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Validation of IMPROD biparametric MRI in men with clinically suspected prostate cancer : A prospective multi-institutional trial

Validation of IMPROD biparametric MRI in men with clinically suspected prostate cancer : A prospective multi-institutional trial

Authors :
Harri Merisaari
Peter J. Boström
Otto Ettala
Outi Oksanen
Kari T. Syvänen
Hannu J. Aronen
Antti Rannikko
Janne Verho
Aida Kiviniemi
Ivan Jambor
Sanna Mari Vimpeli
Juha Knaapila
Ileana Montoya Perez
Jarno Riikonen
Markku Kallajoki
Jani Saunavaara
Esa Kähkönen
Pekka Taimen
Tarja Lamminen
Marjo Seppänen
Tuomas Mirtti
Tommi Kauko
HUS Abdominal Center
University Management
Urologian yksikkö
Department of Surgery
University of Helsinki
HUS Medical Imaging Center
Department of Diagnostics and Therapeutics
Research Program in Systems Oncology
HUSLAB
Department of Pathology
Source :
PLoS Medicine, Vol 16, Iss 6, p e1002813 (2019)
Publication Year :
2019

Abstract

BackgroundMagnetic resonance imaging (MRI) combined with targeted biopsy (TB) is increasingly used in men with clinically suspected prostate cancer (PCa), but the long acquisition times, high costs, and inter-center/reader variability of routine multiparametric prostate MRI limit its wider adoption.Methods and findingsThe aim was to validate a previously developed unique MRI acquisition and reporting protocol, IMPROD biparametric MRI (bpMRI) (NCT01864135), in men with a clinical suspicion of PCa in a multi-institutional trial (NCT02241122). IMPROD bpMRI has average acquisition time of 15 minutes (no endorectal coil, no intravenous contrast use) and consists of T2-weighted imaging and 3 separate diffusion-weighed imaging acquisitions. Between February 1, 2015, and March 31, 2017, 364 men with a clinical suspicion of PCa were enrolled at 4 institutions in Finland. Men with an equivocal to high suspicion (IMPROD bpMRI Likert score 3-5) of PCa had 2 TBs of up to 2 lesions followed by a systematic biopsy (SB). Men with a low to very low suspicion (IMPROD bpMRI Likert score 1-2) had only SB. All data and protocols are freely available. The primary outcome of the trial was diagnostic accuracy-including overall accuracy, sensitivity, specificity, negative predictive value (NPV), and positive predictive value-of IMPROD bpMRI for clinically significant PCa (SPCa), which was defined as a Gleason score ≥ 3 + 4 (Gleason grade group 2 or higher). In total, 338 (338/364, 93%) prospectively enrolled men completed the trial. The accuracy and NPV of IMPROD bpMRI for SPCa were 70% (113/161) and 95% (71/75) (95% CI 87%-98%), respectively. Restricting the biopsy to men with equivocal to highly suspicious IMPROD bpMRI findings would have resulted in a 22% (75/338) reduction in the number of men undergoing biopsy while missing 4 (3%, 4/146) men with SPCa. The main limitation is uncertainty about the true PCa prevalence in the study cohort, since some of the men may have PCa despite having negative biopsy findings.ConclusionsIMPROD bpMRI demonstrated a high NPV for SPCa in men with a clinical suspicion of PCa in this prospective multi-institutional clinical trial.Trial registrationClinicalTrials.gov NCT02241122.

Details

Language :
English
Database :
OpenAIRE
Journal :
PLoS Medicine, Vol 16, Iss 6, p e1002813 (2019)
Accession number :
edsair.doi.dedup.....7c7a30d9dc7da79d78c788d82ed39edc