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Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis

Pre-biopsy multiparametric MRI is now recommended by multiple guidelines, not only for men with persistent suspicion of prostate cancer after prior negative systematic biopsy, but also at initial screening before the first biopsy. The major benefit of pre-biopsy MRI in the diagnostic work-up is to p...

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Autores principales: Schoots, Ivo G., Padhani, Anwar R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716818/
https://www.ncbi.nlm.nih.gov/pubmed/32356003
http://dx.doi.org/10.1007/s00261-020-02547-x
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author Schoots, Ivo G.
Padhani, Anwar R.
author_facet Schoots, Ivo G.
Padhani, Anwar R.
author_sort Schoots, Ivo G.
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description Pre-biopsy multiparametric MRI is now recommended by multiple guidelines, not only for men with persistent suspicion of prostate cancer after prior negative systematic biopsy, but also at initial screening before the first biopsy. The major benefit of pre-biopsy MRI in the diagnostic work-up is to promote individualized risk-adapted approaches for biopsy-decision management. Multiple MRI-directed diagnostic pathways can be conceived, with each approach having net-benefit trade-offs between benefits and harms, based on improved diagnostic yields of significant cancers and reduced biopsy testing and reduced detection of indolent prostate cancer. In this paper, we illustrate how clinical benefits can be maximized in men with MRI-negative and MRI-positive results, using the PI-RADS Multiparametric MRI and MRI-directed biopsy pathway. From a practice perspective, we emphasize five golden rules: (1) that multiparametric MRI approach including targeted biopsies be reserved for men likely to benefit from early detection and treatment of prostate cancer; (2) that there is a need to carefully assess risk of significant disease using PSA and clinical parameters before and after MRI; (3) do not offer immediate biopsy if the MRI is negative, unless other high-risk factors are present; (4) accept that not all significant cancers are found immediately and have robust ‘safety nets’ for men with negative MRI scans who avoid immediate biopsy and for positive MRI patients with negative or non-explanatory histology; and (5) use MRI-directed biopsy methods that minimize overdiagnosis and improve risk stratification.
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spelling pubmed-77168182020-12-04 Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis Schoots, Ivo G. Padhani, Anwar R. Abdom Radiol (NY) Special Section : Prostate cancer update Pre-biopsy multiparametric MRI is now recommended by multiple guidelines, not only for men with persistent suspicion of prostate cancer after prior negative systematic biopsy, but also at initial screening before the first biopsy. The major benefit of pre-biopsy MRI in the diagnostic work-up is to promote individualized risk-adapted approaches for biopsy-decision management. Multiple MRI-directed diagnostic pathways can be conceived, with each approach having net-benefit trade-offs between benefits and harms, based on improved diagnostic yields of significant cancers and reduced biopsy testing and reduced detection of indolent prostate cancer. In this paper, we illustrate how clinical benefits can be maximized in men with MRI-negative and MRI-positive results, using the PI-RADS Multiparametric MRI and MRI-directed biopsy pathway. From a practice perspective, we emphasize five golden rules: (1) that multiparametric MRI approach including targeted biopsies be reserved for men likely to benefit from early detection and treatment of prostate cancer; (2) that there is a need to carefully assess risk of significant disease using PSA and clinical parameters before and after MRI; (3) do not offer immediate biopsy if the MRI is negative, unless other high-risk factors are present; (4) accept that not all significant cancers are found immediately and have robust ‘safety nets’ for men with negative MRI scans who avoid immediate biopsy and for positive MRI patients with negative or non-explanatory histology; and (5) use MRI-directed biopsy methods that minimize overdiagnosis and improve risk stratification. Springer US 2020-04-30 2020 /pmc/articles/PMC7716818/ /pubmed/32356003 http://dx.doi.org/10.1007/s00261-020-02547-x Text en © The Author(s) 2020 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/.
spellingShingle Special Section : Prostate cancer update
Schoots, Ivo G.
Padhani, Anwar R.
Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title_full Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title_fullStr Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title_full_unstemmed Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title_short Delivering Clinical impacts of the MRI diagnostic pathway in prostate cancer diagnosis
title_sort delivering clinical impacts of the mri diagnostic pathway in prostate cancer diagnosis
topic Special Section : Prostate cancer update
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716818/
https://www.ncbi.nlm.nih.gov/pubmed/32356003
http://dx.doi.org/10.1007/s00261-020-02547-x
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