MRI features of breast cancer immunophenotypes with a focus on luminal estrogen receptor low positive invasive carcinomas

• Published in: Scientific reports Vol. 14; no. 1; pp. 19305 - 10
• Main Authors: Tajima, Carla Chizuru, Arruda, Fernanda Pini Sapata Gonçalves, Mineli, Victor Chequer, Ferreira, Julianna Moura, Bettim, Barbara Beltrame, Osório, Cynthia Aparecida Bueno de Toledo, Sonagli, Marina, Bitencourt, Almir Galvão Vieira
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 20-08-2024; Nature Publishing Group; Nature Portfolio
• Subjects: 631/67; 692/308; Adult; Aged; Aged, 80 and over; Breast cancer; Breast carcinoma; Breast Neoplasms - diagnostic imaging; Breast Neoplasms - metabolism; Breast Neoplasms - pathology; Correlation analysis; ErbB-2 protein; Estrogen receptors; Estrogens; Female; Humanities and Social Sciences; Humans; Immunophenotyping; Invasiveness; Magnetic resonance imaging; Magnetic Resonance Imaging - methods; Middle Aged; multidisciplinary; Neoplasm Invasiveness; Receptor, ErbB-2 - metabolism; Receptors, Estrogen - metabolism; Regression analysis; Retrospective Studies; Science; Science (multidisciplinary); Statistical analysis; Triple-negative breast neoplasms; Tumors; Estrogen receptors; Triple-negative breast neoplasms; Breast cancer; Magnetic resonance imaging
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-69778-6

To compare the magnetic resonance imaging (MRI) features of different immunophenotypes of breast carcinoma of no special type (NST), with special attention to estrogen receptor (ER)-low-positive breast cancer. This retrospective, single-centre, Institutional Review Board (IRB)-approved study included 398 patients with invasive breast carcinoma. Breast carcinomas were classified as ER-low-positive when there was ER staining in 1–10% of tumour cells. Pretreatment MRI was reviewed to assess the tumour imaging features according to the 5th edition of the Breast Imaging Reporting and Data System (BI-RADS) lexicon. Of the 398 cases, 50 (12.6%) were luminal A, 191 (48.0%) were luminal B, 26 (6.5%) were luminal ER-low positive, 64 (16.1%) were HER2-overexpressing, and 67 (16.8%) were triple negative. Correlation analysis between MRI features and tumour immunophenotype showed statistically significant differences in mass shape, margins, internal enhancement and the delayed phase of the kinetic curve. An oval or round shape and rim enhancement were most frequently observed in triple-negative and luminal ER-low-positive tumours. Spiculated margins were most common in luminal A and luminal B tumours. A persistent kinetic curve was more frequent in luminal A tumours, while a washout curve was more common in the triple-negative, HER2-overexpressing and luminal ER-low-positive immunophenotypes. Multinomial regression analysis showed that luminal ER-low-positive tumours had similar results to triple-negative tumours for almost all variables. Luminal ER-low-positive tumours present with similar MRI findings to triple-negative tumours, which suggests that MRI can play a fundamental role in adequate radiopathological correlation and therapeutic planning in these patients.