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F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients
PURPOSE: The prostate-specific membrane antigen (PSMA) targeted positron-emitting-tomography (PET) tracer (68)Ga-PSMA-11 shows great promise in the detection of prostate cancer. However, (68)Ga has several shortcomings as a radiolabel including short half-life and non-ideal energies, and this has mo...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323462/ https://www.ncbi.nlm.nih.gov/pubmed/27889802 http://dx.doi.org/10.1007/s00259-016-3573-4 |
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author | Giesel, Frederik L. Hadaschik, B. Cardinale, J. Radtke, J. Vinsensia, M. Lehnert, W. Kesch, C. Tolstov, Y. Singer, S. Grabe, N. Duensing, S. Schäfer, M. Neels, O. C. Mier, W. Haberkorn, U. Kopka, K. Kratochwil, C. |
author_facet | Giesel, Frederik L. Hadaschik, B. Cardinale, J. Radtke, J. Vinsensia, M. Lehnert, W. Kesch, C. Tolstov, Y. Singer, S. Grabe, N. Duensing, S. Schäfer, M. Neels, O. C. Mier, W. Haberkorn, U. Kopka, K. Kratochwil, C. |
author_sort | Giesel, Frederik L. |
collection | PubMed |
description | PURPOSE: The prostate-specific membrane antigen (PSMA) targeted positron-emitting-tomography (PET) tracer (68)Ga-PSMA-11 shows great promise in the detection of prostate cancer. However, (68)Ga has several shortcomings as a radiolabel including short half-life and non-ideal energies, and this has motivated consideration of (18)F-labelled analogs. (18)F-PSMA-1007 was selected among several (18)F-PSMA-ligand candidate compounds because it demonstrated high labelling yields, outstanding tumor uptake and fast, non-urinary background clearance. Here, we describe the properties of (18)F-PSMA-1007 in human volunteers and patients. METHODS: Radiation dosimetry of (18)F-PSMA-1007 was determined in three healthy volunteers who underwent whole-body PET-scans and concomitant blood and urine sampling. Following this, ten patients with high-risk prostate cancer underwent (18)F-PSMA-1007 PET/CT (1 h and 3 h p.i.) and normal organ biodistribution and tumor uptakes were examined. Eight patients underwent prostatectomy with extended pelvic lymphadenectomy. Uptake in intra-prostatic lesions and lymph node metastases were correlated with final histopathology, including PSMA immunostaining. RESULTS: With an effective dose of approximately 4.4–5.5 mSv per 200–250 MBq examination, (18)F-PSMA-1007 behaves similar to other PSMA-PET agents as well as to other (18)F-labelled PET-tracers. In comparison to other PSMA-targeting PET-tracers, (18)F-PSMA-1007 has reduced urinary clearance enabling excellent assessment of the prostate. Similar to (18)F-DCFPyL and with slightly slower clearance kinetics than PSMA-11, favorable tumor-to-background ratios are observed 2–3 h after injection. In eight patients, diagnostic findings were successfully validated by histopathology. (18)F-PSMA-1007 PET/CT detected 18 of 19 lymph node metastases in the pelvis, including nodes as small as 1 mm in diameter. CONCLUSION: (18)F-PSMA-1007 performs at least comparably to (68)Ga-PSMA-11, but its longer half-life combined with its superior energy characteristics and non-urinary excretion overcomes some practical limitations of (68)Ga-labelled PSMA-targeted tracers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00259-016-3573-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5323462 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53234622017-03-09 F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients Giesel, Frederik L. Hadaschik, B. Cardinale, J. Radtke, J. Vinsensia, M. Lehnert, W. Kesch, C. Tolstov, Y. Singer, S. Grabe, N. Duensing, S. Schäfer, M. Neels, O. C. Mier, W. Haberkorn, U. Kopka, K. Kratochwil, C. Eur J Nucl Med Mol Imaging Original Article PURPOSE: The prostate-specific membrane antigen (PSMA) targeted positron-emitting-tomography (PET) tracer (68)Ga-PSMA-11 shows great promise in the detection of prostate cancer. However, (68)Ga has several shortcomings as a radiolabel including short half-life and non-ideal energies, and this has motivated consideration of (18)F-labelled analogs. (18)F-PSMA-1007 was selected among several (18)F-PSMA-ligand candidate compounds because it demonstrated high labelling yields, outstanding tumor uptake and fast, non-urinary background clearance. Here, we describe the properties of (18)F-PSMA-1007 in human volunteers and patients. METHODS: Radiation dosimetry of (18)F-PSMA-1007 was determined in three healthy volunteers who underwent whole-body PET-scans and concomitant blood and urine sampling. Following this, ten patients with high-risk prostate cancer underwent (18)F-PSMA-1007 PET/CT (1 h and 3 h p.i.) and normal organ biodistribution and tumor uptakes were examined. Eight patients underwent prostatectomy with extended pelvic lymphadenectomy. Uptake in intra-prostatic lesions and lymph node metastases were correlated with final histopathology, including PSMA immunostaining. RESULTS: With an effective dose of approximately 4.4–5.5 mSv per 200–250 MBq examination, (18)F-PSMA-1007 behaves similar to other PSMA-PET agents as well as to other (18)F-labelled PET-tracers. In comparison to other PSMA-targeting PET-tracers, (18)F-PSMA-1007 has reduced urinary clearance enabling excellent assessment of the prostate. Similar to (18)F-DCFPyL and with slightly slower clearance kinetics than PSMA-11, favorable tumor-to-background ratios are observed 2–3 h after injection. In eight patients, diagnostic findings were successfully validated by histopathology. (18)F-PSMA-1007 PET/CT detected 18 of 19 lymph node metastases in the pelvis, including nodes as small as 1 mm in diameter. CONCLUSION: (18)F-PSMA-1007 performs at least comparably to (68)Ga-PSMA-11, but its longer half-life combined with its superior energy characteristics and non-urinary excretion overcomes some practical limitations of (68)Ga-labelled PSMA-targeted tracers. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00259-016-3573-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-11-26 2017 /pmc/articles/PMC5323462/ /pubmed/27889802 http://dx.doi.org/10.1007/s00259-016-3573-4 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Giesel, Frederik L. Hadaschik, B. Cardinale, J. Radtke, J. Vinsensia, M. Lehnert, W. Kesch, C. Tolstov, Y. Singer, S. Grabe, N. Duensing, S. Schäfer, M. Neels, O. C. Mier, W. Haberkorn, U. Kopka, K. Kratochwil, C. F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title | F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title_full | F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title_fullStr | F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title_full_unstemmed | F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title_short | F-18 labelled PSMA-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
title_sort | f-18 labelled psma-1007: biodistribution, radiation dosimetry and histopathological validation of tumor lesions in prostate cancer patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5323462/ https://www.ncbi.nlm.nih.gov/pubmed/27889802 http://dx.doi.org/10.1007/s00259-016-3573-4 |
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