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Prediction of axillary nodal burden in patients with invasive lobular carcinoma using MRI

Authors :
Su Hyun Lee
Woo Kyung Moon
Su Min Ha
Jung Min Chang
Nariya Cho
Soo Yeon Kim
Eun Sil Kim
Yeon Soo Kim
Source :
Breast Cancer Research and Treatment. 186:463-473
Publication Year :
2021
Publisher :
Springer Science and Business Media LLC, 2021.

Abstract

To investigate clinical and imaging features associated with a high nodal burden (≥ 3 metastatic lymph nodes [LNs]) and compare diagnostic performance of US and MRI in patients with invasive lobular carcinoma (ILC) and invasive ductal carcinoma (IDC). Retrospective search revealed 239 patients with ILC and 999 with IDC who underwent preoperative US and MRI between January 2016 and June 2019. Patients with ILC were propensity-score-matched with patients with IDC. Univariate and multivariate logistic regression analyses were performed to determine factors associated with ≥ 3 metastatic LNs. 412 patients (206 ILC and 206 IDC) were evaluated. Of all patients with ILC, 27.2% (56/206) were node-positive and 7.8% (16/206) showed a high nodal burden. In multivariate analysis, the clinical N stage was the only independent factor associated with a high nodal burden in patients with IDC (odds ratio [OR] 6.24; 95% confidence interval [CI] 1.57–24.73; P = 0.009), but not in patients with ILC. Increased cortical thickness with loss of fatty hilum on US was associated with a high nodal burden in patients with ILC (OR 58.40; 95% CI 5.09–669.71; P = 0.001) and IDC (OR 24.14; 95% CI 3.52–165.37; P = 0.001), while suspicious LN findings at MRI were independently associated with a high nodal burden in ILC only (OR 13.94; 95% CI 2.61–74.39; P = 0.002). In patients with ILC, MRI findings of suspicious LNs were helpful to predict a high nodal disease burden.

Details

ISSN :
15737217 and 01676806
Volume :
186
Database :
OpenAIRE
Journal :
Breast Cancer Research and Treatment
Accession number :
edsair.doi.dedup.....808e8b47c2a5cbef61672fa19509215a
Full Text :
https://doi.org/10.1007/s10549-020-06056-9