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Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers

Accurate staging of prostate cancer (PCa) at initial diagnosis and at biochemical recurrence is important to determine prognosis and the optimal treatment strategy. To date, treatment of metastatic PCa has mostly been based on the results of conventional imaging with abdominopelvic computed tomograp...

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Autores principales: Luining, Wietske I., Meijer, Dennie, Dahele, Max R., Vis, André N., Oprea-Lager, Daniela E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828280/
https://www.ncbi.nlm.nih.gov/pubmed/33450817
http://dx.doi.org/10.3390/diagnostics11010117
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author Luining, Wietske I.
Meijer, Dennie
Dahele, Max R.
Vis, André N.
Oprea-Lager, Daniela E.
author_facet Luining, Wietske I.
Meijer, Dennie
Dahele, Max R.
Vis, André N.
Oprea-Lager, Daniela E.
author_sort Luining, Wietske I.
collection PubMed
description Accurate staging of prostate cancer (PCa) at initial diagnosis and at biochemical recurrence is important to determine prognosis and the optimal treatment strategy. To date, treatment of metastatic PCa has mostly been based on the results of conventional imaging with abdominopelvic computed tomography (CT) and bone scintigraphy. However, these investigations have limited sensitivity and specificity which impairs their ability to accurately identify and quantify the true extent of active disease. Modern imaging modalities, such as those based on the detection of radioactively labeled tracers with combined positron emission tomography/computed tomography (PET/CT) scanning have been developed specifically for the detection of PCa. Novel radiotracers include (18)F-sodium fluoride (NaF), (11)C-/(18)F-fluorocholine (FCH), (18)F-fluordihydrotestosterone (FDHT), (68)Gallium and (18)F-radiolabeled prostate-specific membrane antigen (e.g., (68)Ga-PSMA-11, (18)F-DCFPyL). PET/CT with these tracers outperforms conventional imaging. As a result of this, although their impact on outcome needs to be better defined in appropriate clinical trials, techniques like prostate-specific membrane antigen (PSMA) PET/CT have been rapidly adopted into clinical practice for (re)staging PCa. This review focuses on nuclear imaging for PCa bone metastases, summarizing the literature on conventional imaging (focusing on CT and bone scintigraphy—magnetic resonance imaging is not addressed in this review), highlighting the prognostic importance of high and low volume metastatic disease which serves as a driver for the development of better imaging techniques, and finally discussing modern nuclear imaging with novel radiotracers.
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spelling pubmed-78282802021-01-25 Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers Luining, Wietske I. Meijer, Dennie Dahele, Max R. Vis, André N. Oprea-Lager, Daniela E. Diagnostics (Basel) Review Accurate staging of prostate cancer (PCa) at initial diagnosis and at biochemical recurrence is important to determine prognosis and the optimal treatment strategy. To date, treatment of metastatic PCa has mostly been based on the results of conventional imaging with abdominopelvic computed tomography (CT) and bone scintigraphy. However, these investigations have limited sensitivity and specificity which impairs their ability to accurately identify and quantify the true extent of active disease. Modern imaging modalities, such as those based on the detection of radioactively labeled tracers with combined positron emission tomography/computed tomography (PET/CT) scanning have been developed specifically for the detection of PCa. Novel radiotracers include (18)F-sodium fluoride (NaF), (11)C-/(18)F-fluorocholine (FCH), (18)F-fluordihydrotestosterone (FDHT), (68)Gallium and (18)F-radiolabeled prostate-specific membrane antigen (e.g., (68)Ga-PSMA-11, (18)F-DCFPyL). PET/CT with these tracers outperforms conventional imaging. As a result of this, although their impact on outcome needs to be better defined in appropriate clinical trials, techniques like prostate-specific membrane antigen (PSMA) PET/CT have been rapidly adopted into clinical practice for (re)staging PCa. This review focuses on nuclear imaging for PCa bone metastases, summarizing the literature on conventional imaging (focusing on CT and bone scintigraphy—magnetic resonance imaging is not addressed in this review), highlighting the prognostic importance of high and low volume metastatic disease which serves as a driver for the development of better imaging techniques, and finally discussing modern nuclear imaging with novel radiotracers. MDPI 2021-01-13 /pmc/articles/PMC7828280/ /pubmed/33450817 http://dx.doi.org/10.3390/diagnostics11010117 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Luining, Wietske I.
Meijer, Dennie
Dahele, Max R.
Vis, André N.
Oprea-Lager, Daniela E.
Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title_full Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title_fullStr Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title_full_unstemmed Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title_short Nuclear Imaging for Bone Metastases in Prostate Cancer: The Emergence of Modern Techniques Using Novel Radiotracers
title_sort nuclear imaging for bone metastases in prostate cancer: the emergence of modern techniques using novel radiotracers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7828280/
https://www.ncbi.nlm.nih.gov/pubmed/33450817
http://dx.doi.org/10.3390/diagnostics11010117
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