Prostate Imaging Reporting and Data System Version 2.1: 2019 Update of Prostate Imaging Reporting and Data System Version 2

The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expecte...

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Published in:	European urology Vol. 76; no. 3; pp. 340 - 351
Main Authors:	Turkbey, Baris, Rosenkrantz, Andrew B., Haider, Masoom A., Padhani, Anwar R., Villeirs, Geert, Macura, Katarzyna J., Tempany, Clare M., Choyke, Peter L., Cornud, Francois, Margolis, Daniel J., Thoeny, Harriet C., Verma, Sadhna, Barentsz, Jelle, Weinreb, Jeffrey C.
Format:	Journal Article
Language:	English
Published:	Switzerland Elsevier B.V 01.09.2019
Subjects:	Consensus Data Systems Humans Image-Guided Biopsy - methods Magnetic Resonance Imaging - methods Male Prostate - diagnostic imaging Prostate cancer Prostate Imaging Reporting and Data System Version 2 Prostate Imaging Reporting and Data System Version 2.1 Prostatic Neoplasms - diagnosis Prostate Imaging Reporting and Data System Version 2 Prostate cancer Prostate Imaging Reporting and Data System Version 2.1
ISSN:	0302-2838, 1873-7560, 1873-7560
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Abstract	The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expected, have also identified a number of ambiguities and limitations, some of which have been documented in the literature with potential solutions offered. To address these issues, the PI-RADS Steering Committee, again using a consensus-based process, has recommended several modifications to PI-RADS v2, maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. This updated version, described in this article, is termed PI-RADS v2.1. It is anticipated that the adoption of these PI-RADS v2.1 modifications will improve inter-reader variability and simplify PI-RADS assessment of prostate magnetic resonance imaging even further. Research on the value and limitations on all components of PI-RADS v2.1 is strongly encouraged. The Prostate Imaging Reporting and Data System (PI-RADS) Committee, using a consensus-based process, has recommended several modifications to PI-RADS version 2 (v2), maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. The updated version is termed PI-RADS v2.1.
AbstractList	The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expected, have also identified a number of ambiguities and limitations, some of which have been documented in the literature with potential solutions offered. To address these issues, the PI-RADS Steering Committee, again using a consensus-based process, has recommended several modifications to PI-RADS v2, maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. This updated version, described in this article, is termed PI-RADS v2.1. It is anticipated that the adoption of these PI-RADS v2.1 modifications will improve inter-reader variability and simplify PI-RADS assessment of prostate magnetic resonance imaging even further. Research on the value and limitations on all components of PI-RADS v2.1 is strongly encouraged. The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expected, have also identified a number of ambiguities and limitations, some of which have been documented in the literature with potential solutions offered. To address these issues, the PI-RADS Steering Committee, again using a consensus-based process, has recommended several modifications to PI-RADS v2, maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. This updated version, described in this article, is termed PI-RADS v2.1. It is anticipated that the adoption of these PI-RADS v2.1 modifications will improve inter-reader variability and simplify PI-RADS assessment of prostate magnetic resonance imaging even further. Research on the value and limitations on all components of PI-RADS v2.1 is strongly encouraged.The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expected, have also identified a number of ambiguities and limitations, some of which have been documented in the literature with potential solutions offered. To address these issues, the PI-RADS Steering Committee, again using a consensus-based process, has recommended several modifications to PI-RADS v2, maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. This updated version, described in this article, is termed PI-RADS v2.1. It is anticipated that the adoption of these PI-RADS v2.1 modifications will improve inter-reader variability and simplify PI-RADS assessment of prostate magnetic resonance imaging even further. Research on the value and limitations on all components of PI-RADS v2.1 is strongly encouraged. The Prostate Imaging Reporting and Data System version 2 (PI-RADS v2) was developed with a consensus-based process using a combination of published data, and expert observations and opinions. In the short time since its release, numerous studies have validated the value of PI-RADS v2 but, as expected, have also identified a number of ambiguities and limitations, some of which have been documented in the literature with potential solutions offered. To address these issues, the PI-RADS Steering Committee, again using a consensus-based process, has recommended several modifications to PI-RADS v2, maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. This updated version, described in this article, is termed PI-RADS v2.1. It is anticipated that the adoption of these PI-RADS v2.1 modifications will improve inter-reader variability and simplify PI-RADS assessment of prostate magnetic resonance imaging even further. Research on the value and limitations on all components of PI-RADS v2.1 is strongly encouraged. The Prostate Imaging Reporting and Data System (PI-RADS) Committee, using a consensus-based process, has recommended several modifications to PI-RADS version 2 (v2), maintaining the framework of assigning scores to individual sequences and using these scores to derive an overall assessment category. The updated version is termed PI-RADS v2.1.
Author	Barentsz, Jelle Padhani, Anwar R. Thoeny, Harriet C. Haider, Masoom A. Tempany, Clare M. Choyke, Peter L. Turkbey, Baris Macura, Katarzyna J. Margolis, Daniel J. Cornud, Francois Villeirs, Geert Verma, Sadhna Rosenkrantz, Andrew B. Weinreb, Jeffrey C.
Author_xml	– sequence: 1 givenname: Baris surname: Turkbey fullname: Turkbey, Baris email: turkbeyi@mail.nih.gov organization: Molecular Imaging Program, National Cancer Institute, NIH, Bethesda, MD, USA – sequence: 2 givenname: Andrew B. surname: Rosenkrantz fullname: Rosenkrantz, Andrew B. email: Andrew.Rosenkrantz@nyulangone.org organization: Department of Radiology, NYU Langone Medical Center, New York, NY, USA – sequence: 3 givenname: Masoom A. surname: Haider fullname: Haider, Masoom A. organization: University of Toronto, Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Canada – sequence: 4 givenname: Anwar R. surname: Padhani fullname: Padhani, Anwar R. organization: Paul Strickland Scanner Centre, Mount Vernon Cancer Centre, Northwood, UK – sequence: 5 givenname: Geert surname: Villeirs fullname: Villeirs, Geert organization: Department of Radiology, Ghent University Hospital, Gent, Belgium – sequence: 6 givenname: Katarzyna J. surname: Macura fullname: Macura, Katarzyna J. organization: Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, USA – sequence: 7 givenname: Clare M. surname: Tempany fullname: Tempany, Clare M. organization: Department of Radiology, Brigham and Women's Hospital, Boston, MA, USA – sequence: 8 givenname: Peter L. surname: Choyke fullname: Choyke, Peter L. organization: Molecular Imaging Program, National Cancer Institute, NIH, Bethesda, MD, USA – sequence: 9 givenname: Francois surname: Cornud fullname: Cornud, Francois organization: Department of Radiology, Hôpital Cochin, Université Paris Descartes, Paris, France – sequence: 10 givenname: Daniel J. surname: Margolis fullname: Margolis, Daniel J. organization: Weill Cornell Imaging, Cornell University, New York, NY, USA – sequence: 11 givenname: Harriet C. surname: Thoeny fullname: Thoeny, Harriet C. organization: Department of Radiology, Hôpital Cantonal de Fribourg HFR, University of Fribourg, Fribourg, Switzerland – sequence: 12 givenname: Sadhna surname: Verma fullname: Verma, Sadhna organization: Department of Radiology, University of Cincinnati, College of Medicine, Cincinnati, OH, USA – sequence: 13 givenname: Jelle surname: Barentsz fullname: Barentsz, Jelle organization: Department of Radiology and Nuclear Medicine Radboudumc, Nijmegen, The Netherlands – sequence: 14 givenname: Jeffrey C. surname: Weinreb fullname: Weinreb, Jeffrey C. organization: Department of Radiology, Yale School of Medicine, New Haven, CT, USA
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SubjectTerms	Consensus Data Systems Humans Image-Guided Biopsy - methods Magnetic Resonance Imaging - methods Male Prostate - diagnostic imaging Prostate cancer Prostate Imaging Reporting and Data System Version 2 Prostate Imaging Reporting and Data System Version 2.1 Prostatic Neoplasms - diagnosis
Title	Prostate Imaging Reporting and Data System Version 2.1: 2019 Update of Prostate Imaging Reporting and Data System Version 2
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