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Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples

The primary line of therapy for high-grade brain tumor is surgical resection, however, identifying tumor margins in vivo remains a major challenge. Despite the progress in computer-assisted imaging techniques, biopsy analysis remains the standard diagnostic tool when it comes to delineating tumor ma...

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Autores principales: Poulon, Fanny, Pallud, Johan, Varlet, Pascale, Zanello, Marc, Chretien, Fabrice, Dezamis, Edouard, Abi-Lahoud, Georges, Nataf, François, Turak, Baris, Devaux, Bertrand, Abi Haidar, Darine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173695/
https://www.ncbi.nlm.nih.gov/pubmed/30291269
http://dx.doi.org/10.1038/s41598-018-33134-2
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author Poulon, Fanny
Pallud, Johan
Varlet, Pascale
Zanello, Marc
Chretien, Fabrice
Dezamis, Edouard
Abi-Lahoud, Georges
Nataf, François
Turak, Baris
Devaux, Bertrand
Abi Haidar, Darine
author_facet Poulon, Fanny
Pallud, Johan
Varlet, Pascale
Zanello, Marc
Chretien, Fabrice
Dezamis, Edouard
Abi-Lahoud, Georges
Nataf, François
Turak, Baris
Devaux, Bertrand
Abi Haidar, Darine
author_sort Poulon, Fanny
collection PubMed
description The primary line of therapy for high-grade brain tumor is surgical resection, however, identifying tumor margins in vivo remains a major challenge. Despite the progress in computer-assisted imaging techniques, biopsy analysis remains the standard diagnostic tool when it comes to delineating tumor margins. Our group aims to answer this challenge by exploiting optical imaging of endogenous fluorescence in order to provide a reliable and reproducible diagnosis close to neuropathology. In this study, we first establish the ability of two-photon microscopy (TPM) to discriminate normal brain tissue from glioblastomas and brain metastasis using the endogenous fluorescence response of fresh human brain sample. Two-photon fluorescence images were compared to gold standard neuropathology. “Blind” diagnosis realized by a neuropathologist on a group of TPM images show a good sensitivity, 100%, and specificity, 50% to discriminate non tumoral brain tissue versus glioblastoma or brain metastasis. Quantitative analysis on spectral and fluorescence lifetime measurements resulted in building a scoring system to discriminate brain tissue samples.
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spelling pubmed-61736952018-10-09 Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples Poulon, Fanny Pallud, Johan Varlet, Pascale Zanello, Marc Chretien, Fabrice Dezamis, Edouard Abi-Lahoud, Georges Nataf, François Turak, Baris Devaux, Bertrand Abi Haidar, Darine Sci Rep Article The primary line of therapy for high-grade brain tumor is surgical resection, however, identifying tumor margins in vivo remains a major challenge. Despite the progress in computer-assisted imaging techniques, biopsy analysis remains the standard diagnostic tool when it comes to delineating tumor margins. Our group aims to answer this challenge by exploiting optical imaging of endogenous fluorescence in order to provide a reliable and reproducible diagnosis close to neuropathology. In this study, we first establish the ability of two-photon microscopy (TPM) to discriminate normal brain tissue from glioblastomas and brain metastasis using the endogenous fluorescence response of fresh human brain sample. Two-photon fluorescence images were compared to gold standard neuropathology. “Blind” diagnosis realized by a neuropathologist on a group of TPM images show a good sensitivity, 100%, and specificity, 50% to discriminate non tumoral brain tissue versus glioblastoma or brain metastasis. Quantitative analysis on spectral and fluorescence lifetime measurements resulted in building a scoring system to discriminate brain tissue samples. Nature Publishing Group UK 2018-10-05 /pmc/articles/PMC6173695/ /pubmed/30291269 http://dx.doi.org/10.1038/s41598-018-33134-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Poulon, Fanny
Pallud, Johan
Varlet, Pascale
Zanello, Marc
Chretien, Fabrice
Dezamis, Edouard
Abi-Lahoud, Georges
Nataf, François
Turak, Baris
Devaux, Bertrand
Abi Haidar, Darine
Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title_full Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title_fullStr Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title_full_unstemmed Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title_short Real-time Brain Tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
title_sort real-time brain tumor imaging with endogenous fluorophores: a diagnosis proof-of-concept study on fresh human samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6173695/
https://www.ncbi.nlm.nih.gov/pubmed/30291269
http://dx.doi.org/10.1038/s41598-018-33134-2
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