Biologically informed deep neural networks provide quantitative assessment of intratumoral heterogeneity in post treatment glioblastoma

Intratumoral heterogeneity poses a significant challenge to the diagnosis and treatment of recurrent glioblastoma. This study addresses the need for non-invasive approaches to map heterogeneous landscape of histopathological alterations throughout the entire lesion for each patient. We developed BioNet, a biologically-informed neural network, to predict regional distributions of two primary tissue-specific gene modules: proliferating tumor (Pro) and reactive/inflammatory cells (Inf). BioNet significantly outperforms existing methods (p < 2e-26). In cross-validation, BioNet achieved AUCs of 0.80 (Pro) and 0.81 (Inf), with accuracies of 80% and 75%, respectively. In blind tests, BioNet achieved AUCs of 0.80 (Pro) and 0.76 (Inf), with accuracies of 81% and 74%. Competing methods had AUCs lower or around 0.6 and accuracies lower or around 70%. BioNet's voxel-level prediction maps reveal intratumoral heterogeneity, potentially improving biopsy targeting and treatment evaluation. This non-invasive approach facilitates regular monitoring and timely therapeutic adjustments, highlighting the role of ML in precision medicine.

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Publication Details

Journal
npj Digital Medicine
Published
2024-10-19
DOI
https://doi.org/10.1038/s41746-024-01277-4
Citations
3
Primary Topic
Glioma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
1.31

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article

Biologically informed deep neural networks provide quantitative assessment of intratumoral heterogeneity in post treatment glioblastoma

Deborah Boyett, Kristin R. Swanson, Hairong Wang, Nhan L. Tran et al.
3 citations
npj Digital Medicine
Glioma Diagnosis and Treatment
1.31
article

Biologically informed deep neural networks provide quantitative assessment of intratumoral heterogeneity in post treatment glioblastoma

Deborah Boyett, Kristin R. Swanson, Hairong Wang, Nhan L. Tran, Kyle Singleton, Akshay Save, Lisa Paulson, Petros Petridis, Peter Canoll, Andrea Hawkins‐Daarud, Jeffrey N. Bruce, Leland Hu, William Savage, Jack Grinband, Osama Al‐Dalahmah, Michael Argenziano, Hyunsoo Yoon, Pamela Jackson, Jing Li
article en
3 citations

Abstract

Intratumoral heterogeneity poses a significant challenge to the diagnosis and treatment of recurrent glioblastoma. This study addresses the need for non-invasive approaches to map heterogeneous landscape of histopathological alterations throughout the entire lesion for each patient. We developed BioNet, a biologically-informed neural network, to predict regional distributions of two primary tissue-specific gene modules: proliferating tumor (Pro) and reactive/inflammatory cells (Inf). BioNet significantly outperforms existing methods (p < 2e-26). In cross-validation, BioNet achieved AUCs of 0.80 (Pro) and 0.81 (Inf), with accuracies of 80% and 75%, respectively. In blind tests, BioNet achieved AUCs of 0.80 (Pro) and 0.76 (Inf), with accuracies of 81% and 74%. Competing methods had AUCs lower or around 0.6 and accuracies lower or around 70%. BioNet's voxel-level prediction maps reveal intratumoral heterogeneity, potentially improving biopsy targeting and treatment evaluation. This non-invasive approach facilitates regular monitoring and timely therapeutic adjustments, highlighting the role of ML in precision medicine.

npj Digital MedicineVol. 7(1)
Georgia Institute of Technology (US), Yonsei University (KR), Columbia University Irving Medical Center (US), Mayo Clinic Hospital (US), Mayo Clinic in Florida (US), Neurological Surgery (US), New York University (US)
National Science Foundation, National Institutes of Health, National Cancer Institute, National Institute of Neurological Disorders and Stroke
Good health and well-being
Openalex Percentile: Top 18%
Glioma Diagnosis and Treatment
1.31
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