Evidence map›Paper›PMID 41741677›Full record

ArticleProstate cancer and prostatic diseases2026

PSMA-PET imaging in prostate cancer patients with high-risk biochemical recurrence: implications from an "EMBARK-Like" cohort.

Matteo Droghetti, Valerio Pirelli, Francesco Ceci, Andrea Farolfi, Matteo Bauckneht, Francesco Lanfranchi, Andrea Di Giorgio, Paolo Castellucci, Caterina Maria Paola Sgro, Carlos Artigas and 19 more

Abstract read
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In one paragraph

Article in Prostate cancer and prostatic diseases, 2026. 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. Insights from EMBARK: guiding clinical care and trial design.Translational andrology and urology · 2026
    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

29 authors.

Matteo Droghetti *Division of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy. droghet@gmail.com.ORCID http://orcid.org/0000-0002-9190-4691
Valerio Pirelli *Division of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Francesco CeciDivision of Nuclear Medicine and Theranostics, IEO European Institute of Oncology IRCCS, Milan, Italy.ORCID http://orcid.org/0000-0001-9785-5248
Andrea FarolfiNuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Matteo BaucknehtDepartment of Health Sciences (DISSAL), University of Genoa, Genoa, Italy.ORCID http://orcid.org/0000-0002-1937-9116
Francesco LanfranchiDepartment of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.ORCID http://orcid.org/0000-0002-6043-9627
Andrea Di GiorgioNuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID http://orcid.org/0009-0006-3973-4409
Paolo CastellucciNuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Caterina Maria Paola SgroNuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Carlos ArtigasDepartment of Nuclear Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Jose LeitePET/CT Center, DASA-Diagnósticos da América, Rio de Janeiro, Brazil.
Paola CoronaFundación Centro Diagnóstico Nuclear (FCDN), Buenos Aires, Argentina.ORCID http://orcid.org/0000-0001-8221-0295
Qaid Ahmed ShageraDepartment of Nuclear Medicine, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.
Renata MoreiraPET/CT Center, DASA-Diagnósticos da América, Rio de Janeiro, Brazil.
Christian GonzálezFundación Centro Diagnóstico Nuclear (FCDN), Buenos Aires, Argentina.
Marcelo QueirozDepartment of Radiology, Hospital Sírio-Libanês, Sao Paulo, Brazil.
Felipe de Galiza BarbosaDepartment of Radiology, Hospital Sírio-Libanês, Sao Paulo, Brazil.
Guido RoveraNuclear Medicine, Department of Medical Sciences, University of Turin, Turin, Italy.ORCID http://orcid.org/0000-0003-1839-0206
Desiree DeandreisNuclear Medicine, Institut Gustave-Roussy, Université Paris-Saclay, Villejuif, France.
Sara TamburiniDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Lorenzo NanniDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Federico BevilacquaDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Pietro PiazzaDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0002-6740-534X
Angelo MottaranDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Veronica MollicaMedical Oncology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Francesco MassariMedical Oncology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.
Stefano FantiNuclear Medicine, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Lorenzo BianchiDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.ORCID http://orcid.org/0000-0001-7321-1536
Riccardo SchiavinaDivision of Urology, IRCCS Azienda Ospedaliero Universitaria di Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The EMBARK trial demonstrated improved survival with enzalutamide plus androgen deprivation therapy (ADT) in non-metastatic hormone-sensitive prostate cancer patients with high-risk biochemical recurrence (BCR), although staged using conventional imaging. Given the higher sensitivity of PSMA-PET, many of these patients could harbor metastatic disease. We retrospectively analyzed 587 patients with first BCR after radical treatment who underwent PSMA-PET. Patients were stratified according to EMBARK criteria for high-risk BCR. 169 patients (29%) met EMBARK criteria. They more often showed PSMA-PET positivity for any localization (82% vs 39%; p < 0.001) and metastatic disease (46% vs 15%; p < 0.001). Median PSA was higher and PSA doubling-time (PSADT) shorter (2.23 vs 0.43 ng/mL; 4.3 vs 9 months). Most High-risk BCR patients have a positive PSMA-PET, and many of these harbor metastatic disease at molecular imaging. Given the survival benefit from intensified systemic treatment with ARPI in this cohort, how to best combine systemic therapy with PSMA-PET guided metastases-directed-treatments remains an important future area of research.

Indexed as

Antigens, SurfaceGlutamate Carboxypeptidase IINeoplasm Recurrence, LocalPositron-Emission TomographyProstatic NeoplasmsAgedAged, 80 and overHumansMaleMiddle AgedProstate-Specific AntigenRetrospective StudiesAntigens, SurfaceFOLH1 protein, humanGlutamate Carboxypeptidase IIProstate-Specific Antigen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.