Evidence map›Paper›PMID 41191096›Full record

ArticleEuropean journal of nuclear medicine and molecular imaging2026

Integrating PET/CT-derived heterogeneity indices and composite risk scores improves prognostic stratification in breast cancer.

Mehmet Tarık Tatoğlu, İlker Nihat Ökten, Ebru İbişoğlu, Tuçe Söylemez Akkurt, Esra Tozan, Ferda Yerdelen Tatoğlu, Hatice Uslu

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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. Cited by 2 papers.

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2citing 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

2 citing papers in PubMed.

  1. Prognostic value and diagnostic performance of nectin-4-targeted [European journal of nuclear medicine and molecular imaging · 2026
    Article
  2. A pretreatmentTranslational cancer research · 2026
    Article
4 · The record

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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

7 authors.

Mehmet Tarık TatoğluDepartment of Nuclear Medicine, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye. m.tatoglu@saglik.gov.tr.ORCID 0000-0002-1680-4973
İlker Nihat ÖktenDepartment of Medical Oncology, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye.ORCID 0000-0003-2360-3392
Ebru İbişoğluDepartment of Nuclear Medicine, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye.ORCID 0000-0002-9132-9092
Tuçe Söylemez AkkurtDepartment of Pathology, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye.ORCID 0000-0003-3030-7030
Esra TozanDepartment of Radiology, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye.ORCID 0009-0003-8324-8908
Ferda Yerdelen TatoğluDepartment of Econometrics, Faculty of Economics, Istanbul University, Fatih, Istanbul, Türkiye.ORCID 0000-0002-7365-3649
Hatice UsluDepartment of Nuclear Medicine, Goztepe Prof. Dr. Suleyman Yalcin City Hospital, Kadikoy, Istanbul, Türkiye.ORCID 0000-0003-0456-261X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aimed to assess the prognostic significance of novel and established intratumoral heterogeneity indices (HIs) derived from

methodsWe retrospectively evaluated 135 BC patients who underwent [18 F]FDG PET/CT for pretreatment staging. Metabolic and volumetric data of primary tumors obtained from [18 F]FDG PET/CT images, such as the maximum, mean, peak, and minimum standardized uptake values (SUVmax, SUVmean, SUVpeak, and SUVmin), the SUV corrected for lean body mass (LBM) calculated by James's and Janmahasatian's methods (SULmax, SULmean, SULpeak, and SULmin), metabolic tumor volume (MTV), and total lesion glycolysis (TLG), and two predefined and seven novel HIs were compared between molecular subtypes via the Kruskal-Wallis (KW) test. All relevant HI, PET/CT-derived metrics, and clinical, pathological, and metastatic variables were included in the cross-validated LASSO regression models to estimate the overall survival (OS) endpoints for 1, 2, 3, 4, and 5 years.

resultsSignificant differences were observed between molecular subtypes for SUVmax, SUVpeak, TLG_40, and HI5 (Janma/James) (p < 0.05), with the highest values in the HER2-enriched and triple-negative (TNBC) subtypes. CRS, which combines clinical factors, metastatic status, PET/CT-derived metrics, and HI, demonstrated robust discrimination of OS (area under the curve [AUC]: 0.79-0.91) and outperformed single-parameter models. Among the heterogeneity indices, HI2 and HI4 showed the strongest independent predictions of OS at multiple time points, although a combination of multiple parameters was required for optimal prognostic accuracy.

conclusionCRS, which integrates imaging-derived heterogeneity and metabolic and clinical data, offers improved OS prediction and individualized risk stratification in BC patients.

Indexed as

Breast NeoplasmsPositron Emission Tomography Computed TomographyAdultAgedAged, 80 and overFemaleFluorodeoxyglucose F18HumansMiddle AgedPrognosisRetrospective StudiesRisk AssessmentFluorodeoxyglucose F18[18F]FDG PET/CTBreast cancerHeterogeneity indicesTumoral heterogeneity

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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.