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Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging

A real-time optical biopsy, which could determine tissue histopathology, would be of extraordinary benefit to staging laparoscopy for gastric cancer with serosal invasion (T4) that requires downstage treatment. We investigated the feasibility of using multiphoton imaging to perform a real-time optic...

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Autores principales: Yan, Jun, Zheng, Yu, Zheng, Xiaoling, Liu, Zhangyuanzhu, Liu, Wenju, Chen, Dexin, Dong, Xiaoyu, Li, Kai, Liu, Xiumin, Chen, Gang, Lu, Jianping, Chen, Jianxin, Zhuo, Shuangmu, Li, Guoxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976383/
https://www.ncbi.nlm.nih.gov/pubmed/27499365
http://dx.doi.org/10.1038/srep31004
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author Yan, Jun
Zheng, Yu
Zheng, Xiaoling
Liu, Zhangyuanzhu
Liu, Wenju
Chen, Dexin
Dong, Xiaoyu
Li, Kai
Liu, Xiumin
Chen, Gang
Lu, Jianping
Chen, Jianxin
Zhuo, Shuangmu
Li, Guoxin
author_facet Yan, Jun
Zheng, Yu
Zheng, Xiaoling
Liu, Zhangyuanzhu
Liu, Wenju
Chen, Dexin
Dong, Xiaoyu
Li, Kai
Liu, Xiumin
Chen, Gang
Lu, Jianping
Chen, Jianxin
Zhuo, Shuangmu
Li, Guoxin
author_sort Yan, Jun
collection PubMed
description A real-time optical biopsy, which could determine tissue histopathology, would be of extraordinary benefit to staging laparoscopy for gastric cancer with serosal invasion (T4) that requires downstage treatment. We investigated the feasibility of using multiphoton imaging to perform a real-time optical diagnosis of gastric cancer with or without serosal invasion. First, a pilot study was performed to establish the optical diagnostic features of gastric cancer with or without serosal invasion using multiphoton imaging compared with hematoxylin-eosin staining and Masson’s trichrome staining. Second, a blinded study was performed to compare the diagnostic sensitivity, specificity, and accuracy of multiphoton imaging and endoscopic ultrasonography (EUS) for T4 gastric cancer. In the pilot study, multiphoton imaging revealed collagen loss and degradation and cellular and nuclear pleomorphism in gastric cancer with serosal invasion. The collagen content in gastric cancer with or without serosal invasion was 0.36 ± 0.18 and 0.79 ± 0.16 (p < 0.001), respectively. In the blinded study, the sensitivity, specificity, and accuracy of EUS and multiphoton imaging for T4 gastric cancer were 70% and 90% (p = 0.029), 66.67% and 96.67% (p = 0.003), and 68.33% and 93.33% (p = 0.001), respectively. It is feasible to use multiphoton imaging to make a real-time optical diagnosis of gastric cancer with or without serosal invasion.
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spelling pubmed-49763832016-08-22 Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging Yan, Jun Zheng, Yu Zheng, Xiaoling Liu, Zhangyuanzhu Liu, Wenju Chen, Dexin Dong, Xiaoyu Li, Kai Liu, Xiumin Chen, Gang Lu, Jianping Chen, Jianxin Zhuo, Shuangmu Li, Guoxin Sci Rep Article A real-time optical biopsy, which could determine tissue histopathology, would be of extraordinary benefit to staging laparoscopy for gastric cancer with serosal invasion (T4) that requires downstage treatment. We investigated the feasibility of using multiphoton imaging to perform a real-time optical diagnosis of gastric cancer with or without serosal invasion. First, a pilot study was performed to establish the optical diagnostic features of gastric cancer with or without serosal invasion using multiphoton imaging compared with hematoxylin-eosin staining and Masson’s trichrome staining. Second, a blinded study was performed to compare the diagnostic sensitivity, specificity, and accuracy of multiphoton imaging and endoscopic ultrasonography (EUS) for T4 gastric cancer. In the pilot study, multiphoton imaging revealed collagen loss and degradation and cellular and nuclear pleomorphism in gastric cancer with serosal invasion. The collagen content in gastric cancer with or without serosal invasion was 0.36 ± 0.18 and 0.79 ± 0.16 (p < 0.001), respectively. In the blinded study, the sensitivity, specificity, and accuracy of EUS and multiphoton imaging for T4 gastric cancer were 70% and 90% (p = 0.029), 66.67% and 96.67% (p = 0.003), and 68.33% and 93.33% (p = 0.001), respectively. It is feasible to use multiphoton imaging to make a real-time optical diagnosis of gastric cancer with or without serosal invasion. Nature Publishing Group 2016-08-08 /pmc/articles/PMC4976383/ /pubmed/27499365 http://dx.doi.org/10.1038/srep31004 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yan, Jun
Zheng, Yu
Zheng, Xiaoling
Liu, Zhangyuanzhu
Liu, Wenju
Chen, Dexin
Dong, Xiaoyu
Li, Kai
Liu, Xiumin
Chen, Gang
Lu, Jianping
Chen, Jianxin
Zhuo, Shuangmu
Li, Guoxin
Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title_full Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title_fullStr Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title_full_unstemmed Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title_short Real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
title_sort real-time optical diagnosis of gastric cancer with serosal invasion using multiphoton imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976383/
https://www.ncbi.nlm.nih.gov/pubmed/27499365
http://dx.doi.org/10.1038/srep31004
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