Evidence map›Paper›PMID 41228237›Full record

ArticleCancers2025

Upstaging of Patients Diagnosed with Favorable Intermediate-Risk Prostate Cancer-Is Active Surveillance Really a Suitable Approach for All These Patients?

Analena E Handke, Christopher Orf, Martina Dellino, Leon Miguel Garcia-Schürmann, Jan Philipp Radtke, Joachim Noldus, Florian Roghmann, Rein-Jüri Palisaar, Sebastian Berg, Karl H Tully

Abstract read
In one paragraph

Article in Cancers, 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. Article
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

10 authors.

Analena E HandkeDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Christopher OrfDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Martina DellinoDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Leon Miguel Garcia-SchürmannDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Jan Philipp RadtkeDepartment of Urology, University Hospital Duesseldorf, Heinrich-Heine-University Duesseldorf, 40225 Duesseldorf, Germany.
Joachim NoldusDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Florian RoghmannDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.ORCID 0000-0003-0299-489X
Rein-Jüri PalisaarDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Sebastian BergDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.
Karl H TullyDepartment of Urology and Neurourology, Marien Hospital Herne, Ruhr-University Bochum, 44801 Bochum, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND &

objectivesCurrent guidelines recognize a subgroup of favorable intermediate-risk (FIR) ISUP grade group (GG) 2 prostate cancer (PCa) that may be eligible for active surveillance (AS). However, upgrading and upstaging to more aggressive disease are frequently observed. We aimed to identify risk factors for adverse pathology in this cohort to better define clinical scenarios where AS may need to be reconsidered.

methodsWe retrospectively analyzed 170 patients diagnosed with ISUP GG2 PCa by multiparametric MRI (mpMRI)/TRUS fusion biopsy, all treated with radical prostatectomy (RP). Patients with FIR disease were evaluated for upstaging to ≥pT3 or upgrading to ISUP GG of ≥3 at RP. Multivariable logistic regression identified predictors of adverse pathology. Key Findings and Limitations: Among 170 FIR patients, median PSA was 5.6 ng/mL. Most had PI-RADS 4 (57%) or 5 (20%) lesions; 13% were diagnosed by systematic biopsy only. At RP, 28% showed adverse pathology, including 5 patients (2.9%) with lymph node metastases. Independent predictors were a PI-RADS Score of ≥4, PSA of >7 ng/mL, and clinical T-stage on digital rectal examination. CONCLUSIONS AND CLINICAL IMPLICATIONS: Nearly 1/3 of FIR PCa patients were upstaged to high-risk PCa at RP. Based on these findings, AS in clinical practice should only be considered after thorough patient counseling and performed using a stringent follow-up and staging regimen to minimize the risk of further disease progression. A key limitation is the lack of the percentage of Gleason pattern 4.

Indexed as

active surveillancefavorable intermediate-riskmpMRIPI-RADSprostate cancerupgradingupstaging

Identifiers

PMID41228237
PMCPMC12607737

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Registered trials

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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.