QMAICVLGIVMar 31, 2022

Optimize Deep Learning Models for Prediction of Gene Mutations Using Unsupervised Clustering

arXiv:2204.01593v2
Originality Highly original
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This work addresses the challenge of accurately predicting gene mutations in cancer diagnostics, offering a novel approach that outperforms baseline methods and reveals insights into tumor microenvironment heterogeneity.

The authors tackled the problem of predicting gene mutations from whole-slide pathology images by proposing an unsupervised clustering-based method to identify predictive patches, which improved prediction accuracy across three cancer types compared to existing approaches.

Deep learning has become the mainstream methodological choice for analyzing and interpreting whole-slide digital pathology images (WSIs). It is commonly assumed that tumor regions carry most predictive information. In this paper, we proposed an unsupervised clustering-based multiple-instance learning, and apply our method to develop deep-learning models for prediction of gene mutations using WSIs from three cancer types in The Cancer Genome Atlas (TCGA) studies (CRC, LUAD, and HNSCC). We showed that unsupervised clustering of image patches could help identify predictive patches, exclude patches lack of predictive information, and therefore improve prediction on gene mutations in all three different cancer types, compared with the WSI based method without selection of image patches and models based on only tumor regions. Additionally, our proposed algorithm outperformed two recently published baseline algorithms leveraging unsupervised clustering to assist model prediction. The unsupervised-clustering-based approach for mutation prediction allows identification of the spatial regions related to mutation of a specific gene via the resolved probability scores, highlighting the heterogeneity of a predicted genotype in the tumor microenvironment. Finally, our study also demonstrated that selection of tumor regions of WSIs is not always the best way to identify patches for prediction of gene mutations, and other tissue types in the tumor micro-environment may provide better prediction ability for gene mutations than tumor tissues.

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