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A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging
Dynamic contrast-enhanced MR imaging (DCE-MRI) may act as a biomarker for successful cancer therapy. Simple, reproducible techniques may widen this application. This paper demonstrates a single slice imaging technique. The image acquisition is performed in less than 500 ms making it relatively insen...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361281/ https://www.ncbi.nlm.nih.gov/pubmed/16670720 http://dx.doi.org/10.1038/sj.bjc.6603140 |
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author | Morgan, B Utting, J F Higginson, A Thomas, A L Steward, W P Horsfield, M A |
author_facet | Morgan, B Utting, J F Higginson, A Thomas, A L Steward, W P Horsfield, M A |
author_sort | Morgan, B |
collection | PubMed |
description | Dynamic contrast-enhanced MR imaging (DCE-MRI) may act as a biomarker for successful cancer therapy. Simple, reproducible techniques may widen this application. This paper demonstrates a single slice imaging technique. The image acquisition is performed in less than 500 ms making it relatively insensitive to respiratory motion. Data from phantom studies and a reproducibility study in solid human tumours are presented. The reproducibility study showed a coefficient of variation (CoV) of 19.1% for K(trans) and 15.8% for the initial area under the contrast enhancement curve (IAUC). This was improved to 16 and 13.9% if tumours of diameter less than 3 cm were excluded. The individual repeatability (the range within which individual measurements are expected to fall) was 30.6% for K(trans) and 26.5% for IAUC for tumours greater than 3 cm diameter. This approach to DCE–MRI image acquisition can be performed with standard clinical scanners, and data analysis is straightforward. For treatment trials with 10 patients in a cohort, the CoV implies that the method would be sensitive to a treatment effect of greater than 18%. The individual repeatability is well inside the 40% change shown to be important in clinical studies using this DCE–MRI technique. |
format | Text |
id | pubmed-2361281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23612812009-09-10 A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging Morgan, B Utting, J F Higginson, A Thomas, A L Steward, W P Horsfield, M A Br J Cancer Clinical Study Dynamic contrast-enhanced MR imaging (DCE-MRI) may act as a biomarker for successful cancer therapy. Simple, reproducible techniques may widen this application. This paper demonstrates a single slice imaging technique. The image acquisition is performed in less than 500 ms making it relatively insensitive to respiratory motion. Data from phantom studies and a reproducibility study in solid human tumours are presented. The reproducibility study showed a coefficient of variation (CoV) of 19.1% for K(trans) and 15.8% for the initial area under the contrast enhancement curve (IAUC). This was improved to 16 and 13.9% if tumours of diameter less than 3 cm were excluded. The individual repeatability (the range within which individual measurements are expected to fall) was 30.6% for K(trans) and 26.5% for IAUC for tumours greater than 3 cm diameter. This approach to DCE–MRI image acquisition can be performed with standard clinical scanners, and data analysis is straightforward. For treatment trials with 10 patients in a cohort, the CoV implies that the method would be sensitive to a treatment effect of greater than 18%. The individual repeatability is well inside the 40% change shown to be important in clinical studies using this DCE–MRI technique. Nature Publishing Group 2006-05-22 2006-05-02 /pmc/articles/PMC2361281/ /pubmed/16670720 http://dx.doi.org/10.1038/sj.bjc.6603140 Text en Copyright © 2006 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Morgan, B Utting, J F Higginson, A Thomas, A L Steward, W P Horsfield, M A A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title | A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title_full | A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title_fullStr | A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title_full_unstemmed | A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title_short | A simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced MR imaging |
title_sort | simple, reproducible method for monitoring the treatment of tumours using dynamic contrast-enhanced mr imaging |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361281/ https://www.ncbi.nlm.nih.gov/pubmed/16670720 http://dx.doi.org/10.1038/sj.bjc.6603140 |
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