MRI-targeted or standard biopsy for prostate-cancer diagnosis

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Kasivisvanathan Veeru, Rannikko Antti S, Borghi Marcelo, Panebianco Valeria, Mynderse Lance A, Vaarala Markku H, Briganti Alberto, Budäus Lars, Hellawell Giles, Hindley Richard G, Roobol Monique J, Eggener Scott, Ghei Maneesh, Villers Arnauld, Bladou Franck, Villeirs Geert M, Virdi Jaspal, Boxler Silvan, Robert Grégoire, Singh Paras B, Venderink Wulphert, Hadaschik Boris A, Ruffion Alain, Jim C Hu, Margolis Daniel, Crouzet Sébastien, Klotz Laurence, Taneja Samir S, Pinto Peter, Gill Inderbir, Allen Clare, Giganti Francesco, Freeman Alex, Morris Stephen, Punwani Shonit, Williams Norman R, Brew-Graves Chris, Deeks Jonathan, Takwoingi Yemisi, Emberton Mark, Moore Caroline M, Precision Study Group Collaborators, Catalano Carlo, Leonardo Costantino, Sciarra Alessandro, Grompone Marcello Domenico, Del Monte Maurizio, D'Eramo Giuseppe, Salvo Vincenzo, Campa Riccardo
ISSN: 0028-4793

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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