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(18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging
Prostate-specific membrane antigen (PSMA)-targeted PET imaging for prostate cancer with (68)Ga-labeled compounds has rapidly become adopted as part of routine clinical care in many parts of the world. However, recent years have witnessed the start of a shift from (68)Ga- to (18)F-labeled PSMA-target...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929634/ https://www.ncbi.nlm.nih.gov/pubmed/31903102 http://dx.doi.org/10.7150/thno.37894 |
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author | Werner, Rudolf A. Derlin, Thorsten Lapa, Constantin Sheikbahaei, Sara Higuchi, Takahiro Giesel, Frederik L. Behr, Spencer Drzezga, Alexander Kimura, Hiroyuki Buck, Andreas K. Bengel, Frank M. Pomper, Martin G. Gorin, Michael A. Rowe, Steven P. |
author_facet | Werner, Rudolf A. Derlin, Thorsten Lapa, Constantin Sheikbahaei, Sara Higuchi, Takahiro Giesel, Frederik L. Behr, Spencer Drzezga, Alexander Kimura, Hiroyuki Buck, Andreas K. Bengel, Frank M. Pomper, Martin G. Gorin, Michael A. Rowe, Steven P. |
author_sort | Werner, Rudolf A. |
collection | PubMed |
description | Prostate-specific membrane antigen (PSMA)-targeted PET imaging for prostate cancer with (68)Ga-labeled compounds has rapidly become adopted as part of routine clinical care in many parts of the world. However, recent years have witnessed the start of a shift from (68)Ga- to (18)F-labeled PSMA-targeted compounds. The latter imaging agents have several key advantages, which may lay the groundwork for an even more widespread adoption into the clinic. First, facilitated delivery from distant suppliers expands the availability of PET radiopharmaceuticals in smaller hospitals operating a PET center but lacking the patient volume to justify an onsite (68)Ge/(68)Ga generator. Thus, such an approach meets the increasing demand for PSMA-targeted PET imaging in areas with lower population density and may even lead to cost-savings compared to in-house production. Moreover, (18)F-labeled radiotracers have a higher positron yield and lower positron energy, which in turn decreases image noise, improves contrast resolution, and maximizes the likelihood of detecting subtle lesions. In addition, the longer half-life of 110 min allows for improved delayed imaging protocols and flexibility in study design, which may further increase diagnostic accuracy. Moreover, such compounds can be distributed to sites which are not allowed to produce radiotracers on-site due to regulatory issues or to centers without access to a cyclotron. In light of these advantageous characteristics, (18)F-labeled PSMA-targeted PET radiotracers may play an important role in both optimizing this transformative imaging modality and making it widely available. We have aimed to provide a concise overview of emerging (18)F-labeled PSMA-targeted radiotracers undergoing active clinical development. Given the wide array of available radiotracers, comparative studies are needed to firmly establish the role of the available (18)F-labeled compounds in the field of molecular PCa imaging, preferably in different clinical scenarios. |
format | Online Article Text |
id | pubmed-6929634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-69296342020-01-04 (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging Werner, Rudolf A. Derlin, Thorsten Lapa, Constantin Sheikbahaei, Sara Higuchi, Takahiro Giesel, Frederik L. Behr, Spencer Drzezga, Alexander Kimura, Hiroyuki Buck, Andreas K. Bengel, Frank M. Pomper, Martin G. Gorin, Michael A. Rowe, Steven P. Theranostics Review Prostate-specific membrane antigen (PSMA)-targeted PET imaging for prostate cancer with (68)Ga-labeled compounds has rapidly become adopted as part of routine clinical care in many parts of the world. However, recent years have witnessed the start of a shift from (68)Ga- to (18)F-labeled PSMA-targeted compounds. The latter imaging agents have several key advantages, which may lay the groundwork for an even more widespread adoption into the clinic. First, facilitated delivery from distant suppliers expands the availability of PET radiopharmaceuticals in smaller hospitals operating a PET center but lacking the patient volume to justify an onsite (68)Ge/(68)Ga generator. Thus, such an approach meets the increasing demand for PSMA-targeted PET imaging in areas with lower population density and may even lead to cost-savings compared to in-house production. Moreover, (18)F-labeled radiotracers have a higher positron yield and lower positron energy, which in turn decreases image noise, improves contrast resolution, and maximizes the likelihood of detecting subtle lesions. In addition, the longer half-life of 110 min allows for improved delayed imaging protocols and flexibility in study design, which may further increase diagnostic accuracy. Moreover, such compounds can be distributed to sites which are not allowed to produce radiotracers on-site due to regulatory issues or to centers without access to a cyclotron. In light of these advantageous characteristics, (18)F-labeled PSMA-targeted PET radiotracers may play an important role in both optimizing this transformative imaging modality and making it widely available. We have aimed to provide a concise overview of emerging (18)F-labeled PSMA-targeted radiotracers undergoing active clinical development. Given the wide array of available radiotracers, comparative studies are needed to firmly establish the role of the available (18)F-labeled compounds in the field of molecular PCa imaging, preferably in different clinical scenarios. Ivyspring International Publisher 2020-01-01 /pmc/articles/PMC6929634/ /pubmed/31903102 http://dx.doi.org/10.7150/thno.37894 Text en © The author(s) This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Werner, Rudolf A. Derlin, Thorsten Lapa, Constantin Sheikbahaei, Sara Higuchi, Takahiro Giesel, Frederik L. Behr, Spencer Drzezga, Alexander Kimura, Hiroyuki Buck, Andreas K. Bengel, Frank M. Pomper, Martin G. Gorin, Michael A. Rowe, Steven P. (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title | (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title_full | (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title_fullStr | (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title_full_unstemmed | (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title_short | (18)F-Labeled, PSMA-Targeted Radiotracers: Leveraging the Advantages of Radiofluorination for Prostate Cancer Molecular Imaging |
title_sort | (18)f-labeled, psma-targeted radiotracers: leveraging the advantages of radiofluorination for prostate cancer molecular imaging |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6929634/ https://www.ncbi.nlm.nih.gov/pubmed/31903102 http://dx.doi.org/10.7150/thno.37894 |
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