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Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology

Background and objectives: Systematic prostate biopsy (SB) has a low Gleason group (GG) accuracy when compared to final pathology. This may negatively impact the inclusion of patients into specific risk groups and treatment choice. The aim of our study was to assess the GG accuracy of magnetic reson...

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Autores principales: Andras, Iulia, Cata, Emanuel Darius, Serban, Andreea, Kadula, Pierre, Telecan, Teodora, Buzoianu, Maximilian, Bungardean, Maria, Stanca, Dan Vasile, Coman, Ioan, Crisan, Nicolae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224801/
https://www.ncbi.nlm.nih.gov/pubmed/34067302
http://dx.doi.org/10.3390/medicina57060519
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author Andras, Iulia
Cata, Emanuel Darius
Serban, Andreea
Kadula, Pierre
Telecan, Teodora
Buzoianu, Maximilian
Bungardean, Maria
Stanca, Dan Vasile
Coman, Ioan
Crisan, Nicolae
author_facet Andras, Iulia
Cata, Emanuel Darius
Serban, Andreea
Kadula, Pierre
Telecan, Teodora
Buzoianu, Maximilian
Bungardean, Maria
Stanca, Dan Vasile
Coman, Ioan
Crisan, Nicolae
author_sort Andras, Iulia
collection PubMed
description Background and objectives: Systematic prostate biopsy (SB) has a low Gleason group (GG) accuracy when compared to final pathology. This may negatively impact the inclusion of patients into specific risk groups and treatment choice. The aim of our study was to assess the GG accuracy of magnetic resonance imaging-ultrasound (MRI-US) fusion prostate biopsy. Materials and Methods: Of a cohort of minimally invasive radical prostatectomy (RP), we selected all patients who were diagnosed with prostate cancer (PCa) via MRI-US fusion biopsy (n = 115). Results: Combined biopsy had the highest rate for GG concordance (61.7% vs. 60.4% for SB vs. 45.3% for MRI-US fusion biopsy) and the lowest for upgrading (20.9% vs. 24.5% for SB vs. 34.9% for MRI-US fusion biopsy), p < 0.0001. No clinical data were predictive for upgrading or downgrading at final pathology. Locally advanced PCa was associated with a high Prostate Imaging-Reporting and Data System (PIRADS) score (p = 0.0014) and higher percentages of positive biopsy cores (PBC)/targeted (p = 0.0002) and PBC/total (p = 0.01). Positive surgical margins were correlated with higher percentages of PBC/systematic (p = 0.003) and PBC/total (p = 0.009). Conclusions: Pre-biopsy prostate MRI improves GG concordance between biopsy and RP. Combined biopsy provides the highest grading accuracy when compared to final pathology. Targeted and systematic biopsy data are predictive for adverse pathologic outcomes.
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spelling pubmed-82248012021-06-25 Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology Andras, Iulia Cata, Emanuel Darius Serban, Andreea Kadula, Pierre Telecan, Teodora Buzoianu, Maximilian Bungardean, Maria Stanca, Dan Vasile Coman, Ioan Crisan, Nicolae Medicina (Kaunas) Article Background and objectives: Systematic prostate biopsy (SB) has a low Gleason group (GG) accuracy when compared to final pathology. This may negatively impact the inclusion of patients into specific risk groups and treatment choice. The aim of our study was to assess the GG accuracy of magnetic resonance imaging-ultrasound (MRI-US) fusion prostate biopsy. Materials and Methods: Of a cohort of minimally invasive radical prostatectomy (RP), we selected all patients who were diagnosed with prostate cancer (PCa) via MRI-US fusion biopsy (n = 115). Results: Combined biopsy had the highest rate for GG concordance (61.7% vs. 60.4% for SB vs. 45.3% for MRI-US fusion biopsy) and the lowest for upgrading (20.9% vs. 24.5% for SB vs. 34.9% for MRI-US fusion biopsy), p < 0.0001. No clinical data were predictive for upgrading or downgrading at final pathology. Locally advanced PCa was associated with a high Prostate Imaging-Reporting and Data System (PIRADS) score (p = 0.0014) and higher percentages of positive biopsy cores (PBC)/targeted (p = 0.0002) and PBC/total (p = 0.01). Positive surgical margins were correlated with higher percentages of PBC/systematic (p = 0.003) and PBC/total (p = 0.009). Conclusions: Pre-biopsy prostate MRI improves GG concordance between biopsy and RP. Combined biopsy provides the highest grading accuracy when compared to final pathology. Targeted and systematic biopsy data are predictive for adverse pathologic outcomes. MDPI 2021-05-22 /pmc/articles/PMC8224801/ /pubmed/34067302 http://dx.doi.org/10.3390/medicina57060519 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Andras, Iulia
Cata, Emanuel Darius
Serban, Andreea
Kadula, Pierre
Telecan, Teodora
Buzoianu, Maximilian
Bungardean, Maria
Stanca, Dan Vasile
Coman, Ioan
Crisan, Nicolae
Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title_full Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title_fullStr Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title_full_unstemmed Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title_short Combined Systematic and MRI-US Fusion Prostate Biopsy Has the Highest Grading Accuracy When Compared to Final Pathology
title_sort combined systematic and mri-us fusion prostate biopsy has the highest grading accuracy when compared to final pathology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8224801/
https://www.ncbi.nlm.nih.gov/pubmed/34067302
http://dx.doi.org/10.3390/medicina57060519
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