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

Authors :
Jambor I
Verho J
Ettala O
Knaapila J
Taimen P
Syvänen KT
Kiviniemi A
Kähkönen E
Perez IM
Seppänen M
Rannikko A
Oksanen O
Riikonen J
Vimpeli SM
Kauko T
Merisaari H
Kallajoki M
Mirtti T
Lamminen T
Saunavaara J
Aronen HJ
Boström PJ
Source :
PLoS medicine [PLoS Med] 2019 Jun 03; Vol. 16 (6), pp. e1002813. Date of Electronic Publication: 2019 Jun 03 (Print Publication: 2019).
Publication Year :
2019

Abstract

Background: Magnetic 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.<br />Methods and Findings: The 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.<br />Conclusions: IMPROD bpMRI demonstrated a high NPV for SPCa in men with a clinical suspicion of PCa in this prospective multi-institutional clinical trial.<br />Trial Registration: ClinicalTrials.gov NCT02241122.<br />Competing Interests: The authors have declared that no competing interests exist.

Details

Language :
English
ISSN :
1549-1676
Volume :
16
Issue :
6
Database :
MEDLINE
Journal :
PLoS medicine
Publication Type :
Academic Journal
Accession number :
31158230
Full Text :
https://doi.org/10.1371/journal.pmed.1002813