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Proceedings Paper

In vivo metabolic imaging of early stage oral cancer and dysplasia based on autofluorescence lifetime endoscopy (Conference Presentation)
Author(s): Elvis Duran; Dae Yon Hwang; Shuna Cheng; Rodrigo Cuenca; Bilal H. Malik; Kristen C. Maitland; John M. Wright; Yi-Shing Lisa Cheng; Beena Ahmed; Javier A Jo
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Paper Abstract

Increased metabolic activity, a hallmark of epithelial cell malignant transformation, induces subtle changes in the oral tissue autofluorescence. The optical “redox-ratio”, defined as the autofluorescence intensity of NADH divided by that of FAD, is sensitive to changes in the cellular metabolic rate. A decrease in the redox-ratio indicates increased cellular metabolic activity, as is typically observed in malignant cells. Specific changes in the fluorescence lifetime of both NADH and FAD have also been associated with increased metabolic activity in malignant oral epithelial cells. We therefore hypothesized that more specific biomarkers of oral cancer and dysplasia can more accurately be quantified by endogenous fluorescence lifetime imaging (FLIM). In this work, FLIM images of benign, dysplastic and early stage cancerous oral lesions from 52 patients were acquired at three emission channels (390±20nm, 452±22.5nm and >500nm) using a handheld multispectral FLIM endoscope. For each pixel, the fluorescence decays collected at the three emission bands were analyzed using a biexponential decay model, resulting on 16 FLIM-derived parameters per pixel. Statistical analysis was performed on each of the computed FLIM parameters (Wilcoxon test: Normal vs. Benign, Normal vs. Dysplasia/Cancer; Mann-Whitney test: Benign vs. Dysplasia/Cancer). Results from this analysis revealed that FLIM-derived parameters associated with collagen lifetime, NADH lifetime, FAD autofluorescence, and the optical redox ratio were statistical different between dysplastic/cancerous vs. benign oral lesions. This study provides the first demonstration for the clinical imaging of autofluorescence biochemical and metabolic biomarkers of oral epithelial cancer and dysplasia, which could potentially enable early detection of oral cancer.

Paper Details

Date Published: 14 March 2018
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Proc. SPIE 10469, Optical Imaging, Therapeutics, and Advanced Technology in Head and Neck Surgery and Otolaryngology 2018, 1046913 (14 March 2018); doi: 10.1117/12.2287472
Show Author Affiliations
Elvis Duran, Texas A&M Univ. (United States)
Dae Yon Hwang, Texas A&M Univ (United States)
Shuna Cheng, Texas A&M Univ. (United States)
Rodrigo Cuenca, Texas A&M Univ. (United States)
Bilal H. Malik, Texas A&M Univ. (United States)
Kristen C. Maitland, Texas A&M Univ. (United States)
John M. Wright, Texas A&M Univ. College of Dentistry (United States)
Yi-Shing Lisa Cheng, Texas A&M Univ. College of Dentistry (United States)
Beena Ahmed, Texas A&M Univ. (Qatar)
Javier A Jo, Texas A&M Univ. (United States)


Published in SPIE Proceedings Vol. 10469:
Optical Imaging, Therapeutics, and Advanced Technology in Head and Neck Surgery and Otolaryngology 2018
Brian J. F. Wong; Justus F. Ilgner; Max J. Witjes, Editor(s)

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