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Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET
OBJECTIVE: PET/CT and multiparametric MRI (mpMRI) are important diagnostic tools in clinically significant prostate cancer (csPC). The aim of this study was to compare csPC detection rates with [(68)Ga]PSMA-11-PET (PSMA)-PET, [(11)C]Acetate (ACE)-PET, and mpMRI with histopathology as reference, to i...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566593/ https://www.ncbi.nlm.nih.gov/pubmed/37615497 http://dx.doi.org/10.1097/MNM.0000000000001743 |
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author | Sandgren, Kristina Strandberg, Sara N. Jonsson, Joakim H. Grefve, Josefine Keeratijarut Lindberg, Angsana Nilsson, Erik Bergh, Anders Söderkvist, Karin Thellenberg Karlsson, Camilla Friedrich, Bengt Widmark, Anders Blomqvist, Lennart Berg Loegager, Vibeke Axelsson, Jan Ögren, Mattias Ögren, Margareta Nyholm, Tufve Riklund, Katrine |
author_facet | Sandgren, Kristina Strandberg, Sara N. Jonsson, Joakim H. Grefve, Josefine Keeratijarut Lindberg, Angsana Nilsson, Erik Bergh, Anders Söderkvist, Karin Thellenberg Karlsson, Camilla Friedrich, Bengt Widmark, Anders Blomqvist, Lennart Berg Loegager, Vibeke Axelsson, Jan Ögren, Mattias Ögren, Margareta Nyholm, Tufve Riklund, Katrine |
author_sort | Sandgren, Kristina |
collection | PubMed |
description | OBJECTIVE: PET/CT and multiparametric MRI (mpMRI) are important diagnostic tools in clinically significant prostate cancer (csPC). The aim of this study was to compare csPC detection rates with [(68)Ga]PSMA-11-PET (PSMA)-PET, [(11)C]Acetate (ACE)-PET, and mpMRI with histopathology as reference, to identify the most suitable imaging modalities for subsequent hybrid imaging. An additional aim was to compare inter-reader variability to assess reproducibility. METHODS: During 2016–2019, all study participants were examined with PSMA-PET/mpMRI and ACE-PET/CT prior to radical prostatectomy. PSMA-PET, ACE-PET and mpMRI were evaluated separately by two observers, and were compared with histopathology-defined csPC. Statistical analyses included two-sided McNemar test and index of specific agreement. RESULTS: Fifty-five study participants were included, with 130 histopathological intraprostatic lesions >0.05 cc. Of these, 32% (42/130) were classified as csPC with ISUP grade ≥2 and volume >0.5 cc. PSMA-PET and mpMRI showed no difference in performance (P = 0.48), with mean csPC detection rate of 70% (29.5/42) and 74% (31/42), respectively, while with ACE-PET the mean csPC detection rate was 37% (15.5/42). Interobserver agreement was higher with PSMA-PET compared to mpMRI [79% (26/33) vs 67% (24/38)]. Including all detected lesions from each pair of observers, the detection rate increased to 90% (38/42) with mpMRI, and 79% (33/42) with PSMA-PET. CONCLUSION: PSMA-PET and mpMRI showed high csPC detection rates and superior performance compared to ACE-PET. The interobserver agreement indicates higher reproducibility with PSMA-PET. The combined result of all observers in both PSMA-PET and mpMRI showed the highest detection rate, suggesting an added value of a hybrid imaging approach. |
format | Online Article Text |
id | pubmed-10566593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-105665932023-10-12 Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET Sandgren, Kristina Strandberg, Sara N. Jonsson, Joakim H. Grefve, Josefine Keeratijarut Lindberg, Angsana Nilsson, Erik Bergh, Anders Söderkvist, Karin Thellenberg Karlsson, Camilla Friedrich, Bengt Widmark, Anders Blomqvist, Lennart Berg Loegager, Vibeke Axelsson, Jan Ögren, Mattias Ögren, Margareta Nyholm, Tufve Riklund, Katrine Nucl Med Commun Original Articles OBJECTIVE: PET/CT and multiparametric MRI (mpMRI) are important diagnostic tools in clinically significant prostate cancer (csPC). The aim of this study was to compare csPC detection rates with [(68)Ga]PSMA-11-PET (PSMA)-PET, [(11)C]Acetate (ACE)-PET, and mpMRI with histopathology as reference, to identify the most suitable imaging modalities for subsequent hybrid imaging. An additional aim was to compare inter-reader variability to assess reproducibility. METHODS: During 2016–2019, all study participants were examined with PSMA-PET/mpMRI and ACE-PET/CT prior to radical prostatectomy. PSMA-PET, ACE-PET and mpMRI were evaluated separately by two observers, and were compared with histopathology-defined csPC. Statistical analyses included two-sided McNemar test and index of specific agreement. RESULTS: Fifty-five study participants were included, with 130 histopathological intraprostatic lesions >0.05 cc. Of these, 32% (42/130) were classified as csPC with ISUP grade ≥2 and volume >0.5 cc. PSMA-PET and mpMRI showed no difference in performance (P = 0.48), with mean csPC detection rate of 70% (29.5/42) and 74% (31/42), respectively, while with ACE-PET the mean csPC detection rate was 37% (15.5/42). Interobserver agreement was higher with PSMA-PET compared to mpMRI [79% (26/33) vs 67% (24/38)]. Including all detected lesions from each pair of observers, the detection rate increased to 90% (38/42) with mpMRI, and 79% (33/42) with PSMA-PET. CONCLUSION: PSMA-PET and mpMRI showed high csPC detection rates and superior performance compared to ACE-PET. The interobserver agreement indicates higher reproducibility with PSMA-PET. The combined result of all observers in both PSMA-PET and mpMRI showed the highest detection rate, suggesting an added value of a hybrid imaging approach. Lippincott Williams & Wilkins 2023-11 2023-08-24 /pmc/articles/PMC10566593/ /pubmed/37615497 http://dx.doi.org/10.1097/MNM.0000000000001743 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Original Articles Sandgren, Kristina Strandberg, Sara N. Jonsson, Joakim H. Grefve, Josefine Keeratijarut Lindberg, Angsana Nilsson, Erik Bergh, Anders Söderkvist, Karin Thellenberg Karlsson, Camilla Friedrich, Bengt Widmark, Anders Blomqvist, Lennart Berg Loegager, Vibeke Axelsson, Jan Ögren, Mattias Ögren, Margareta Nyholm, Tufve Riklund, Katrine Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title | Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title_full | Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title_fullStr | Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title_full_unstemmed | Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title_short | Histopathology-validated lesion detection rates of clinically significant prostate cancer with mpMRI, [(68)Ga]PSMA-11-PET and [(11)C]Acetate-PET |
title_sort | histopathology-validated lesion detection rates of clinically significant prostate cancer with mpmri, [(68)ga]psma-11-pet and [(11)c]acetate-pet |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10566593/ https://www.ncbi.nlm.nih.gov/pubmed/37615497 http://dx.doi.org/10.1097/MNM.0000000000001743 |
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