Background and objective: The Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations standardise the reporting of prostate magnetic resonance imaging (MRI) in patients on active surveillance (AS) for prostate cancer. An international consensus group recently updated these recommendations and identified the areas of uncertainty. Methods: A panel of 38 experts used the formal RAND/UCLA Appropriateness Method consensus methodology. Panellists scored 193 statements using a 1-9 agreement scale, where 9 means full agreement. A summary of agreement, uncertainty, or disagreement (derived from the group median score) and consensus (determined using the Interpercentile Range Adjusted for Symmetry method) was calculated for each statement and presented for discussion before individual rescoring. Key findings and limitations: Participants agreed that MRI scans must meet a minimum image quality standard (median 9) or be given a score of 'X' for insufficient quality. The current scan should be compared with both baseline and previous scans (median 9), with the PRECISE score being the maximum from any lesion (median 8). PRECISE 3 (stable MRI) was subdivided into 3-V (visible) and 3-NonV (nonvisible) disease (median 9). Prostate Imaging Reporting and Data System/Likert ≥3 lesions should be measured on T2-weighted imaging, using other sequences to aid in the identification (median 8), and whenever possible, reported pictorially (diagrams, screenshots, or contours; median 9). There was no consensus on how to measure tumour size. More research is needed to determine a significant size increase (median 9). PRECISE 5 was clarified as progression to stage ≥T3a (median 9). Conclusions and clinical implications: The updated PRECISE recommendations reflect expert consensus opinion on minimal standards and reporting criteria for prostate MRI in AS. Patient summary: The Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations are used in clinical practice and research to guide the interpretation and reporting of magnetic resonance imaging for patients on active surveillance for prostate cancer. An international panel has updated these recommendations, clarified the areas of uncertainty, and highlighted the areas for further research.

PRECISE Version 2: Updated Recommendations for Reporting Prostate Magnetic Resonance Imaging in Patients on Active Surveillance for Prostate Cancer / Englman, Cameron; Maffei, Davide; Allen, Clare; Kirkham, Alex; Albertsen, Peter; Kasivisvanathan, Veeru; Baroni, Ronaldo Hueb; Briganti, Alberto; De Visschere, Pieter; Dickinson, Louise; Gómez Rivas, Juan; Haider, Masoom A.; Kesch, Claudia; Loeb, Stacy; Macura, Katarzyna J.; Margolis, Daniel; Mitra, Anita M.; Padhani, Anwar R.; Panebianco, Valeria; Pinto, Peter A.; Ploussard, Guillaume; Puech, Philippe; Purysko, Andrei S.; Radtke, Jan Philipp; Rannikko, Antti; Rastinehad, Art; Renard-Penna, Raphaele; Sanguedolce, Francesco; Schimmöller, Lars; Schoots, Ivo G.; Shariat, Shahrokh F.; Schieda, Nicola; Tempany, Clare M.; Turkbey, Baris; Valerio, Massimo; Villers, Arnauld; Walz, Jochen; Barrett, Tristan; Giganti, Francesco; Moore, Caroline M.. - In: EUROPEAN UROLOGY. - ISSN 0302-2838. - (2024). [10.1016/j.eururo.2024.03.014]

PRECISE Version 2: Updated Recommendations for Reporting Prostate Magnetic Resonance Imaging in Patients on Active Surveillance for Prostate Cancer

Panebianco, Valeria;
2024

Abstract

Background and objective: The Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations standardise the reporting of prostate magnetic resonance imaging (MRI) in patients on active surveillance (AS) for prostate cancer. An international consensus group recently updated these recommendations and identified the areas of uncertainty. Methods: A panel of 38 experts used the formal RAND/UCLA Appropriateness Method consensus methodology. Panellists scored 193 statements using a 1-9 agreement scale, where 9 means full agreement. A summary of agreement, uncertainty, or disagreement (derived from the group median score) and consensus (determined using the Interpercentile Range Adjusted for Symmetry method) was calculated for each statement and presented for discussion before individual rescoring. Key findings and limitations: Participants agreed that MRI scans must meet a minimum image quality standard (median 9) or be given a score of 'X' for insufficient quality. The current scan should be compared with both baseline and previous scans (median 9), with the PRECISE score being the maximum from any lesion (median 8). PRECISE 3 (stable MRI) was subdivided into 3-V (visible) and 3-NonV (nonvisible) disease (median 9). Prostate Imaging Reporting and Data System/Likert ≥3 lesions should be measured on T2-weighted imaging, using other sequences to aid in the identification (median 8), and whenever possible, reported pictorially (diagrams, screenshots, or contours; median 9). There was no consensus on how to measure tumour size. More research is needed to determine a significant size increase (median 9). PRECISE 5 was clarified as progression to stage ≥T3a (median 9). Conclusions and clinical implications: The updated PRECISE recommendations reflect expert consensus opinion on minimal standards and reporting criteria for prostate MRI in AS. Patient summary: The Prostate Cancer Radiological Estimation of Change in Sequential Evaluation (PRECISE) recommendations are used in clinical practice and research to guide the interpretation and reporting of magnetic resonance imaging for patients on active surveillance for prostate cancer. An international panel has updated these recommendations, clarified the areas of uncertainty, and highlighted the areas for further research.
2024
Active surveillance; Consensus; Prostate cancer; Prostate magnetic resonance imaging
01 Pubblicazione su rivista::01a Articolo in rivista
PRECISE Version 2: Updated Recommendations for Reporting Prostate Magnetic Resonance Imaging in Patients on Active Surveillance for Prostate Cancer / Englman, Cameron; Maffei, Davide; Allen, Clare; Kirkham, Alex; Albertsen, Peter; Kasivisvanathan, Veeru; Baroni, Ronaldo Hueb; Briganti, Alberto; De Visschere, Pieter; Dickinson, Louise; Gómez Rivas, Juan; Haider, Masoom A.; Kesch, Claudia; Loeb, Stacy; Macura, Katarzyna J.; Margolis, Daniel; Mitra, Anita M.; Padhani, Anwar R.; Panebianco, Valeria; Pinto, Peter A.; Ploussard, Guillaume; Puech, Philippe; Purysko, Andrei S.; Radtke, Jan Philipp; Rannikko, Antti; Rastinehad, Art; Renard-Penna, Raphaele; Sanguedolce, Francesco; Schimmöller, Lars; Schoots, Ivo G.; Shariat, Shahrokh F.; Schieda, Nicola; Tempany, Clare M.; Turkbey, Baris; Valerio, Massimo; Villers, Arnauld; Walz, Jochen; Barrett, Tristan; Giganti, Francesco; Moore, Caroline M.. - In: EUROPEAN UROLOGY. - ISSN 0302-2838. - (2024). [10.1016/j.eururo.2024.03.014]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1710474
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