Evidence map›Paper›PMID 42566019›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Stage-dependent performance and molecular subtype-specific relapse patterns on same-session [18F]FDG PET/contrast-enhanced CT in breast cancer.

Agostino Chiaravalloti, Shyqyri Samarxhiu, Ilaria Portarena, Valeria Flaminio, Nicola D'Ascenzo, Orazio Schillaci, Gianluca Vanni

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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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5 · Who and what money

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7 authors.

Agostino ChiaravallotiDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Viale Montpellier 1, Rome, 00133, Italy. agostino.chiaravalloti@uniroma2.it.ORCID http://orcid.org/0000-0002-8017-8858
Shyqyri SamarxhiuDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Viale Montpellier 1, Rome, 00133, Italy.
Ilaria PortarenaMedical Oncology Unit, Fondazione PTV Policlinico Tor Vergata, Viale Oxford 81, Rome, 00133, Italy.
Valeria FlaminioMedical Oncology Unit, Fondazione PTV Policlinico Tor Vergata, Viale Oxford 81, Rome, 00133, Italy.
Nicola D'AscenzoDepartment of Electronic Engineering and Information Science, University of Science and Technology of China, Hefei, Anhui, China.
Orazio SchillaciDepartment of Biomedicine and Prevention, University of Rome Tor Vergata, Viale Montpellier 1, Rome, 00133, Italy.
Gianluca VanniBreast Unit, Department of Surgical Sciences, Fondazione PTV Policlinico Tor Vergata, University of Rome Tor Vergata, Rome, 00133, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo evaluate stage-dependent performance of same-session [18F]FDG PET/contrast-enhanced CT (PET/ceCT) for initial breast cancer staging and PET/ceCT-detected relapse patterns during follow-up.

methodsThis retrospective single-centre study included a primary staging cohort with one index PET/ceCT per patient and a longitudinal cohort of follow-up/restaging examinations. PET/ceCT-derived endpoints were assessed against clinically adjudicated reference standards established through multidisciplinary team review, pathology when available and follow-up imaging. SUVmax and ceCT lesion diameter were analysed as exploratory biomarkers.

resultsThe staging cohort included 116 patients. Baseline stage was evaluable in 106 patients: 65 had cN-positive disease, 9 had cT3-4 cN0 disease and 32 had cT1-2 cN0 disease. Overall nodal staging performance showed sensitivity 64.8%, specificity 88.9%, PPV 92.0%, NPV 56.1% and accuracy 72.9%. In cT3-4 and/or cN-positive disease, PET-positive nodal findings had a PPV of 100%. Baseline M-stage assessment was limited by the low number of clinically confirmed M1 cases. SUVmax correlated with Ki-67 (rho = 0.322, p = 0.003, q = 0.022). The longitudinal cohort included 176 patients and 429 examinations. In 311 adjudicated examinations, restaging performance for disease progression showed sensitivity 100%, specificity 93.5%, PPV 97.3%, NPV 100% and accuracy 98.1%. First confirmed relapse was multiorgan/multisystem in 48/82 patients and visceral-only in 15/82; visceral conversion occurred in 5/16 patients with initial bone-only or nodal/locoregional relapse.

conclusionSame-session [18F]FDG PET/ceCT showed greatest baseline utility in higher-risk breast cancer and was useful for longitudinal characterization of relapse phenotype and metastatic evolution.

Indexed as

[18F]FDG PET/CTBreast cancerContrast-enhanced CTMolecular subtypeRestagingStaging

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