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Contrast-enhanced ultrasound for examining tumor biology

This paper reviews the potential of ultrasound for assessing the viability and biological behavior of tumors. Unlike color Doppler sonography, modern techniques for contrast-enhanced ultrasound permit the measurement of tissue perfusion irrespective of vessel size or flow velocity. Perfusion can als...

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Detalles Bibliográficos
Autores principales: Delorme, Stefan, Krix, Martin
Formato: Texto
Lenguaje:English
Publicado: e-MED 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693765/
https://www.ncbi.nlm.nih.gov/pubmed/17015239
http://dx.doi.org/10.1102/1470-7330.2006.0023
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author Delorme, Stefan
Krix, Martin
author_facet Delorme, Stefan
Krix, Martin
author_sort Delorme, Stefan
collection PubMed
description This paper reviews the potential of ultrasound for assessing the viability and biological behavior of tumors. Unlike color Doppler sonography, modern techniques for contrast-enhanced ultrasound permit the measurement of tissue perfusion irrespective of vessel size or flow velocity. Perfusion can also be assessed quantitatively, using replenishment kinetics or derivates thereof. The perfusion of tumors is a surrogate parameter of their viability and may mirror their response to therapy. Furthermore, the degree of vascularity in a tumor may express its aggressiveness and help to predict its response to treatment. In animal models, a decrease in blood flow has been shown to precede a shrinkage of tumors treated with anti-angiogenic compounds. In liver metastases, arterial and portal blood supply can be assessed separately, and a response to stereotactic radiotherapy was found to go along with a decrease in arterial perfusion. Moreover, a relatively high arterial perfusion of liver metastases may predict a response to chemotherapy. Contrast-enhanced ultrasound may be a potent tool for assessing the effects of anti-angiogenic treatment in patients.
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spelling pubmed-16937652008-09-27 Contrast-enhanced ultrasound for examining tumor biology Delorme, Stefan Krix, Martin Cancer Imaging Article This paper reviews the potential of ultrasound for assessing the viability and biological behavior of tumors. Unlike color Doppler sonography, modern techniques for contrast-enhanced ultrasound permit the measurement of tissue perfusion irrespective of vessel size or flow velocity. Perfusion can also be assessed quantitatively, using replenishment kinetics or derivates thereof. The perfusion of tumors is a surrogate parameter of their viability and may mirror their response to therapy. Furthermore, the degree of vascularity in a tumor may express its aggressiveness and help to predict its response to treatment. In animal models, a decrease in blood flow has been shown to precede a shrinkage of tumors treated with anti-angiogenic compounds. In liver metastases, arterial and portal blood supply can be assessed separately, and a response to stereotactic radiotherapy was found to go along with a decrease in arterial perfusion. Moreover, a relatively high arterial perfusion of liver metastases may predict a response to chemotherapy. Contrast-enhanced ultrasound may be a potent tool for assessing the effects of anti-angiogenic treatment in patients. e-MED 2006-09-27 /pmc/articles/PMC1693765/ /pubmed/17015239 http://dx.doi.org/10.1102/1470-7330.2006.0023 Text en Copyright © 2006 International Cancer Imaging Society
spellingShingle Article
Delorme, Stefan
Krix, Martin
Contrast-enhanced ultrasound for examining tumor biology
title Contrast-enhanced ultrasound for examining tumor biology
title_full Contrast-enhanced ultrasound for examining tumor biology
title_fullStr Contrast-enhanced ultrasound for examining tumor biology
title_full_unstemmed Contrast-enhanced ultrasound for examining tumor biology
title_short Contrast-enhanced ultrasound for examining tumor biology
title_sort contrast-enhanced ultrasound for examining tumor biology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1693765/
https://www.ncbi.nlm.nih.gov/pubmed/17015239
http://dx.doi.org/10.1102/1470-7330.2006.0023
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