Evidence map›Paper›PMID 42704038›Full record

ArticleRadiology and oncology2026

Breast DCE-MRI morphological features and semi-quantitative parameters associated with upgrade to invasive carcinoma in biopsyproven DCIS.

Vladimir Urban, Zorica Milosevic, Zoran Bukumiric, Katarina Obradovic, Nina Adzic, Dragana Pavlovic-Stankovic, Ivana Petkovic, Ivana Sovic, Irena Jovanic, Igor Spurnic

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Article in Radiology and oncology, 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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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Vladimir Urban1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Zorica Milosevic2School of Medicine, University of Belgrade, Belgrade, Serbia.
Zoran Bukumiric2School of Medicine, University of Belgrade, Belgrade, Serbia.
Katarina Obradovic1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Nina Adzic1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Dragana Pavlovic-Stankovic1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Ivana Petkovic1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Ivana Sovic1Department of Diagnostic Radiology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Irena Jovanic4Department of Pathology, Institute for Oncology and Radiology of Serbia, Belgrade, Serbia.
Igor Spurnic2School of Medicine, University of Belgrade, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe aim of this study was to identify imaging predictors of upgrade to invasive carcinoma (IC) in patients with biopsy-proven ductal carcinoma PATIENTS AND

methodsNinety consecutive patients with biopsy-proven DCIS who had positive findings on standard full-protocol breast DCE-MRI and subsequently underwent surgical excision with final postoperative histopathological diagnosis were included. Patients with final postoperative IC were compared with those without IC. Morphological features (lesion type, size, multifocality/multicentricity, T2-weighted (T2W) and turbo inversion recovery magnitude [TIRM] characteristics) and semi-quantitative parameters (wash-in, peak enhancement, delayed phase of the timeintensity curve [TIC], time to peak [TTP], and positive enhancement integral [PEI]) were analyzed.

resultsFifty-five patients (61.1%) had no IC, while 35 patients (38.9%) had IC on final histopathology. Patients with IC more frequently demonstrated non-mass enhancement (NME) combined with a mass, larger lesion size, multifocal or multicentric disease, T2W/TIRM hyperintensity, fast wash-in, higher peak enhancement, plateau and washout TIC patterns, higher PEI, and shorter TTP. Multivariate analysis identified NME combined with a mass, delayed-phase TIC characteristics, and TIRM hyperintensity as independent predictors of IC.

conclusionsOur study confirmed that prediction models incorporating breast DCE-MRI morphological features and semi-quantitative parameters can stratify patients with biopsy-proven DCIS by their probability of upgrade to IC. TIRM hyperintensity emerged as one of three independent predictors of IC and, to the best of our knowledge, has not been previously reported in this context.

Indexed as

Breast NeoplasmsCarcinoma, Ductal, BreastCarcinoma, Intraductal, NoninfiltratingDynamic Contrast Enhanced Magnetic Resonance ImagingAdultAgedAged, 80 and overBiopsyContrast MediaFemaleHumansMiddle AgedNeoplasm InvasivenessRetrospective StudiesContrast Mediabreast biopsybreast MRIDCISinvasive carcinomasemi-quantitativeupgrade

Identifiers

PMID42704038
PMCPMC13548675

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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.