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Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -

PURPOSE: The detection of lymph-node metastases (N1) with conventional imaging such as magnetic resonance imaging (MRI) and computed tomography (CT) is inadequate for primarily diagnosed prostate cancer (PCa). Prostate-specific membrane antigen (PSMA) PET/CT is successfully introduced for the stagin...

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Autores principales: Jansen, B. H. E., Bodar, Y. J. L., Zwezerijnen, G. J. C., Meijer, D., van der Voorn, J. P., Nieuwenhuijzen, J. A., Wondergem, M., Roeleveld, T. A., Boellaard, R., Hoekstra, O. S., van Moorselaar, R. J. A., Oprea-Lager, D. E., Vis, A. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835187/
https://www.ncbi.nlm.nih.gov/pubmed/32789599
http://dx.doi.org/10.1007/s00259-020-04974-w
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author Jansen, B. H. E.
Bodar, Y. J. L.
Zwezerijnen, G. J. C.
Meijer, D.
van der Voorn, J. P.
Nieuwenhuijzen, J. A.
Wondergem, M.
Roeleveld, T. A.
Boellaard, R.
Hoekstra, O. S.
van Moorselaar, R. J. A.
Oprea-Lager, D. E.
Vis, A. N.
author_facet Jansen, B. H. E.
Bodar, Y. J. L.
Zwezerijnen, G. J. C.
Meijer, D.
van der Voorn, J. P.
Nieuwenhuijzen, J. A.
Wondergem, M.
Roeleveld, T. A.
Boellaard, R.
Hoekstra, O. S.
van Moorselaar, R. J. A.
Oprea-Lager, D. E.
Vis, A. N.
author_sort Jansen, B. H. E.
collection PubMed
description PURPOSE: The detection of lymph-node metastases (N1) with conventional imaging such as magnetic resonance imaging (MRI) and computed tomography (CT) is inadequate for primarily diagnosed prostate cancer (PCa). Prostate-specific membrane antigen (PSMA) PET/CT is successfully introduced for the staging of (biochemically) recurrent PCa. Besides the frequently used (68)gallium-labelled PSMA tracers, (18)fluorine-labelled PSMA tracers are available. This study examined the diagnostic accuracy of (18)F-DCFPyL (PSMA) PET/CT for lymph-node staging in primary PCa. METHODS: This was a prospective, multicentre cohort study. Patients with primary PCa underwent (18)F-DCFPyL PET/CT prior to robot-assisted radical prostatectomy (RARP) with extended pelvic lymph-node dissection (ePLND). Patients were included between October 2017 and January 2020. A Memorial Sloan Kettering Cancer Centre (MSKCC) nomogram risk probability of ≥ 8% of lymph-node metastases was set to perform ePLND. All images were reviewed by two experienced nuclear physicians, and were compared with post-operative histopathologic results. RESULTS: A total of 117 patients was analysed. Lymph-node metastases (N1) were histologically diagnosed in 17/117 patients (14.5%). The sensitivity, specificity, positive predictive value and negative predictive value for the (18)F-DCFPyL PET/CT detection of pelvic lymph-node metastases on a patient level were 41.2% (confidence interval (CI): 19.4–66.5%), 94.0% (CI 86.9–97.5%), 53.8% (CI 26.1–79.6%) and 90.4% (CI 82.6–95.0%), respectively. CONCLUSION: (18)F-DCFPyL PET/CT showed a high specificity (94.4%), yet a limited sensitivity (41.2%) for the detection of pelvic lymph-node metastases in primary PCa. This implies that current PSMA PET/CT imaging cannot replace diagnostic ePLND. Further research is necessary to define the exact place of PSMA PET/CT imaging in the primary staging of PCa.
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spelling pubmed-78351872021-01-29 Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial - Jansen, B. H. E. Bodar, Y. J. L. Zwezerijnen, G. J. C. Meijer, D. van der Voorn, J. P. Nieuwenhuijzen, J. A. Wondergem, M. Roeleveld, T. A. Boellaard, R. Hoekstra, O. S. van Moorselaar, R. J. A. Oprea-Lager, D. E. Vis, A. N. Eur J Nucl Med Mol Imaging Original Article PURPOSE: The detection of lymph-node metastases (N1) with conventional imaging such as magnetic resonance imaging (MRI) and computed tomography (CT) is inadequate for primarily diagnosed prostate cancer (PCa). Prostate-specific membrane antigen (PSMA) PET/CT is successfully introduced for the staging of (biochemically) recurrent PCa. Besides the frequently used (68)gallium-labelled PSMA tracers, (18)fluorine-labelled PSMA tracers are available. This study examined the diagnostic accuracy of (18)F-DCFPyL (PSMA) PET/CT for lymph-node staging in primary PCa. METHODS: This was a prospective, multicentre cohort study. Patients with primary PCa underwent (18)F-DCFPyL PET/CT prior to robot-assisted radical prostatectomy (RARP) with extended pelvic lymph-node dissection (ePLND). Patients were included between October 2017 and January 2020. A Memorial Sloan Kettering Cancer Centre (MSKCC) nomogram risk probability of ≥ 8% of lymph-node metastases was set to perform ePLND. All images were reviewed by two experienced nuclear physicians, and were compared with post-operative histopathologic results. RESULTS: A total of 117 patients was analysed. Lymph-node metastases (N1) were histologically diagnosed in 17/117 patients (14.5%). The sensitivity, specificity, positive predictive value and negative predictive value for the (18)F-DCFPyL PET/CT detection of pelvic lymph-node metastases on a patient level were 41.2% (confidence interval (CI): 19.4–66.5%), 94.0% (CI 86.9–97.5%), 53.8% (CI 26.1–79.6%) and 90.4% (CI 82.6–95.0%), respectively. CONCLUSION: (18)F-DCFPyL PET/CT showed a high specificity (94.4%), yet a limited sensitivity (41.2%) for the detection of pelvic lymph-node metastases in primary PCa. This implies that current PSMA PET/CT imaging cannot replace diagnostic ePLND. Further research is necessary to define the exact place of PSMA PET/CT imaging in the primary staging of PCa. Springer Berlin Heidelberg 2020-08-12 2021 /pmc/articles/PMC7835187/ /pubmed/32789599 http://dx.doi.org/10.1007/s00259-020-04974-w Text en © The Author(s) 2020 Open Access 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Original Article
Jansen, B. H. E.
Bodar, Y. J. L.
Zwezerijnen, G. J. C.
Meijer, D.
van der Voorn, J. P.
Nieuwenhuijzen, J. A.
Wondergem, M.
Roeleveld, T. A.
Boellaard, R.
Hoekstra, O. S.
van Moorselaar, R. J. A.
Oprea-Lager, D. E.
Vis, A. N.
Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title_full Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title_fullStr Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title_full_unstemmed Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title_short Pelvic lymph-node staging with (18)F-DCFPyL PET/CT prior to extended pelvic lymph-node dissection in primary prostate cancer - the SALT trial -
title_sort pelvic lymph-node staging with (18)f-dcfpyl pet/ct prior to extended pelvic lymph-node dissection in primary prostate cancer - the salt trial -
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835187/
https://www.ncbi.nlm.nih.gov/pubmed/32789599
http://dx.doi.org/10.1007/s00259-020-04974-w
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