Evidence map›Paper›PMID 42297930›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Diagnostic performance of

Kerim Şeker, Hüsnü Çağrı Genç, Tülay Koç, Mukaddes Yılmaz, Zekiye Hasbek

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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0citing papers 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

5 authors.

Kerim ŞekerDepartment of Nuclear Medicine, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Türkiye. kerimseker@cumhuriyet.edu.tr.ORCID 0000-0003-1683-1776
Hüsnü Çağrı GençDepartment of General Surgery, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Türkiye.
Tülay KoçDepartment of Medical Pathology, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Türkiye.
Mukaddes YılmazDepartment of Medical Oncology, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Türkiye.
Zekiye HasbekDepartment of Nuclear Medicine, Faculty of Medicine, Sivas Cumhuriyet University, Sivas, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to assess the diagnostic performance of MATERIALS AND

methodsWe retrospectively evaluated 279 treatment-naive female patients histopathologically diagnosed with Luminal A type breast cancer who underwent

resultsALN metastasis was confirmed in 152 (54.5%) patients. All quantitative parameters were significantly higher in the metastatic group (p < 0.001). While expert-based visual analysis showed 84.6% accuracy, axillary SUVmax (AUC: 0.881, 95% CI: 0.841-0.920) significantly outperformed visual assessment (AUC: 0.851, p = 0.031). At a cutoff of 0.93, axillary SUVmax yielded 83.6% sensitivity and 79.5% specificity. The Combined Model, integrating visual and quantitative data, achieved the highest diagnostic power (AUC: 0.889) and was statistically superior to axillary SUVmax alone (p = 0.022). The incorporation of quantitative data correctly reclassified 29% (NRI) of metastatic patients initially reported as false negatives in visual analysis and improved overall discrimination by 41.4% (IDI). DCA revealed that the combined model offered a higher net clinical benefit than standard surgical approaches within a 20-90% risk threshold range.

conclusionIn Luminal A-type breast cancer, objective quantitative 18F-FDG PET/CT parameters and their derived multiparametric models significantly exceed the diagnostic limitations of conventional visual assessment. By providing high net clinical benefit in the surgical decision-making process, the proposed combined model has the potential to serve as a valuable personalized decision support tool for the management of high-risk patients and the de-escalation of invasive surgery in low-risk cohorts.

Indexed as

Breast NeoplasmsFluorodeoxyglucose F18Lymphatic MetastasisPositron Emission Tomography Computed TomographyAdultAgedAxillaFemaleHumansMiddle AgedRetrospective StudiesFluorodeoxyglucose F1818F-FDG PET/CTAxillary lymph node metastasisDecision curve analysisIntegrated discrimination improvement (IDI)Luminal A breast cancerNet reclassification improvement (NRI)

Identifiers

PMID42297930
PMCPMC13526080

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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.