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Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer

OBJECTIVE: To assess the outcomes of pre‐biopsy magnetic resonance imaging (MRI) pathways, as a tool in biopsy‐naïve men with suspicion of prostate cancer, in routine clinical practice. Secondary outcomes included a comparison of transrectal MRI‐directed biopsy (TR‐MRDB) and transperineal (TP)‐MRDB...

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Autores principales: Israël, Bas, Immerzeel, Jos, van der Leest, Marloes, Hannink, Gerjon, Zámecnik, Patrik, Bomers, Joyce, Schoots, Ivo G., van Basten, Jean‐Paul, Debruyne, Frans, van Oort, Inge, Sedelaar, Michiel, Barentsz, Jelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291303/
https://www.ncbi.nlm.nih.gov/pubmed/34358388
http://dx.doi.org/10.1111/bju.15562
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author Israël, Bas
Immerzeel, Jos
van der Leest, Marloes
Hannink, Gerjon
Zámecnik, Patrik
Bomers, Joyce
Schoots, Ivo G.
van Basten, Jean‐Paul
Debruyne, Frans
van Oort, Inge
Sedelaar, Michiel
Barentsz, Jelle
author_facet Israël, Bas
Immerzeel, Jos
van der Leest, Marloes
Hannink, Gerjon
Zámecnik, Patrik
Bomers, Joyce
Schoots, Ivo G.
van Basten, Jean‐Paul
Debruyne, Frans
van Oort, Inge
Sedelaar, Michiel
Barentsz, Jelle
author_sort Israël, Bas
collection PubMed
description OBJECTIVE: To assess the outcomes of pre‐biopsy magnetic resonance imaging (MRI) pathways, as a tool in biopsy‐naïve men with suspicion of prostate cancer, in routine clinical practice. Secondary outcomes included a comparison of transrectal MRI‐directed biopsy (TR‐MRDB) and transperineal (TP)‐MRDB in men with suspicious MRI. PATIENTS AND METHODS: We retrospectively assessed a two‐centre cohort of consecutive biopsy‐naïve men with suspicion of prostate cancer who underwent a Prostate Imaging‐Reporting and Data System version 2 (PI‐RADS v2) compliant pre‐biopsy MRI in a single, high‐volume centre between 2015 and 2019 (Centre 1). Men with suspicious MRI scans underwent TR‐MRDB in Centre 1 and TP‐MRDB with additional random biopsies (RB) in Centre 2. The MRI and histopathology were assessed in the same institution (Centre 1). Outcomes included: (i) overall detection rates of Grade Group (GG) 1, GG ≥2, and GG ≥3 cancer in men with suspicious MRI; (ii) Biopsy‐avoidance due to non‐suspicious MRI; and (iii) Cancer detection rates and biopsy‐related complications between TR‐ and TP‐MRDB. To reduce confounding bias for MRDB comparisons, inverse probability weighting (IPW) was performed for age, digital rectal examination, prostate‐specific antigen (PSA), prostate volume, PSA density, and PI‐RADS category. RESULTS: Of the 2597 men included, the overall GG 1, GG ≥2, and GG ≥3 prevalence was 8% (210/2597), 27% (697/2597), and 15% (396/2597), respectively. Biopsy was avoided in 57% (1488/2597) of men. After IPW, the GG 1, GG ≥2 and GG ≥3 detection rates after TR‐ and TP‐MRDB were comparable at 24%, 57%, and 32%; and 18%, 64%, and 38%, respectively; with mean differences of −5.7% (95% confidence interval [CI] −13% to 1.4%), 6.1% (95% CI −2.1% to 14%), and 5.7% (95% CI −1.7% to 13%). Complications were similar in TR‐MRDB (0.50%) and TP‐MRDB with RB (0.62%; mean difference 0.11%, 95% CI −0.87% to 1.1%). CONCLUSION: This high‐volume, two‐centre study shows pre‐biopsy MRI as a decision tool is implementable in daily clinical practice. Compared to recent trials, a substantially higher biopsy avoidance rate was achieved without compromising GG ≥2/GG ≥3 detection and coinciding with lower over detection rates of GG 1 cancer. Prostate cancer detection and complication rates were comparable for TR‐ and TP‐MRDB.
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spelling pubmed-92913032022-07-20 Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer Israël, Bas Immerzeel, Jos van der Leest, Marloes Hannink, Gerjon Zámecnik, Patrik Bomers, Joyce Schoots, Ivo G. van Basten, Jean‐Paul Debruyne, Frans van Oort, Inge Sedelaar, Michiel Barentsz, Jelle BJU Int Original Articles OBJECTIVE: To assess the outcomes of pre‐biopsy magnetic resonance imaging (MRI) pathways, as a tool in biopsy‐naïve men with suspicion of prostate cancer, in routine clinical practice. Secondary outcomes included a comparison of transrectal MRI‐directed biopsy (TR‐MRDB) and transperineal (TP)‐MRDB in men with suspicious MRI. PATIENTS AND METHODS: We retrospectively assessed a two‐centre cohort of consecutive biopsy‐naïve men with suspicion of prostate cancer who underwent a Prostate Imaging‐Reporting and Data System version 2 (PI‐RADS v2) compliant pre‐biopsy MRI in a single, high‐volume centre between 2015 and 2019 (Centre 1). Men with suspicious MRI scans underwent TR‐MRDB in Centre 1 and TP‐MRDB with additional random biopsies (RB) in Centre 2. The MRI and histopathology were assessed in the same institution (Centre 1). Outcomes included: (i) overall detection rates of Grade Group (GG) 1, GG ≥2, and GG ≥3 cancer in men with suspicious MRI; (ii) Biopsy‐avoidance due to non‐suspicious MRI; and (iii) Cancer detection rates and biopsy‐related complications between TR‐ and TP‐MRDB. To reduce confounding bias for MRDB comparisons, inverse probability weighting (IPW) was performed for age, digital rectal examination, prostate‐specific antigen (PSA), prostate volume, PSA density, and PI‐RADS category. RESULTS: Of the 2597 men included, the overall GG 1, GG ≥2, and GG ≥3 prevalence was 8% (210/2597), 27% (697/2597), and 15% (396/2597), respectively. Biopsy was avoided in 57% (1488/2597) of men. After IPW, the GG 1, GG ≥2 and GG ≥3 detection rates after TR‐ and TP‐MRDB were comparable at 24%, 57%, and 32%; and 18%, 64%, and 38%, respectively; with mean differences of −5.7% (95% confidence interval [CI] −13% to 1.4%), 6.1% (95% CI −2.1% to 14%), and 5.7% (95% CI −1.7% to 13%). Complications were similar in TR‐MRDB (0.50%) and TP‐MRDB with RB (0.62%; mean difference 0.11%, 95% CI −0.87% to 1.1%). CONCLUSION: This high‐volume, two‐centre study shows pre‐biopsy MRI as a decision tool is implementable in daily clinical practice. Compared to recent trials, a substantially higher biopsy avoidance rate was achieved without compromising GG ≥2/GG ≥3 detection and coinciding with lower over detection rates of GG 1 cancer. Prostate cancer detection and complication rates were comparable for TR‐ and TP‐MRDB. John Wiley and Sons Inc. 2021-08-23 2022-04 /pmc/articles/PMC9291303/ /pubmed/34358388 http://dx.doi.org/10.1111/bju.15562 Text en © 2021 The Authors. BJU International published by John Wiley & Sons Ltd on behalf of BJU International. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Israël, Bas
Immerzeel, Jos
van der Leest, Marloes
Hannink, Gerjon
Zámecnik, Patrik
Bomers, Joyce
Schoots, Ivo G.
van Basten, Jean‐Paul
Debruyne, Frans
van Oort, Inge
Sedelaar, Michiel
Barentsz, Jelle
Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title_full Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title_fullStr Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title_full_unstemmed Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title_short Clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
title_sort clinical implementation of pre‐biopsy magnetic resonance imaging pathways for the diagnosis of prostate cancer
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291303/
https://www.ncbi.nlm.nih.gov/pubmed/34358388
http://dx.doi.org/10.1111/bju.15562
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