by jointly learning an auxiliary tumor segmentation task with glioma subtype prediction and that can learn from patients with and without genomic data. We analyze multi-parametric MR data from 542 patients in the combined training, validation, and testing sets of the 2018 Multimodal Brain Tumor Segmentation Challenge and somatic copy number alteration (SCNA) data from 1090 patients in The Cancer Genome Atlas' (TCGA) lower-grade glioma and glioblastoma projects. Our MTL model significantly outperforms comparable classification models trained only on labeled MR data for both IDH1/2 mutation and 1p/19q co-deletion subtype prediction tasks. We also show that embeddings produced by our MTL models improve survival predictions beyond MR or SCNA on their own. Our code is available at https://github.com/nknuecht/glioma_mtl.

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