Evidence map›Paper›PMID 41383881›Full record

ArticleBJUI compass2025

Anatomical distribution of disease in pN1 prostate cancer with BCR post-RP: A PSMA-PET/CT-based analysis.

Lotte G Zuur, Katelijne C C de Bie, Lieke Wever, Anne-Claire Berrens, Jean-Paul A van Basten, Harm H E van Melick, Maarten L Donswijk, Daniela E Oprea-Lager, Wouter V Vogel, Henk G van der Poel and 2 more

Abstract read
In one paragraph

Article in BJUI compass, 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

12 authors.

Lotte G ZuurDepartment of Surgical Oncology (Urology) Netherlands Cancer Institute Amsterdam the Netherlands.ORCID https://orcid.org/0009-0000-7392-1626
Katelijne C C de BieDepartment of Urology Amsterdam University Medical Centre Amsterdam the Netherlands.
Lieke WeverDepartment of Urology Amsterdam University Medical Centre Amsterdam the Netherlands.
Anne-Claire BerrensDepartment of Surgical Oncology (Urology) Netherlands Cancer Institute Amsterdam the Netherlands.
Jean-Paul A van BastenDepartment of Urology Canisius Wilhelmina Hospital Nijmegen the Netherlands.
Harm H E van MelickDepartment of Urology St. Antonius Hospital, Utrecht Nieuwegein the Netherlands.
Maarten L DonswijkDepartment of Nuclear Medicine Netherlands Cancer Institute Amsterdam the Netherlands.
Daniela E Oprea-LagerDepartment of Medical Imaging Radboud University Medical Center Nijmegen the Netherlands.ORCID https://orcid.org/0000-0001-9447-2305
Wouter V VogelDepartment of Nuclear Medicine Netherlands Cancer Institute Amsterdam the Netherlands.
Henk G van der PoelDepartment of Surgical Oncology (Urology) Netherlands Cancer Institute Amsterdam the Netherlands.ORCID https://orcid.org/0000-0002-8772-1120
André N VisDepartment of Urology Amsterdam University Medical Centre Amsterdam the Netherlands.
Pim J van LeeuwenDepartment of Surgical Oncology (Urology) Netherlands Cancer Institute Amsterdam the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: To explore the distribution of metastatic disease in pN1 patients with biochemical recurrence (BCR) assessed by Prostate-Specific Membrane Antigen-Positron-Emission/Computed Tomography (PSMA-PET/CT). Patients and Methods: This multicentre, retrospective cohort study included 130 pN1 PCa patients with BCR (PSA ≥ 0.2 ng/ml) post-RP with ePLND (2015-2022). All were preoperatively staged as molecular imaging (mi)N0M0 and underwent restaging PSMA-PET/CT at BCR. Clinical and imaging data were analysed using Mann-Whitney U, chi-square tests and Cox regression. Results: Median time to BCR was 9 months (IQR 3-18). Biochemical persistence (BCP) (PSA ≥ 0.1 ng/ml at first follow-up) occurred in 66/130 (51%). At restaging PSMA-PET/CT, median PSA was 0.33 ng/ml (IQR 0.24-0.65). PSMA-PET/CT identified metastases in 63/130 (48%), with 37/63 (59%) having lymph node metastases (LNMs) limited to the ePLND template - 16/37 (43%) on the ipsilateral side of the positive resected node. Additionally, 26/63 (41%) had disease beyond the nodal template (miM+). Univariate Cox regression identified BCP as a predictor for any PSMA-PET/CT-detected recurrence, while a higher ISUP grade group at RP predicted miM+ disease. Conclusion: PSMA-PET/CT identified PSMA-expressing recurrent disease in nearly half of pN1 PCa patients at early BCR, with about half confined to the pelvis and a quarter beyond the pelvis. These anatomical patterns indicate that PSMA-PET/CT can inform risk-adapted salvage strategies, including pelvic radiotherapy for nodal recurrences and systemic treatment when disease extends beyond the pelvis.

Indexed as

node‐positiveprostate cancerprostate‐specific membrane antigen (PSMA)recurrence

Identifiers

PMID41383881
PMCPMC12690614

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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.