Peritumoral edema in breast cancer at preoperative MRI: an interpretative study with histopathological review toward understanding tumor microenvironment

被引:54
作者
Park, Nora Jee-Young [1 ]
Jeong, Ji Yun [1 ]
Park, Ji Young [1 ]
Kim, Hye Jung [2 ]
Park, Chan Sub [3 ]
Lee, Jeeyeon [3 ]
Park, Ho Yong [3 ]
Jung, Jin Hyang [3 ]
Kim, Wan Wook [3 ]
Chae, Yee Soo [4 ]
Lee, Soo Jung [4 ]
Kim, Won Hwa [2 ]
机构
[1] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Pathol, Daegu, South Korea
[2] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Radiol, Daegu, South Korea
[3] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Surg, Daegu, South Korea
[4] Kyungpook Natl Univ, Chilgok Hosp, Sch Med, Dept Oncol Hematol, Daegu, South Korea
基金
新加坡国家研究基金会;
关键词
EXTRACELLULAR-MATRIX; TARGETING HYPOXIA; IMAGING FEATURES; PROGNOSIS; CARCINOMA; RECOMMENDATIONS;
D O I
10.1038/s41598-021-92283-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Peritumoral edema (PE) of breast cancer at T2-weighted MR images is considered a poor prognostic sign and may represent the microenvironment surrounding the tumor; however, its histopathological mechanism remains unclear. The purpose of the study was to identify and describe detailed histopathological characteristics associated with PE at preoperative breast MRI in breast cancer patients. This retrospective study included breast cancer patients who had undergone preoperative MRI and surgery between January 2011 and December 2012. Two radiologists determined the presence of PE in consensus based on the signal intensity surrounding the tumor at T2-weighted images. The following detailed histopathological characteristics were reviewed by two breast pathologists using four-tiered grades; lymphovascular invasion, vessel ectasia, stromal fibrosis, growth pattern, and tumor budding. Tumor necrosis and tumor infiltrating lymphocytes were assessed using a percent scale. Baseline clinicopathological characteristics, including age and histologic grade, were collected. The associations between detailed histopathologic characteristics and PE were examined using multivariable logistic regression with odds ratio (OR) calculation. A total of 136 women (median age, 49 +/- 9 years) were assessed; among them 34 (25.0%) had PE. After adjustment of baseline clinicopathological characteristics that were significantly associated with PE (age, T stage, N stage, histologic grade, and subtype, all Ps<0.05), lymphovascular invasion (P=0.009), vessel ectasia (P=0.021), stromal fibrosis (P=0.024), growth pattern (P=0.036), and tumor necrosis (P<0.001) were also associated with PE. In comparison with patients without PE, patients with PE were more likely to have a higher degree of lymphovascular invasion (OR, 2.9), vessel ectasia (OR, 3.3), stromal fibrosis (OR, 2.5), lesser degree of infiltrative growth pattern (OR, 0.4), and higher portion of tumor necrosis (OR, 1.4). PE of breast cancer at MRI is associated with detailed histopathological characteristics of lymphovascular invasion, vessel ectasia, stromal fibrosis, growth pattern, and tumor necrosis, suggesting a relevance for tumor microenvironment.
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页数:9
相关论文
共 33 条
[21]   Peritumoral edema as a biomarker of the aggressiveness of breast cancer: results of a retrospective study on a 3 T scanner [J].
Panzironi, Giovanna ;
Moffa, Giuliana ;
Galati, Francesca ;
Marzocca, Flaminia ;
Rizzo, Veronica ;
Pediconi, Federica .
BREAST CANCER RESEARCH AND TREATMENT, 2020, 181 (01) :53-60
[22]   The extracellular matrix modulates the hallmarks of cancer [J].
Pickup, Michael W. ;
Mouw, Janna K. ;
Weaver, Valerie M. .
EMBO REPORTS, 2014, 15 (12) :1243-1253
[23]   The Role of the Microenvironment in Mammary Gland Development and Cancer [J].
Polyak, Kornelia ;
Kalluri, Raghu .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2010, 2 (11) :a003244
[24]   Tumor Microenvironment of Metastasis and Risk of Distant Metastasis of Breast Cancer [J].
Rohan, Thomas E. ;
Xue, Xiaonan ;
Lin, Hung-Mo ;
D'Alfonso, Timothy M. ;
Ginter, Paula S. ;
Oktay, Maja H. ;
Robinson, Brian D. ;
Ginsberg, Mindy ;
Gertler, Frank B. ;
Glass, Andrew G. ;
Sparano, Joseph A. ;
Condeelis, John S. ;
Jones, Joan G. .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2014, 106 (08)
[25]  
ROSEN PP, 1983, PATHOL ANNU, V18, P215
[26]   The evaluation of tumor-infiltrating lymphocytes (TILs) in breast cancer: recommendations by an International TILs Working Group 2014 [J].
Salgado, R. ;
Denkert, C. ;
Demaria, S. ;
Sirtaine, N. ;
Klauschen, F. ;
Pruneri, G. ;
Wienert, S. ;
Van den Eynden, G. ;
Baehner, F. L. ;
Penault-Llorca, F. ;
Perez, E. A. ;
Thompson, E. A. ;
Symmans, W. F. ;
Richardson, A. L. ;
Brock, J. ;
Criscitiello, C. ;
Bailey, H. ;
Ignatiadis, M. ;
Floris, G. ;
Sparano, J. ;
Kos, Z. ;
Nielsen, T. ;
Rimm, D. L. ;
Allison, K. H. ;
Reis-Filho, J. S. ;
Loibl, S. ;
Sotiriou, C. ;
Viale, G. ;
Badve, S. ;
Adams, S. ;
Willard-Gallo, K. ;
Loi, S. .
ANNALS OF ONCOLOGY, 2015, 26 (02) :259-271
[27]   The hypoxic tumor microenvironment: A driving force for breast cancer progression [J].
Semenza, Gregg L. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (03) :382-391
[28]   MR imaging features associated with distant metastasis-free survival of patients with invasive breast cancer: a case-control study [J].
Song, Sung Eun ;
Shin, Sung Ui ;
Moon, Hyeong-Gon ;
Ryu, Han Suk ;
Kim, Kwangsoo ;
Moon, Woo Kyung .
BREAST CANCER RESEARCH AND TREATMENT, 2017, 162 (03) :559-569
[29]   The 2019 World Health Organization classification of tumours of the breast [J].
Tan, Puay Hoon ;
Ellis, Ian ;
Allison, Kimberly ;
Brogi, Edi ;
Fox, Stephen B. ;
Lakhani, Sunil ;
Lazar, Alexander J. ;
Morris, Elizabeth A. ;
Sahin, Aysegul ;
Salgado, Roberto ;
Sapino, Anna ;
Sasano, Hironobu ;
Schnitt, Stuart ;
Sotiriou, Christos ;
van Diest, Paul ;
White, Valerie A. ;
Lokuhetty, Dilani ;
Cree, Ian A. .
HISTOPATHOLOGY, 2020, 77 (02) :181-185
[30]   Focal breast edema associated with malignancy on T2-weighted images of breast MRI: peritumoral edema, prepectoral edema, and subcutaneous edema [J].
Uematsu, Takayoshi .
BREAST CANCER, 2015, 22 (01) :66-70