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The role of multiparametric MRI in active surveillance for low-risk prostate cancer: The ROMAS randomized controlled trial

Authors :
Michelangelo Fiorentino
Riccardo Schiavina
Marco Borghesi
Pietro Piazza
Eugenio Brunocilla
Rita Golfieri
Francesca Giunchi
Valeria Panebianco
Angelo Porreca
Paolo Verze
Cristian Vincenzo Pultrone
Beniamino Corcioni
M. Guerra
Lorenzo Bianchi
Matteo Droghetti
Federico Mineo Bianchi
Vincenzo Mirone
Caterina Gaudiano
Giacomo Novara
Schiavina, Riccardo
Droghetti, Matteo
Novara, Giacomo
Bianchi, Lorenzo
Gaudiano, Caterina
Panebianco, Valeria
Borghesi, Marco
Piazza, Pietro
Mineo Bianchi, Federico
Guerra, Marco
Corcioni, Beniamino
Fiorentino, Michelangelo
Giunchi, Francesca
Verze, Paolo
Pultrone, Cristian
Golfieri, Rita
Porreca, Angelo
Mirone, Vincenzo
Brunocilla, Eugenio
Schiavina, R.
Droghetti, M.
Novara, G.
Bianchi, L.
Gaudiano, C.
Panebianco, V.
Borghesi, M.
Piazza, P.
Mineo Bianchi, F.
Guerra, M.
Corcioni, B.
Fiorentino, M.
Giunchi, F.
Verze, P.
Pultrone, C.
Golfieri, R.
Porreca, A.
Mirone, V.
Brunocilla, E.
Publication Year :
2021

Abstract

Background: We aim to evaluate the impact of multiparametric magnetic resonance imaging and fusion-target biopsy for early reclassification of patients with low-risk Prostate Cancer in a randomized trial. Materials and methods: Between 2015 and 2018, patients diagnosed with Prostate Cancer after random biopsy fulfilling PRIAS criteria were enrolled and centrally randomized (1:1 ratio) to study group or control group. Patients randomized to study group underwent multiparametric magnetic resonance imaging at 3 months from enrollment: patients with positive findings (PIRADS-v2>2) underwent fusion-target biopsy; patients with negative multiparametric magnetic resonance imaging or confirmed ISUP - Grade Group 1 at fusion-target biopsy were managed according to PRIAS schedule and 12-core random biopsy was performed at 12 months. Patients in control group underwent PRIAS protocol, including a confirmatory 12-core random biopsy at 12 months. Primary endpoint was a reduction of reclassification rate at 12-month random biopsy in study group at least 20% less than controls. Reclassification was defined as biopsy ISUP Grade Group 1 in >2 biopsy cores or disease upgrading. Results: A total of 124 patients were randomized to study group (n = 62) or control group (n = 62). Around 21 of 62 patients (34%) in study group had a positive multiparametric magnetic resonance imaging, and underwent fusion-target biopsy, with 11 (17.7%) reclassifications. Considering the intention-to-treat population, reclassification rate at 12-month random biopsy was 6.5% for study group and 29% for control group, respectively (P < 0.001). Conclusions: The early employment of multiparametric magnetic resonance imaging for active surveillance patients enrolled after random biopsy consents to significantly reduce reclassifications at 12-month random biopsy.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....2370fa091279ac1a9af85d786f6f4127