Evidence map›Paper›PMID 40991040›Full record

ArticleWorld journal of urology2025

PSMA-PET/CT-based salvage elective nodal radiotherapy for lymph node recurrence following radical prostatectomy.

Samuel M Vorbach, Hannah Rittmayer, Thomas Seppi, Bernhard Nilica, Mona Kafka, Ute Ganswindt

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Article in World journal of urology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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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

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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

2 citing papers in PubMed.

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4 · The record

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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

6 authors.

Samuel M VorbachDepartment of Radiation Oncology, Medical University of Innsbruck, Innsbruck, Austria. samuel.vorbach@i-med.ac.at.ORCID http://orcid.org/0009-0003-1711-1604
Hannah RittmayerDepartment of Radiation Oncology, Medical University of Innsbruck, Innsbruck, Austria.
Thomas SeppiDepartment of Radiation Oncology, Medical University of Innsbruck, Innsbruck, Austria.
Bernhard NilicaDepartment of Nuclear Medicine, Medical University of Innsbruck, Innsbruck, Austria.
Mona Kafka *Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
Ute Ganswindt *Department of Radiation Oncology, Medical University of Innsbruck, Innsbruck, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeFor patients with oligometastatic nodal recurrence after radical prostatectomy (RP), salvage radiotherapy is a valuable curative second-line treatment option. However, few clinical data on the impact of PSMA-PET/CT-based salvage elective nodal radiotherapy (sENRT) is available. In order to contribute further clinical data on the outcome of patients treated with sENRT following RP, we analysed the rates of biochemical recurrence-free survival (BRFS) and distant metastasis-free survival (DMFS) as well as potential predictive markers for optimised patient selection.

methodsA retrospective analysis of 76 patients treated with sENRT for nodal recurrence after RP was performed. Primary endpoints were BRFS and DMFS. Cox proportional hazards model was used to analyse potential predictive factors.

resultsMedian follow-up was 32.6 months. PSMA-PET/CT revealed 1, 2, or ≥ 3 positive lymph nodes in 63.2%, 30.2% and 6.6% of patients, respectively. 96% of the patients had pelvic-only lymph nodes involvement. One-, two- and three-year BRFS were 98.6%, 84.2%, and 71.9%, respectively. Notably, nodal status at the time of RP and biochemical-recurrence prior to sENRT, were associated with reduced BRFS. One-, two-, and three-year DMFS were 98.7%, 94.1%, and 94.1%, respectively, with paraaortic lymph nodes being the only factor indicating reduced DMFS. Concomitant androgen-deprivation therapy was applied in 85.5% of the patients.

conclusionWe present one of the largest studies on PSMA-PET-based sENRT for nodal recurrence after RP with promising results, highlighting the important role of sENRT. Regarding patient selection, initial lymph node status and prior radiation of the prostate were predictive of reduced BRFS, while involvement of paraaortic lymph nodes was identified as marker for reduced DMFS.

Indexed as

Lymphatic MetastasisLymph NodesNeoplasm Recurrence, LocalPositron Emission Tomography Computed TomographyProstatectomyProstatic NeoplasmsSalvage TherapyAgedHumansMaleMiddle AgedRetrospective StudiesNodal recurrenceProstate cancerPSMA-PET/CTSalvage elective nodal radiotherapy

Identifiers

PMID40991040
PMCPMC12460443

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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.