MRI-targeted or standard biopsy for prostate-cancer diagnosis

Authors

Veeru Kasivisvanathan, University College London
Antti S. Rannikko, Helsinki University Hospital
Marcelo Borghi, Centro de Urología
Valeria Panebianco, Università degli Studi di Roma La Sapienza
Lance A. Mynderse, Mayo Clin.
Markku H. Vaarala, Oulu University Hospital
Alberto Briganti, Università Vita-Salute San Raffaele
Lars Budäus, Universitätsklinikum Hamburg-Eppendorf und Medizinische Fakultät
Giles Hellawell, London North West University Healthcare NHS Trust
Richard G. Hindley, Hampshire Hospitals NHS Foundation Trust
Monique J. Roobol, Erasmus MC
Scott Eggener, The University of Chicago
Maneesh Ghei, Whittington Health NHS Trust
Arnauld Villers, CHU Lille
Franck Bladou, Sir Mortimer B. Davis Jewish General Hospital
Geert M. Villeirs, University Hospital of Ghent
Jaspal Virdi, The Princess Alexandra Hospital NHS Trust
Silvan Boxler, UniversitätsSpital Bern
Grégoire Robert, Université de Bordeaux
Paras B. Singh, Royal Free London NHS Foundation Trust
Wulphert Venderink, Radboud University Nijmegen Medical Centre
Boris A. Hadaschik, Universitäts Klinikum Essen und Medizinische Fakultät
Alain Ruffion, Centre Hospitalier Lyon-Sud
Jim C. Hu, New York Presbyterian Hospital
Daniel Margolis, New York Presbyterian Hospital
Sébastien Crouzet, CHU de Lyon
Laurence Klotz, Sunnybrook Health Sciences Centre
Samir S. Taneja, NYU Langone Health
Peter Pinto, National Institutes of Health (NIH)
Inderbir Gill, Keck School of Medicine of USC
Clare Allen, University College London
Francesco Giganti, University College London
Alex Freeman, University College London

Document Type

Journal Article

Publication Date

5-10-2018

Journal

New England Journal of Medicine

Volume

378

Issue

19

DOI

10.1056/NEJMoa1801993

Abstract

Copyright © 2018 Massachusetts Medical Society. BACKGROUND: Multiparametric magnetic resonance imaging (MRI), with or without targeted biopsy, is an alternative to standard transrectal ultrasonography-guided biopsy for prostate-cancer detection in men with a raised prostate-specific antigen level who have not undergone biopsy. However, comparative evidence is limited. METHODS: In a multicenter, randomized, noninferiority trial, we assigned men with a clinical suspicion of prostate cancer who had not undergone biopsy previously to undergo MRI, with or without targeted biopsy, or standard transrectal ultrasonography-guided biopsy. Men in the MRI-targeted biopsy group underwent a targeted biopsy (without standard biopsy cores) if the MRI was suggestive of prostate cancer; men whose MRI results were not suggestive of prostate cancer were not offered biopsy. Standard biopsy was a 10-to-12-core, transrectal ultrasonography-guided biopsy. The primary outcome was the proportion of men who received a diagnosis of clinically significant cancer. Secondary outcomes included the proportion of men who received a diagnosis of clinically insignificant cancer. RESULTS: A total of 500 men underwent randomization. In the MRI-targeted biopsy group, 71 of 252 men (28%) had MRI results that were not suggestive of prostate cancer, so they did not undergo biopsy. Clinically significant cancer was detected in 95 men (38%) in the MRI-targeted biopsy group, as compared with 64 of 248 (26%) in the standard-biopsy group (adjusted difference, 12 percentage points; 95% confidence interval [CI], 4 to 20; P = 0.005). MRI, with or without targeted biopsy, was noninferior to standard biopsy, and the 95% confidence interval indicated the superiority of this strategy over standard biopsy. Fewer men in the MRI-targeted biopsy group than in the standard-biopsy group received a diagnosis of clinically insignificant cancer (adjusted difference, -13 percentage points; 95% CI, -19 to -7; P<0.001). CONCLUSIONS: The use of risk assessment with MRI before biopsy and MRI-targeted biopsy was superior to standard transrectal ultrasonography-guided biopsy in men at clinical risk for prostate cancer who had not undergone biopsy previously. (Funded by the National Institute for Health Research and the European Association of Urology Research Foundation; PRECISION ClinicalTrials.gov number, NCT02380027.)

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