Evidence map›Paper›PMID 41762267›Full record

Trial reportEuropean journal of nuclear medicine and molecular imaging2026

[

Wietske I Luining, André N Vis, Maarten L Donswijk, Jose C C Koppes, Pim J van Leeuwen, Frederik Oudshoorn, Matthijs C F Cysouw, Daniela E Oprea-Lager

Abstract readComparative StudyClinical Trial
In one paragraph

Trial report 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.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

8 authors.

Wietske I LuiningDepartment of Urology, Amsterdam University Medical Center, VU university, location VUmc, De Boelelaan 1117, 1081 HV , Amsterdam, The Netherlands. w.i.luining@amsterdamumc.nl.ORCID 0000-0003-4590-6589
André N VisDepartment of Urology, Amsterdam University Medical Center, VU university, location VUmc, De Boelelaan 1117, 1081 HV , Amsterdam, The Netherlands.
Maarten L DonswijkProstate Cancer Network the Netherlands, Amsterdam, The Netherlands.
Jose C C KoppesDepartment of Radiology & Nuclear Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Pim J van LeeuwenProstate Cancer Network the Netherlands, Amsterdam, The Netherlands.
Frederik OudshoornDepartment of Urology, Spaarne Gasthuis, Haarlem, The Netherlands.
Matthijs C F CysouwDepartment of Radiology & Nuclear Medicine, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Daniela E Oprea-LagerDepartment of Medical Imaging, Radboud University Medical Center, Nijmegen, The Netherlands.

Funding

Curium Pharma B.V. Curium Pharma B.V.
6 · The paper itself

Abstract

purposeThe current EAU-EANM-ESTRO-ESUR-ISUP-SIOG Guidelines recommend radiolabeled prostate-specific membrane antigen (PSMA), choline, or fluciclovine PET/CT at biochemical recurrence (BCR) of prostate cancer (PCa) after radical prostatectomy. While studies compared [68Ga]Ga-PSMA-11 and [18F]Fluciclovine, data on 18F-labelled PSMA-ligands versus [18F]Fluciclovine in patients with low prostate-specific antigen (PSA) levels (< 2 ng/mL) are limited. This study compared the detection rates of [18F]Fluciclovine and [18F]DCFPyL PET/CT in patients with BCR after robot-assisted radical prostatectomy (RARP). Secondary objectives included stratifying detection rates by PSA level, anatomical regions and assessing inter-observer agreement.

methodsIn this prospective, single-center study, patients with BCR (PSA 0.2-2.0 ng/mL) underwent both [18F]Fluciclovine and [18F]DCFPyL PET/CT within 15 days. Three blinded nuclear medicine experts independently reviewed all scans. Lesions were classified as positive or negative in predefined regions (i.e., prostate bed, pelvic and extra-pelvic lymph nodes, bone, and visceral). Discrepancies were resolved by consensus, defined as majority agreement (≥ 2/3 readers). Inter-observer agreement was assessed using Fleiss’ kappa.

resultsOverall scan positivity was 44% (22/50 patients) for [18F]DCFPyL PET/CT and 24% (12/50) for [18F]Fluciclovine PET/CT (p = 0.018). Detection rates increased with rising PSA levels for both tracers. Local recurrence was detected by both tracers in 16% (8/50) of patients. Metastatic disease detection rates for [18F]DCFPyL versus [18F]Fluciclovine were 22% vs. 8.0% for pelvic lymph nodes (p = 0.016), and 6.0% versus 2.0% for distant metastases (p = 0.50), respectively. Inter-observer agreement was moderate for both tracers (κ = 0.59 for [18F]DCFPyL and κ = 0.55 for [18F]Fluciclovine).

conclusionThis study demonstrated the superiority of [18F]DCFPyL over [18F]Fluciclovine in detecting pelvic lymph node metastases in patients presenting with BCR after RARP at low PSA levels. These findings suggest the potential of [18F]DCFPyL PET/CT to facilitate earlier and more personalized salvage treatment strategies.

Indexed as

Carboxylic AcidsCyclobutanesLysinePositron Emission Tomography Computed TomographyProstatectomyProstatic NeoplasmsRobotic Surgical ProceduresUreaAgedGlutaratesHumansMaleMiddle AgedProspective StudiesPyridinesRecurrenceCarboxylic AcidsCyclobutanesfluciclovine F-18GlutaratesLysinepiflufolastatPyridinesUrea[18F]DCFPyL[18F]FluciclovineBiochemical recurrenceFACBCPET/CTProstate cancer

Identifiers

PMID41762267
PMCPMC13197377

What OpenQuestion holds

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LicenceCC BY
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.