Evidence map›Paper›PMID 41721835›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Value of a repeat

Sonja Kirchhoff, Andreas Lederer, Theo Lorenzini, Michael Gammel, Daniel Sasse, Matthias Heck, Bernhard Haller, Wolfgang A Weber, Matthias Eiber, Isabel Rauscher

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.

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

10 authors.

Sonja KirchhoffDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Andreas LedererDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany. andreas.lederer@tum.de.ORCID 0009-0001-4314-531X
Theo LorenziniDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Michael GammelDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Daniel SasseDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Matthias HeckDepartment of Urology, School of Medicine, Technical University of Munich, Munich, Germany.
Bernhard HallerSchool of Medicine and Health, Institute of AI and Informatics in Medicine, TUM University Hospital, Technical University of Munich, Munich, Germany.
Wolfgang A WeberDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Matthias EiberDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.
Isabel RauscherDepartment of Nuclear Medicine, School of Medicine, Technical University of Munich, Ismaninger Straße 22, 81675, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo investigate the potential of a second 18F-flotufolastat positron emission tomography (PET) scan in patients with suspected biochemical recurrence (BCR) of prostate cancer (PCa) who had a previous negative 18F-flotufolastat PET, and to identify prostate-specific antigen (PSA) parameters influencing detection efficacy.

methodsOur retrospective analysis included data from patients who underwent second 18F-flotufolastat PET between 2019 and 2024, following negative 18F-flotufolastat PET for suspected BCR of PCa (PSA ≥ 0.2 ng/mL) after radical prostatectomy. Two board-certified experts classified 18F-flotufolastat-avid lesions per miTNM categories. Patient-level detection rates were stratified by: pre-PET scan PSA; absolute/relative difference in PSA (ΔPSA) between negative first and second PET; PSA velocity (PSAvel); PSA doubling time (PSAdt). Receiver operating characteristic (ROC) curve analyses were performed.

resultsOf 101 patients (median age = 70 years; median PSA = 0.79 ng/mL), 58 (57%) had a positive second 18F-flotufolastat scan. Detection rates increased with PSA level, ΔPSA, PSAvel, and PSAdt. Differences in PSA level, ΔPSA, PSAvel, and PSAdt between groups with/without suspicious 18F-flotufolastat uptake were statistically significant (p < 0.05). Cut-offs for statistically optimal trade-off between negative and positive second PET (ROC analyses) were: PSA level > 0.82 ng/mL; absolute ΔPSA > 0.50 ng/mL; relative ΔPSA > + 100%; PSAvel > 0.30 ng/mL/y; PSAdt ≤ 17 months.

conclusionIn over half of patients presenting with BCR after radical prostatectomy and an initial negative 18F-flotufolastat PET, second 18F-flotufolastat PET identified recurrent lesions. PSA level at time of second PET, absolute/relative ΔPSA, PSAvel, and PSAdt influenced scan positivity.

Indexed as

Fluorine RadioisotopesHydroxamic AcidsNeoplasm Recurrence, LocalPositron-Emission TomographyProstatectomyProstatic NeoplasmsAgedHumansMaleMiddle AgedProstate-Specific AntigenRecurrenceRetrospective StudiesFluorine-18Fluorine RadioisotopesHydroxamic AcidsProstate-Specific AntigenBiochemical recurrenceHybrid imagingPositron emission tomographyProstate cancerProstate‐specific membrane antigen

Identifiers

PMID41721835
PMCPMC13249659

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Registered trials

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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.