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Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity

Current clinical MRI techniques in rectal cancer have limited ability to examine cancer stroma. The differentiation of tumour from desmoplasia or fibrous tissue remains a challenge. Standard MRI cannot differentiate stage T1 from T2 (invasion of muscularis propria) tumours. Diffusion tensor imaging...

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Autores principales: Pham, Trang T., Stait-Gardner, Timothy, Lee, Cheok Soon, Barton, Michael, Graham, Petra L., Liney, Gary, Wong, Karen, Price, William S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597556/
https://www.ncbi.nlm.nih.gov/pubmed/31249325
http://dx.doi.org/10.1038/s41598-019-45450-2
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author Pham, Trang T.
Stait-Gardner, Timothy
Lee, Cheok Soon
Barton, Michael
Graham, Petra L.
Liney, Gary
Wong, Karen
Price, William S.
author_facet Pham, Trang T.
Stait-Gardner, Timothy
Lee, Cheok Soon
Barton, Michael
Graham, Petra L.
Liney, Gary
Wong, Karen
Price, William S.
author_sort Pham, Trang T.
collection PubMed
description Current clinical MRI techniques in rectal cancer have limited ability to examine cancer stroma. The differentiation of tumour from desmoplasia or fibrous tissue remains a challenge. Standard MRI cannot differentiate stage T1 from T2 (invasion of muscularis propria) tumours. Diffusion tensor imaging (DTI) can probe tissue structure and organisation (anisotropy). The purpose of this study was to examine DTI-MRI derived imaging markers of rectal cancer stromal heterogeneity and tumour extent ex vivo. DTI-MRI at ultra-high magnetic field (11.7 tesla) was used to examine the stromal microstructure of malignant and normal rectal tissue ex vivo, and the findings were correlated with histopathology. Images obtained from DTI-MRI (A0, apparent diffusion coefficient and fractional anisotropy (FA)) were used to probe rectal cancer stromal heterogeneity. FA provided the best discrimination between cancer and desmoplasia, fibrous tissue and muscularis propria. Cancer had relatively isotropic diffusion (mean FA 0.14), whereas desmoplasia (FA 0.31) and fibrous tissue (FA 0.34) had anisotropic diffusion with significantly higher FA than cancer (p < 0.001). Tumour was distinguished from muscularis propria (FA 0.61) which was highly anisotropic with higher FA than cancer (p < 0.001). This study showed that DTI-MRI can assist in more accurately defining tumour extent in rectal cancer.
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spelling pubmed-65975562019-07-09 Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity Pham, Trang T. Stait-Gardner, Timothy Lee, Cheok Soon Barton, Michael Graham, Petra L. Liney, Gary Wong, Karen Price, William S. Sci Rep Article Current clinical MRI techniques in rectal cancer have limited ability to examine cancer stroma. The differentiation of tumour from desmoplasia or fibrous tissue remains a challenge. Standard MRI cannot differentiate stage T1 from T2 (invasion of muscularis propria) tumours. Diffusion tensor imaging (DTI) can probe tissue structure and organisation (anisotropy). The purpose of this study was to examine DTI-MRI derived imaging markers of rectal cancer stromal heterogeneity and tumour extent ex vivo. DTI-MRI at ultra-high magnetic field (11.7 tesla) was used to examine the stromal microstructure of malignant and normal rectal tissue ex vivo, and the findings were correlated with histopathology. Images obtained from DTI-MRI (A0, apparent diffusion coefficient and fractional anisotropy (FA)) were used to probe rectal cancer stromal heterogeneity. FA provided the best discrimination between cancer and desmoplasia, fibrous tissue and muscularis propria. Cancer had relatively isotropic diffusion (mean FA 0.14), whereas desmoplasia (FA 0.31) and fibrous tissue (FA 0.34) had anisotropic diffusion with significantly higher FA than cancer (p < 0.001). Tumour was distinguished from muscularis propria (FA 0.61) which was highly anisotropic with higher FA than cancer (p < 0.001). This study showed that DTI-MRI can assist in more accurately defining tumour extent in rectal cancer. Nature Publishing Group UK 2019-06-27 /pmc/articles/PMC6597556/ /pubmed/31249325 http://dx.doi.org/10.1038/s41598-019-45450-2 Text en © The Author(s) 2019 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
Pham, Trang T.
Stait-Gardner, Timothy
Lee, Cheok Soon
Barton, Michael
Graham, Petra L.
Liney, Gary
Wong, Karen
Price, William S.
Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title_full Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title_fullStr Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title_full_unstemmed Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title_short Correlation of ultra-high field MRI with histopathology for evaluation of rectal cancer heterogeneity
title_sort correlation of ultra-high field mri with histopathology for evaluation of rectal cancer heterogeneity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6597556/
https://www.ncbi.nlm.nih.gov/pubmed/31249325
http://dx.doi.org/10.1038/s41598-019-45450-2
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