Evidence map›Paper›PMID 39601084›Full record

ArticleJournal of magnetic resonance imaging : JMRI2025

Long-Term Risk of Clinically Significant Prostate Cancer in Biopsy-Negative Patients With Baseline Biparametric Prostate MRI.

Laura Parhiala, Juha Knaapila, Ivan Jambor, Janne Verho, Kari Syvänen, Hannu Aronen, Peter Boström, Otto Ettala

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Laura ParhialaDepartment of Urology, University of Turku, Turku, Finland.ORCID 0009-0009-6871-9373
Juha KnaapilaDepartment of Urology, Kuopio University Hospital, Kuopio, Finland.ORCID 0000-0003-0997-9668
Ivan JamborDepartment of Diagnostic Radiology, University of Turku, Turku, Finland.ORCID 0000-0001-6305-3570
Janne VerhoDepartment of Diagnostic Radiology, University of Turku, Turku, Finland.
Kari SyvänenDepartment of Urology, University of Turku, Turku, Finland.
Hannu AronenDepartment of Diagnostic Radiology, University of Turku, Turku, Finland.
Peter BoströmDepartment of Urology, University of Turku, Turku, Finland.
Otto EttalaDepartment of Urology, University of Turku, Turku, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe long-term prevalence of clinically significant prostate cancer (csPCa) in patients with initial negative prostate biopsy is unknown. PURPOSE: To investigate the rate of csPCa of men with initial negative biopsy. STUDY TYPE: Retrospective analysis of prospectively collected data. POPULATION: A total of 197 men (mean age 63 years [SD ±6.98, range 29-79]) without csPCa on initial biopsy and available baseline biparametric prostate MRI (bpMRI). FIELD STRENGTH/SEQUENCE: 3.0 T, turbo spin-echo T2-weighted (axial and sagittal) and three sets of diffusion-weighted imaging using single-shot spin-echo planar imaging (5 b-values 0-500 seconds/mm ASSESSMENT: BpMRI was read using Prostate Imaging Reporting Data System (PI-RADS) v2.1. Systematic or targeted biopsy results served as reference standard. STATISTICAL TESTS: Continuous variables were compared using Kruskal-Wallis rank sum test. Categorical variables were compared using either Fisher's exact test or Pearson's chi-square test. Uni- and multivariate regression odds ratios (95% confidence interval) were used to study factors affecting csPCa being diagnosed during follow-up. Time to diagnosis of csPCa is calculated using the Kaplan-Meier method.

resultsOf 197 men, 74 (38%), 57 (29%), and 66 (34%) presented with PI-RADS 1-2, 3, and 4-5 findings in the baseline bpMRI. During the median follow-up of 52 months, 8.1%, 5.3%, and 18.2% of these men were diagnosed with csPCa, respectively. Baseline PI-RADS finding was the only factor that associated with csPCa found during the follow-up. DATA

conclusionBaseline bpMRI with PI-RADS scores 1-3 and initial biopsies negative of csPCa had low rate of csPCa during follow-up, which supports more conservative follow-up for them but further research with longer follow-up is warranted. LEVEL OF EVIDENCE: 3 TECHNICAL EFFICACY: Stage 2.

Indexed as

Magnetic Resonance ImagingProstatic NeoplasmsAdultAgedBiopsyHumansImage-Guided BiopsyMaleMiddle AgedProstateRetrospective StudiesRisk Factors

Identifiers

PMID39601084
PMCPMC12063762

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.