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Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial

OBJECTIVES: Our objective was to compare prostate cancer detection rates between patients undergoing serum prostate-specific antigen (PSA) vs magnetic resonance imaging (MRI) for prostate cancer screening. DESIGN: Phase III open-label randomised controlled trial. SETTING: Single tertiary cancer cent...

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Autores principales: Nam, Robert, Patel, Chirag, Milot, Laurent, Hird, Amanda, Wallis, Christopher, Macinnis, Patrick, Singh, Mala, Emmenegger, Urban, Sherman, Christopher, Haider, Masoom A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644313/
https://www.ncbi.nlm.nih.gov/pubmed/36351725
http://dx.doi.org/10.1136/bmjopen-2021-059482
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author Nam, Robert
Patel, Chirag
Milot, Laurent
Hird, Amanda
Wallis, Christopher
Macinnis, Patrick
Singh, Mala
Emmenegger, Urban
Sherman, Christopher
Haider, Masoom A
author_facet Nam, Robert
Patel, Chirag
Milot, Laurent
Hird, Amanda
Wallis, Christopher
Macinnis, Patrick
Singh, Mala
Emmenegger, Urban
Sherman, Christopher
Haider, Masoom A
author_sort Nam, Robert
collection PubMed
description OBJECTIVES: Our objective was to compare prostate cancer detection rates between patients undergoing serum prostate-specific antigen (PSA) vs magnetic resonance imaging (MRI) for prostate cancer screening. DESIGN: Phase III open-label randomised controlled trial. SETTING: Single tertiary cancer centre in Toronto, Canada. PARTICIPANTS: Men 50 years of age and older with no history of PSA screening for ≥3 years, a negative digital rectal exam and no prior prostate biopsy. INTERVENTIONS: Patients were recommended to undergo a prostate biopsy if their PSA was ≥2.6 ng/mL (PSA arm) or if they had a PIRADS score of 4 or 5 (MRI arm). Patients underwent an end-of-study PSA in the MRI arm. PRIMARY AND SECONDARY OUTCOME MEASURES: Adenocarcinoma on prostate biopsy. Prostate biopsy rates and the presence of clinically significant prostate cancer were also compared. RESULTS: A total of 525 patients were randomised, with 266 in the PSA arm and 248 in the MRI arm. Due to challenges with accrual and study execution during the COVID-19 pandemic, the study was terminated early. In the PSA arm, 48 patients had an abnormal PSA and 28 (58%) agreed to undergo a prostate biopsy. In the MRI arm, 25 patients had a PIRADS score of 4 or 5 and 24 (96%) agreed to undergo a biopsy. The relative risk for MRI to recommend a prostate biopsy was 0.52 (95% CI 0.33 to 0.82, p=0.005), compared with PSA. The cancer detection rate for patients in the PSA arm was 29% (8 of 28) vs 63% (15 of 24, p=0.019) in the MRI arm, with a higher proportion of clinically significant cancer detected in the MRI arm (73% vs 50%). The relative risk for detecting cancer and clinically significant with MRI compared with PSA was 1.89 (95% CI 0.82 to 4.38, p=0.14) and 2.77 (95% CI 0.89 to 8.59, p=0.07), respectively. CONCLUSIONS: Prostate MRI as a stand-alone screening test reduced the rate of prostate biopsy. The number of clinically significant cancers detected was higher in the MRI arm, but this did not reach statistical significance. Due to early termination, the study was underpowered. More patients were willing to follow recommendations for prostate biopsy based on MRI results. TRIAL REGISTRATION NUMBER: NCT02799303.
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spelling pubmed-96443132022-11-15 Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial Nam, Robert Patel, Chirag Milot, Laurent Hird, Amanda Wallis, Christopher Macinnis, Patrick Singh, Mala Emmenegger, Urban Sherman, Christopher Haider, Masoom A BMJ Open Urology OBJECTIVES: Our objective was to compare prostate cancer detection rates between patients undergoing serum prostate-specific antigen (PSA) vs magnetic resonance imaging (MRI) for prostate cancer screening. DESIGN: Phase III open-label randomised controlled trial. SETTING: Single tertiary cancer centre in Toronto, Canada. PARTICIPANTS: Men 50 years of age and older with no history of PSA screening for ≥3 years, a negative digital rectal exam and no prior prostate biopsy. INTERVENTIONS: Patients were recommended to undergo a prostate biopsy if their PSA was ≥2.6 ng/mL (PSA arm) or if they had a PIRADS score of 4 or 5 (MRI arm). Patients underwent an end-of-study PSA in the MRI arm. PRIMARY AND SECONDARY OUTCOME MEASURES: Adenocarcinoma on prostate biopsy. Prostate biopsy rates and the presence of clinically significant prostate cancer were also compared. RESULTS: A total of 525 patients were randomised, with 266 in the PSA arm and 248 in the MRI arm. Due to challenges with accrual and study execution during the COVID-19 pandemic, the study was terminated early. In the PSA arm, 48 patients had an abnormal PSA and 28 (58%) agreed to undergo a prostate biopsy. In the MRI arm, 25 patients had a PIRADS score of 4 or 5 and 24 (96%) agreed to undergo a biopsy. The relative risk for MRI to recommend a prostate biopsy was 0.52 (95% CI 0.33 to 0.82, p=0.005), compared with PSA. The cancer detection rate for patients in the PSA arm was 29% (8 of 28) vs 63% (15 of 24, p=0.019) in the MRI arm, with a higher proportion of clinically significant cancer detected in the MRI arm (73% vs 50%). The relative risk for detecting cancer and clinically significant with MRI compared with PSA was 1.89 (95% CI 0.82 to 4.38, p=0.14) and 2.77 (95% CI 0.89 to 8.59, p=0.07), respectively. CONCLUSIONS: Prostate MRI as a stand-alone screening test reduced the rate of prostate biopsy. The number of clinically significant cancers detected was higher in the MRI arm, but this did not reach statistical significance. Due to early termination, the study was underpowered. More patients were willing to follow recommendations for prostate biopsy based on MRI results. TRIAL REGISTRATION NUMBER: NCT02799303. BMJ Publishing Group 2022-11-08 /pmc/articles/PMC9644313/ /pubmed/36351725 http://dx.doi.org/10.1136/bmjopen-2021-059482 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Urology
Nam, Robert
Patel, Chirag
Milot, Laurent
Hird, Amanda
Wallis, Christopher
Macinnis, Patrick
Singh, Mala
Emmenegger, Urban
Sherman, Christopher
Haider, Masoom A
Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title_full Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title_fullStr Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title_full_unstemmed Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title_short Prostate MRI versus PSA screening for prostate cancer detection (the MVP Study): a randomised clinical trial
title_sort prostate mri versus psa screening for prostate cancer detection (the mvp study): a randomised clinical trial
topic Urology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9644313/
https://www.ncbi.nlm.nih.gov/pubmed/36351725
http://dx.doi.org/10.1136/bmjopen-2021-059482
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