Imaging and histologic prognostic factors in triple-negative breast cancer and carcinoma in situ as a prognostic factor

被引:0
|
作者
Sebastian Sebastian, C. [1 ]
Garcia Mur, C. [1 ]
Cruz Ciria, S. [1 ]
Rosero Cuesta, D. S. [2 ]
Gros Baneres, B. [3 ]
机构
[1] Hosp Univ Miguel Servet, Serv Radiodiagnost, Zaragoza, Spain
[2] Hosp Univ Miguel Servet, Serv Anat Patol, Zaragoza, Spain
[3] Hosp Univ Miguel Servet, Serv Urgencias, Zaragoza, Spain
来源
RADIOLOGIA | 2016年 / 58卷 / 04期
关键词
Breast cancer; Triple-negative tumors; Carcinoma in situ; Prognostic markers; Recurrence; Magnetic resonance imaging; Diffusion; Perfusion; ki67; p53;
D O I
10.1016/j.rx.2.016.07.004
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objectives: To analyze what factors in magnetic resonance imaging (MRI) and histological study of triple-negative breast cancers are related to tumor recurrence and to shorter disease-free survival. To analyze survival and recurrence in function of the presence of an in situ component. Material and methods: This was a retrospective study of MRI staging examinations in 122 women with triple-negative breast cancer done from 2007 through 2014. In the MRI, we evaluated morphological variables (size, margins, morphology, internal signal in T2-weighted sequences) and dynamic variables (perfusion and diffusion). In the histological study, we evaluated Ki67, p53, CK5/6, nuclear grade, and Scarff-Bloom grade, as well as the presence of an in situ component and tumor grade (high grade or not high grade). We compared the variables between patients with tumor recurrence and those without, and we conducted a survival analysis. Results: Non-nodular enhancement was more common in patients with tumor recurrence (p = 0.038) and was associated with shorter disease-free survival (p= 0.023). Neither diffusion restriction (p = 0.079) nor ki67 (p = 0.052) was associated with a worse prognosis. An in situ component was detected in 44% of triple-negative tumors, and a greater proportion of patients in the group with tumor recurrence had an in situ component; however, the presence of an in situ component was not associated with shorter survival (p = 0.185). Conclusion: Non-nodular enhancement was associated with a worse prognosis. Diffusion restriction, ki67, and the presence of an in situ component were not associated with shorter disease-free survival. (C) 2016 SERAM. Published by Elsevier Espana, S.L.U. All rights reserved.
引用
收藏
页码:283 / 293
页数:11
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