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Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study
Radiation therapy for patients with non‐small‐cell lung cancer is hampered by acute radiation‐induced toxicity in the esophagus. This study aims to validate that optical coherence tomography (OCT), a minimally invasive imaging technique with high resolution (~10 μm), is able to visualize and monitor...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY‐VCH Verlag GmbH & Co. KGaA
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065648/ https://www.ncbi.nlm.nih.gov/pubmed/31058437 http://dx.doi.org/10.1002/jbio.201800440 |
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author | Jelvehgaran, Pouya de Bruin, Daniel M. Khmelinskii, Artem Borst, Gerben Steinberg, Jeffrey D. Song, Ji‐Ying de Vos, Judith van Leeuwen, Ton G. Alderliesten, Tanja de Boer, Johannes F. van Herk, Marcel |
author_facet | Jelvehgaran, Pouya de Bruin, Daniel M. Khmelinskii, Artem Borst, Gerben Steinberg, Jeffrey D. Song, Ji‐Ying de Vos, Judith van Leeuwen, Ton G. Alderliesten, Tanja de Boer, Johannes F. van Herk, Marcel |
author_sort | Jelvehgaran, Pouya |
collection | PubMed |
description | Radiation therapy for patients with non‐small‐cell lung cancer is hampered by acute radiation‐induced toxicity in the esophagus. This study aims to validate that optical coherence tomography (OCT), a minimally invasive imaging technique with high resolution (~10 μm), is able to visualize and monitor acute radiation‐induced esophageal damage (ARIED) in mice. We compare our findings with histopathology as the gold standard. Irradiated mice receive a single dose of 40 Gy at proximal and distal spots of the esophagus of 10.0 mm in diameter. We scan mice using OCT at two, three, and seven days post‐irradiation. In OCT analysis, we define ARIED as a presence of distorted esophageal layering, change in backscattering signal properties, or change in the esophageal wall thickness. The average esophageal wall thickness is 0.53 mm larger on OCT when ARIED is present based on histopathology. The overall sensitivity and specificity of OCT to detect ARIED compared to histopathology are 94% and 47%, respectively. However, the overall sensitivity of OCT to assess ARIED is 100% seven days post‐irradiation. We validate the capability of OCT to detect ARIED induced by high doses in mice. Nevertheless, clinical studies are required to assess the potential role of OCT to visualize ARIED in humans. [Image: see text] |
format | Online Article Text |
id | pubmed-7065648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | WILEY‐VCH Verlag GmbH & Co. KGaA |
record_format | MEDLINE/PubMed |
spelling | pubmed-70656482020-03-16 Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study Jelvehgaran, Pouya de Bruin, Daniel M. Khmelinskii, Artem Borst, Gerben Steinberg, Jeffrey D. Song, Ji‐Ying de Vos, Judith van Leeuwen, Ton G. Alderliesten, Tanja de Boer, Johannes F. van Herk, Marcel J Biophotonics Letters Radiation therapy for patients with non‐small‐cell lung cancer is hampered by acute radiation‐induced toxicity in the esophagus. This study aims to validate that optical coherence tomography (OCT), a minimally invasive imaging technique with high resolution (~10 μm), is able to visualize and monitor acute radiation‐induced esophageal damage (ARIED) in mice. We compare our findings with histopathology as the gold standard. Irradiated mice receive a single dose of 40 Gy at proximal and distal spots of the esophagus of 10.0 mm in diameter. We scan mice using OCT at two, three, and seven days post‐irradiation. In OCT analysis, we define ARIED as a presence of distorted esophageal layering, change in backscattering signal properties, or change in the esophageal wall thickness. The average esophageal wall thickness is 0.53 mm larger on OCT when ARIED is present based on histopathology. The overall sensitivity and specificity of OCT to detect ARIED compared to histopathology are 94% and 47%, respectively. However, the overall sensitivity of OCT to assess ARIED is 100% seven days post‐irradiation. We validate the capability of OCT to detect ARIED induced by high doses in mice. Nevertheless, clinical studies are required to assess the potential role of OCT to visualize ARIED in humans. [Image: see text] WILEY‐VCH Verlag GmbH & Co. KGaA 2019-06-26 2019-09 /pmc/articles/PMC7065648/ /pubmed/31058437 http://dx.doi.org/10.1002/jbio.201800440 Text en © 2019 The Authors. Journal of Biophotonics published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Letters Jelvehgaran, Pouya de Bruin, Daniel M. Khmelinskii, Artem Borst, Gerben Steinberg, Jeffrey D. Song, Ji‐Ying de Vos, Judith van Leeuwen, Ton G. Alderliesten, Tanja de Boer, Johannes F. van Herk, Marcel Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title | Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title_full | Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title_fullStr | Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title_full_unstemmed | Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title_short | Optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: A validation study |
title_sort | optical coherence tomography to detect acute esophageal radiation‐induced damage in mice: a validation study |
topic | Letters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7065648/ https://www.ncbi.nlm.nih.gov/pubmed/31058437 http://dx.doi.org/10.1002/jbio.201800440 |
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