Evidence map›Paper›PMID 41805998›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Omitted staging PSMA PET/CT is associated with advance disease extent at time of PSA persistence: a single center retrospective analysis.

Andrea Di Giorgio, Marco Rapa, Martina Di Franco, Caterina Maria Paola Sgro, Giambattista Siepe, Veronica Mollica, Lorenzo Bianchi, Matteo Droghetti, Paolo Castellucci, Riccardo Mei and 3 more

Abstract read
In one paragraph

Article in European journal of nuclear medicine and molecular imaging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Andrea Di GiorgioNuclear Medicine, Alma Mater Studiorum, University of Bologna, Via Massarenti 9, Bologna, 40138, Italy. andrea.digiorgio2@studio.unibo.it.
Marco RapaNuclear Medicine, Alma Mater Studiorum, University of Bologna, Via Massarenti 9, Bologna, 40138, Italy.
Martina Di FrancoNuclear Medicine, Alma Mater Studiorum, University of Bologna, Via Massarenti 9, Bologna, 40138, Italy.
Caterina Maria Paola SgroNuclear Medicine, Alma Mater Studiorum, University of Bologna, Via Massarenti 9, Bologna, 40138, Italy.
Giambattista SiepeRadiation Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Veronica MollicaMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Lorenzo BianchiDivision of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna, Bologna, Italy.
Matteo DroghettiDivision of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna, Bologna, Italy.
Paolo CastellucciNuclear Medicine, IRCCS, Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Riccardo MeiNuclear Medicine, IRCCS, Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Andrea FarolfiNuclear Medicine, IRCCS, Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy.
Riccardo SchiavinaDivision of Urology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, University of Bologna, Bologna, Italy.
Stefano FantiNuclear Medicine, Alma Mater Studiorum, University of Bologna, Via Massarenti 9, Bologna, 40138, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPSMA PET has emerged as a crucial imaging modality for staging intermediate- and high-risk prostate cancer (PCa), yet its implementation varies globally. This study aims to assess the diagnostic consequence of omitting pre-operative PSMA PET/CT staging by comparing the radiological features and extent of disease in two cohorts of patients who subsequently developed PSA persistence (> 0.1 ng/mL) following radical prostatectomy (RP). MATERIALS AND

methodsSingle-center, retrospective study (October 2019 to May 2025). The patient cohort included individuals who underwent radical prostatectomy and subsequently experienced PSA persistence, defined as a PSA value ≥ 0.1 ng/ml at the first measurement after 4–8 weeks after RP. Patients were divided into two groups: a Staging Cohort who underwent a pre-operative [68Ga]Ga-PSMA-11 PET/CT and a Non-Staging Cohort who did not. All patients received a [68Ga]Ga-PSMA-11PET/CT scan for PSA persistence. Clinical data, including PSA, TNM stage, and ISUP grade, as well as follow-up data were collected. The primary endpoints were the comparison of the overall PSMA PET positivity rate and the extent of both locoregional (N) and distant metastatic (M1) disease between the two cohorts. Secondary analysis included a comparison of baseline pathological characteristics and the evaluation of the potential for a theoretical change in initial patient management.

results147 patients with PSA persistence after RP were included and divided into the Staging Cohort (n = 72, 49%) and a Non-Staging Cohort (n = 75, 51%). Baseline data showed the Staging Cohort had a higher proportion of high-grade (ISUP 4/5:72% vs. 45%; p < 0.05 ) and locally advanced (T3/T4: 78% vs. 61%; p < 0.05) disease. The Non-Staging Cohort had a higher rate of positive [68Ga]Ga-PSMA-11 PET/CT scans for persistence (59%) compared to the Staging-Cohort (42%). The Non-Staging Cohort showed a markedly greater extent of disease, with a high proportion of patients (n = 34/75,45%) demonstrating findings consistent with M1 disease (bone or distant lymph nodes). The anatomical distribution of positive lymph node sites also differed: the Staging Cohort showed higher obturator nodes involvement (48% of positive sites), while the Non-Staging Cohort had a significantly higher proportion in common iliac (34%) and external/internal iliac sites. A retrospective evaluation of the Non-Staging Cohort suggested that a pre-operative [68Ga]Ga-PSMA-11 PET/CT would have triggered a theoretical change of management in all 44 positive cases, primarily by suggesting systemic therapy instead of RP for M1 patients.

conclusionThe omission of pre-operative [68Ga]Ga-PSMA-11 PET/CT is associated with a significantly higher incidence of PSMA-positive and extensive disease (locoregional and metastatic) at the time of PSA persistence. This suggests a critical diagnostic gap and potential under-staging in the Non-Staging Cohort, underscoring the vital role of early PSMA PET/CT utilization to optimize initial risk stratification and treatment planning.

Indexed as

OligopeptidesPositron Emission Tomography Computed TomographyProstate-Specific AntigenProstatic NeoplasmsAgedEdetic AcidGallium IsotopesGallium RadioisotopesHumansMaleMiddle AgedNeoplasm StagingRetrospective StudiesEdetic Acidgallium 68 PSMA-11Gallium IsotopesGallium RadioisotopesOligopeptidesProstate-Specific AntigenIntermediate RiskPersistence DiseaseProstate CancerPSMA PET/CTStaging

Identifiers

PMID41805998
PMCPMC13249642

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