Hyperpolarized Magnetic Resonance Imaging, Nuclear Magnetic Resonance Metabolomics, and Artificial Intelligence to Interrogate the Metabolic Evolution of Glioblastoma

Author:

Hsieh Kang Lin1ORCID,Chen Qing2,Salzillo Travis C.3ORCID,Zhang Jian2,Jiang Xiaoqian4,Bhattacharya Pratip K.5ORCID,Shams Shyan4

Affiliation:

1. Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2. Department of Computer Science, Louisiana State University, Baton Rouge, LA 70803, USA

3. Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

4. Department of Health Data Science and Artificial Intelligence, McWilliams School of Biomedical Informatics at UTHealth Houston, Houston, TX 77030, USA

5. Department of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

Abstract

Glioblastoma (GBM) is a malignant Grade VI cancer type with a median survival duration of only 8–16 months. Earlier detection of GBM could enable more effective treatment. Hyperpolarized magnetic resonance spectroscopy (HPMRS) could detect GBM earlier than conventional anatomical MRI in glioblastoma murine models. We further investigated whether artificial intelligence (A.I.) could detect GBM earlier than HPMRS. We developed a deep learning model that combines multiple modalities of cancer data to predict tumor progression, assess treatment effects, and to reconstruct in vivo metabolomic information from ex vivo data. Our model can detect GBM progression two weeks earlier than conventional MRIs and a week earlier than HPMRS alone. Our model accurately predicted in vivo biomarkers from HPMRS, and the results inferred biological relevance. Additionally, the model showed potential for examining treatment effects. Our model successfully detected tumor progression two weeks earlier than conventional MRIs and accurately predicted in vivo biomarkers using ex vivo information such as conventional MRIs, HPMRS, and tumor size data. The accuracy of these predictions is consistent with biological relevance.

Funder

Cancer Prevention and Research Institute of Texas

CPRIT Research Training Award

The University of Texas Health Science Center at Houston Center for Clinical and Translational Sciences TL1 Program

CPRIT Scholar in Cancer Research

Christopher Sarofim Family Professorship

UT Stars award

UTHealth startup

National Institute of Health

CPRIT

National Institute of Biomedical Imaging and Engineering

NIH

Department of Defense

Melanoma Research Alliance

MD Anderson Institutional Research Grants

MD Anderson Institutional Startup

Brain SPORE Developmental Research Award

Rivkin Center

Mike Slive and Koch Foundations

University of Texas MD Anderson Cancer Center

Ovarian Cancer Research Alliance

Publisher

MDPI AG

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