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The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy

BACKGROUND: To investigate the role of mpMRI and high PIRADS score as independent triggers in the qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy. METHODS: Between January 2017 and June 2019, 494 laparoscopic radical prostatectomies were performed in our inst...

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Autores principales: Nyk, Łukasz, Tayara, Omar, Ząbkowski, Tomasz, Kryst, Piotr, Andrychowicz, Aneta, Malewski, Wojciech
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130114/
https://www.ncbi.nlm.nih.gov/pubmed/34006281
http://dx.doi.org/10.1186/s12894-021-00850-3
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author Nyk, Łukasz
Tayara, Omar
Ząbkowski, Tomasz
Kryst, Piotr
Andrychowicz, Aneta
Malewski, Wojciech
author_facet Nyk, Łukasz
Tayara, Omar
Ząbkowski, Tomasz
Kryst, Piotr
Andrychowicz, Aneta
Malewski, Wojciech
author_sort Nyk, Łukasz
collection PubMed
description BACKGROUND: To investigate the role of mpMRI and high PIRADS score as independent triggers in the qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy. METHODS: Between January 2017 and June 2019, 494 laparoscopic radical prostatectomies were performed in our institution, including 203 patients (41.1%) with ISUP 1 cT1c-2c PCa on biopsy. Data regarding biopsy results, digital rectal examination, PSA, mpMRI and postoperative pathological report have been retrospectively analysed. RESULTS: In 183 cases (90.1%) mpMRI has been performed at least 6 weeks after biopsy. Final pathology revealed ISUP Gleason Grade Group upgrade in 62.6% of cases. PIRADS 5, PIRADS 4 and PIRADS 3 were associated with Gleason Grade Group upgrade in 70.5%, 62.8%, 48.3% of patients on final pathology, respectively. Within PIRADS 5 group, the number of upgraded cases was statistically significant. CONCLUSIONS: PIRADS score correlates with an upgrade on final pathology and may justify shared decision of radical treatment in patients unwilling to repeated biopsies. However, the use of PIRADS 5 score as a sole indicator for prostatectomy may result in nonnegligible overtreatment rate.
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spelling pubmed-81301142021-05-18 The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy Nyk, Łukasz Tayara, Omar Ząbkowski, Tomasz Kryst, Piotr Andrychowicz, Aneta Malewski, Wojciech BMC Urol Research Article BACKGROUND: To investigate the role of mpMRI and high PIRADS score as independent triggers in the qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy. METHODS: Between January 2017 and June 2019, 494 laparoscopic radical prostatectomies were performed in our institution, including 203 patients (41.1%) with ISUP 1 cT1c-2c PCa on biopsy. Data regarding biopsy results, digital rectal examination, PSA, mpMRI and postoperative pathological report have been retrospectively analysed. RESULTS: In 183 cases (90.1%) mpMRI has been performed at least 6 weeks after biopsy. Final pathology revealed ISUP Gleason Grade Group upgrade in 62.6% of cases. PIRADS 5, PIRADS 4 and PIRADS 3 were associated with Gleason Grade Group upgrade in 70.5%, 62.8%, 48.3% of patients on final pathology, respectively. Within PIRADS 5 group, the number of upgraded cases was statistically significant. CONCLUSIONS: PIRADS score correlates with an upgrade on final pathology and may justify shared decision of radical treatment in patients unwilling to repeated biopsies. However, the use of PIRADS 5 score as a sole indicator for prostatectomy may result in nonnegligible overtreatment rate. BioMed Central 2021-05-18 /pmc/articles/PMC8130114/ /pubmed/34006281 http://dx.doi.org/10.1186/s12894-021-00850-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Nyk, Łukasz
Tayara, Omar
Ząbkowski, Tomasz
Kryst, Piotr
Andrychowicz, Aneta
Malewski, Wojciech
The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title_full The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title_fullStr The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title_full_unstemmed The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title_short The role of mpMRI in qualification of patients with ISUP 1 prostate cancer on biopsy to radical prostatectomy
title_sort role of mpmri in qualification of patients with isup 1 prostate cancer on biopsy to radical prostatectomy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130114/
https://www.ncbi.nlm.nih.gov/pubmed/34006281
http://dx.doi.org/10.1186/s12894-021-00850-3
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