Title
Machine-learning assisted discrimination of precancerous and cancerous from healthy oral tissue based on multispectral autofluorescence lifetime imaging endoscopy
Date Issued
01 October 2021
Access level
open access
Resource Type
journal article
Author(s)
Duran-Sierra E.
Cheng S.
Cuenca R.
Ahmed B.
Ji J.
Yakovlev V.V.
Martinez M.
Al-Khalil M.
Al-Enazi H.
Lisa Cheng Y.S.
Wright J.
Busso C.
University of Oklahoma
Publisher(s)
MDPI
Abstract
Multispectral autofluorescence lifetime imaging (maFLIM) can be used to clinically image a plurality of metabolic and biochemical autofluorescence biomarkers of oral epithelial dysplasia and cancer. This study tested the hypothesis that maFLIM-derived autofluorescence biomarkers can be used in machine-learning (ML) models to discriminate dysplastic and cancerous from healthy oral tissue. Clinical widefield maFLIM endoscopy imaging of cancerous and dysplastic oral lesions was performed at two clinical centers. Endoscopic maFLIM images from 34 patients acquired at one of the clinical centers were used to optimize ML models for automated discrimination of dysplastic and cancerous from healthy oral tissue. A computer-aided detection system was developed and applied to a set of endoscopic maFLIM images from 23 patients acquired at the other clinical center, and its performance was quantified in terms of the area under the receiver operating characteristic curve (ROC-AUC). Discrimination of dysplastic and cancerous from healthy oral tissue was achieved with an ROC-AUC of 0.81. This study demonstrates the capabilities of widefield maFLIM endoscopy to clinically image autofluorescence biomarkers that can be used in ML models to discriminate dysplastic and cancerous from healthy oral tissue. Widefield maFLIM endoscopy thus holds potential for automated in situ detection of oral dysplasia and cancer.
Volume
13
Issue
19
Language
English
OCDE Knowledge area
Odontología, Cirugía oral, Medicina oral Oncología
Scopus EID
2-s2.0-85115375609
Source
Cancers
ISSN of the container
20726694
Sponsor(s)
Funding: This project was supported by the National Institutes of Health (NIH grants R01CA218739, 1R01GM127696, 1R21GM142107) and the Cancer Prevention and Research Institute of Texas (CPRIT grant RP180588). This work was also made possible by the grant NPRP8-1606-3-322 from the Qatar National Research Fund (a member of Qatar Foundation). The statements made herein are solely the responsibility of the authors. Research reported in this publication was also supported in part by the National Science Foundation (NSF) (DBI-1455671, CMMI-1826078), the Air Force Office of Scientific Research (AFOSR) (FA9550-15-1-0517, FA9550-20-1-0366, FA9550-20-1-0367), and the Army Medical Research Grant (W81XWH2010777), and by the Oklahoma Tobacco Settlement Endowment Trust awarded to the University of Oklahoma, Stephenson Cancer Center.
Sources of information: Directorio de Producción Científica Scopus