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Quantification of multiplexed fluorescence peptides in human esophagus for early cancer detection (Conference Presentation)

Paper Abstract

Fluorescence endoscopy is emerging for guiding biopsy and early cancer detection in the gastrointestinal tract. A multimodal scanning fiber endoscope (mmSFE) with 2 fluorescence labeled peptides is designed to image overexpressed biomarkers associated with esophageal adenocarcinoma (EAC) and high-grade dysplasia (HGD), thus detecting early neoplasia. Quantification of multiplexed fluorescence images is critical, which ‘red-flags’ suspicious regions and supports diagnosis. The Target/Background (T/B) ratio is calculated to quantitatively evaluate fluorescence images. However T/B ratios are based on fluorescence intensities alone, so adding morphological features can be critical to providing evidence for diagnosis. Moreover, currently the T/B ratio is calculated for a single fluorescence channel. A protocol for multiplexed fluorescence quantification is needed. Materials and Methods: Peptides targeting EGFR and ErbB2 are labeled with NIR fluorescence Cy5 and IRdye800, respectively. A mmSFE with 2.4mm flexible shaft and wide-field forward-view imaging is designed to image these two near-infrared fluorophores with an additional reflectance channel for anatomical identification. In first-in-human clinical trials the two peptides are topically sprayed, briefly incubated, and then rinsed in subjects at high risk of EAC. Both fluorescence channels were captured simultaneously with the co-registered reflectance channel at 30Hz. After removing artifacts, frames were manually selected using morphological features. T/B ratios were then calculated for all fluorescence channels in selected frames. Results and Conclusions: T/B ratios for HGD subjects are greater than for healthy subjects in at least one of the fluorescence channels. Future work will design algorithms to automatically select suspicious regions based on morphological features. More analysis will be performed based on co-registered fluorescence channels.

Paper Details

Date Published: 4 March 2019
Proc. SPIE 10854, Endoscopic Microscopy XIV, 1085410 (4 March 2019); doi: 10.1117/12.2511815
Show Author Affiliations
Yang Jiang, Univ. of Washington (United States)
Jing Chen, University of Michigan (United States)
Danielle K. Turgeon, Univ. of Michigan (United States)
Joel H. Rubenstein, Univ. of Michigan (United States)
Thomas D. Wang, Univ. of Michigan (United States)
Eric J. Seibel, Univ. of Washington (United States)

Published in SPIE Proceedings Vol. 10854:
Endoscopic Microscopy XIV
Guillermo J. Tearney M.D.; Thomas D. Wang; Melissa J. Suter, Editor(s)

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