Diffusion histology imaging combining diffusion basis spectrum imaging (DBSI) and machine learning improves detection and classification of glioblastoma pathology

Zezhong Ye, Richard L. Price, Xiran Liu, Joshua Lin, Qingsong Yang, Peng Sun, Anthony T. Wu, Liang Wang, Rowland H. Han, Chunyu Song, Ruimeng Yang, Sam E. Gary, Diane D. Mao, Michael Wallendorf, Jian L. Campian, Jr Shin Li, Sonika Dahiya, Albert H. Kim, Sheng Kwei Song

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Purpose: Glioblastoma (GBM) is one of the deadliest cancers with no cure. While conventional MRI has been widely adopted to examine GBM clinically, accurate neuroimaging assessment of tumor histopathology for improved diagnosis, surgical planning, and treatment evaluation remains an unmet need in the clinical management of GBMs. Experimental Design: We employ a novel diffusion histology imaging (DHI) approach, combining diffusion basis spectrum imaging (DBSI) and machine learning, to detect, differentiate, and quantify areas of high cellularity, tumor necrosis, and tumor infiltration in GBM. Results: Gadolinium-enhanced T1-weighted or hyperintense fluid-attenuated inversion recovery failed to reflect the morphologic complexity underlying tumor in patients with GBM. Contrary to the conventional wisdom that apparent diffusion coefficient (ADC) negatively correlates with increased tumor cellularity, we demonstrate disagreement between ADC and histologically confirmed tumor cellularity in GBM specimens, whereas DBSI-derived restricted isotropic diffusion fraction positively correlated with tumor cellularity in the same specimens. By incorporating DBSI metrics as classifiers for a supervised machine learning algorithm, we accurately predicted high tumor cellularity, tumor necrosis, and tumor infiltration with 87.5%, 89.0%, and 93.4% accuracy, respectively. Conclusions: Our results suggest that DHI could serve as a favorable alternative to current neuroimaging techniques in guiding biopsy or surgery as well as monitoring therapeutic response in the treatment of GBM.

Original languageEnglish
Pages (from-to)5388-5399
Number of pages12
JournalClinical Cancer Research
Volume26
Issue number20
DOIs
StatePublished - Oct 15 2020

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