TY - JOUR
T1 - Diffusion histology imaging combining diffusion basis spectrum imaging (DBSI) and machine learning improves detection and classification of glioblastoma pathology
AU - Ye, Zezhong
AU - Price, Richard L.
AU - Liu, Xiran
AU - Lin, Joshua
AU - Yang, Qingsong
AU - Sun, Peng
AU - Wu, Anthony T.
AU - Wang, Liang
AU - Han, Rowland H.
AU - Song, Chunyu
AU - Yang, Ruimeng
AU - Gary, Sam E.
AU - Mao, Diane D.
AU - Wallendorf, Michael
AU - Campian, Jian L.
AU - Li, Jr Shin
AU - Dahiya, Sonika
AU - Kim, Albert H.
AU - Song, Sheng Kwei
N1 - Funding Information:
This work was supported in part by NIH (R01-NS047592, P01-NS059560, and U01-EY025500 to S.-K. Song, and R01-NS094670 to A.H. Kim), The Christopher Davidson and Knight Family Fund (to A.H. Kim), the Duesenberg Research Fund (to A.H. Kim), National Multiple Sclerosis Society (RG 1701-26617 to S.-K. Song), The Fundamental Research Funds for the Central Universities (SCUT 2018MS23 to R. Yang), Natural Science Foundation of Guangdong Province in China (2018A030313282 to R. Yang), and National Natural Science Foundation of China (81971574 to R. Yang).
Funding Information:
J.L. Campian reports grants from NeoImmuneTech (research fund) and other from AbbVie (spouse received speaker fee from AbbVie) outside the submitted work. A.H. Kim reports grants from NIH/NINDS (R01-NS094670) during the conduct of the study, as well as grants from Monteris Medical (laser therapy grant, unrelated to this study), Stryker (dural substitute grant, unrelated to this study), and Collagen Matrix (dural substitute grant, unrelated to this study), and personal fees from Monteris Medical (consulting) outside the submitted work. S.-K. Song has ownership of Cancer Vision LLC but did not receive any types of support including grants, payments, or fees from the company. No potential conflicts of interest were disclosed by the other authors.
Publisher Copyright:
© 2020 American Association for Cancer Research.
PY - 2020/10/15
Y1 - 2020/10/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85092086916&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-20-0736
DO - 10.1158/1078-0432.CCR-20-0736
M3 - Article
C2 - 32694155
AN - SCOPUS:85092086916
SN - 1078-0432
VL - 26
SP - 5388
EP - 5399
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 20
ER -