ArticleJAMA network open2026
Performance of MRI-Based vs Clinical T Staging in Localized Prostate Cancer.
Article in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Importance: Magnetic resonance imaging (MRI) is increasingly used for local staging in prostate cancer, yet its value relative to digital rectal examination (DRE) staging remains uncertain. Objectives: To compare the performance of MRI-based vs DRE-based clinical T staging in men undergoing radical prostatectomy (RP) and to assess the outcome of substituting MRI staging in established prognostic classification systems. Design, Setting, and Participants: This multicenter, retrospective case-control study (iTNM Consortium) was conducted from January 1, 2015, to December 31, 2021, among consecutive men 18 years or older with clinically localized or locally advanced prostate cancer who underwent RP and preoperative multiparametric MRI and systematic biopsies with or without targeted biopsies at 31 referral centers across 6 European countries. Patients receiving prior prostate cancer treatment or missing key variables were excluded. Data analysis was performed from August to October 2025. Exposures: MRI-derived T stage (iT) vs DRE-derived T stage (cT) incorporated into D'Amico, European Association of Urology, National Comprehensive Cancer Network, and International Staging Collaboration for Prostate Cancer risk groups to generate MRI-adapted classification systems. Main Outcomes and Measures: Primary outcome was distant metastasis-free survival. Secondary outcomes were biochemical recurrence-free survival and overall survival. Discrimination was assessed using a C index and time-dependent area under the receiver operating characteristic curves. Results: A total of 4425 men were included (median [IQR] age, 66 [61-70] years; median [IQR] prostate-specific antigen, 7.4 [5.5-10.5] ng/mL). Median (95% CI) follow-up was 52 (51-53) months. MRI-based staging showed slightly higher discriminatory ability than DRE staging for biochemical recurrence-free survival (C index, 0.62 [95% CI, 0.61-0.64] vs 0.59 [95% CI, 0.57-0.61]) and distant metastasis-free survival (0.67 [95% CI, 0.64-0.70] vs 0.65 [95% CI, 0.62-0.68]). However, across all 4 risk classification systems, MRI-based and DRE-based versions demonstrated comparable discrimination with overlapping 95% CIs. Time-dependent area under the receiver operating characteristic curves showed no significant difference during follow-up. Subgroup analyses of patients with cT1 disease and those with PSA levels less than 10 ng/mL yielded similar results. Conclusions and Relevance: In this case-control study of patients undergoing radical prostatectomy, MRI-based staging demonstrated discrimination similar to traditional DRE-based staging for biochemical recurrence, distant metastasis, and overall survival. These findings suggested that MRI-derived staging could be safely integrated into contemporary risk systems without compromising accuracy.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.