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Triple-negative breast carcinoma: Heterogeneity in immunophenotypes and pharmacokinetic behavior

Authors :
F.J. Andreu Navarro
J. H. del Riego Ferrari
M. Lluïsa Baré
J. Planas Roquerols
M. Vilagran Fraguell
M. Sentís Crivillé
E. Dalmau Portulàs
Source :
Radiología (English Edition). 58:55-63
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Objectives To evaluate the morphokinetic, pharmacokinetic, and diffusion characteristics of triple-negative breast cancers on magnetic resonance (MR) imaging and to analyze whether there is a relation between these parameters and the time to progression. Material and methods This was a retrospective observational study of a consecutive series of 100 patients with histologically confirmed triple-negative breast cancer studied at our center between January 2005 and December 2010. We reviewed the findings on MR locoregional extension studies, the histological findings, and the follow-up of patients until August 2014. Results The most common MR findings for these tumors were a rounded mass (47.3%), well-defined borders (53.7%), ring enhancement (46.2%), type 3 curves (50.5%), hyperintensity within the tumor on T2-weighted sequences, high ADC values (1.04 × 10 −3 mm 2 /s), and increased capillary permeability (Kep) (0.94 min −1 ). No significant association was observed between the morphokinetic or pharmacokinetic characteristics and the time to progression. The in situ component in the surgical specimens was high, although its expression was low. During follow-up, 25% of patients had metastases, with a predilection for the visceral organs, and survival was low. Conclusion Tumors with the triple-negative phenotype mostly presented in MR as rounded tumors with well-defined borders and ring enhancement. We found no significant association between the morphokinetic or pharmacokinetic characteristics and the time to progression.

Details

ISSN :
21735107
Volume :
58
Database :
OpenAIRE
Journal :
Radiología (English Edition)
Accession number :
edsair.doi...........b66f1ead151f927268f0e87498ce06c2
Full Text :
https://doi.org/10.1016/j.rxeng.2015.12.002