TY - JOUR
T1 - Apparent diffusion coefficient in estrogen receptor-positive invasive ductal breast carcinoma
T2 - Correlations with tumor-stroma ratio
AU - Ko, Eun Sook
AU - Han, Boo Kyung
AU - Kim, Rock Bum
AU - Cho, Eun Yoon
AU - Ahn, Soomin
AU - Nam, Seok Jin
AU - Ko, Eun Young
AU - Shin, Jung Hee
AU - Hahn, Soo Yeon
PY - 2014/4
Y1 - 2014/4
N2 - Purpose: To determine whether apparent diffusion coefficient (ADC) values vary according to tumor-stroma ratio, dominant stroma type, or presence of central fibrosis in estrogen receptor-positive breast cancer. Materials and Methods: Institutional review board approval was obtained, and patient consent was waived. Sixty-one patients with estrogen receptor-positive invasive ductal carcinoma-not otherwise specified who underwent breast magnetic resonance (MR) imaging with diffusion-weighted (DW) imaging were included in this study. The ADC values of the lesions were measured. Two pathologists evaluated the tumor-stroma ratio, dominant stroma type (collagen, fibroblast, lymphocyte), and central fibrosis. Detectability on DW images was compared between the two groups according to the tumor-stroma ratio (stroma rich or stroma poor). Mean ADC values were retrospectively compared with the tumor-stroma ratio, dominant stroma type, and presence of a central fibrosis. Multiple linear regression analysis was performed to determine variables independently associated with ADC. Results: On DW images, detectability was not significantly different between stroma-rich and stroma-poor groups (P = .244). ADC values were significantly lower in the stroma-poor group (P < .001). The mean ADC values in the collagen-dominant type were lower than in fibroblast-dominant or lymphocyte-dominant types (P = .021). In multiple linear regression analysis, tumor-stroma ratio (P = .007), tumor size (P = .007), and dominant stroma type (collagen dominant, P = .029) were independently correlated with ADC. Conclusion: In estrogen receptor-positive breast cancers, ADC values showed significant differences according to the tumorstroma ratio and dominant stroma type.
AB - Purpose: To determine whether apparent diffusion coefficient (ADC) values vary according to tumor-stroma ratio, dominant stroma type, or presence of central fibrosis in estrogen receptor-positive breast cancer. Materials and Methods: Institutional review board approval was obtained, and patient consent was waived. Sixty-one patients with estrogen receptor-positive invasive ductal carcinoma-not otherwise specified who underwent breast magnetic resonance (MR) imaging with diffusion-weighted (DW) imaging were included in this study. The ADC values of the lesions were measured. Two pathologists evaluated the tumor-stroma ratio, dominant stroma type (collagen, fibroblast, lymphocyte), and central fibrosis. Detectability on DW images was compared between the two groups according to the tumor-stroma ratio (stroma rich or stroma poor). Mean ADC values were retrospectively compared with the tumor-stroma ratio, dominant stroma type, and presence of a central fibrosis. Multiple linear regression analysis was performed to determine variables independently associated with ADC. Results: On DW images, detectability was not significantly different between stroma-rich and stroma-poor groups (P = .244). ADC values were significantly lower in the stroma-poor group (P < .001). The mean ADC values in the collagen-dominant type were lower than in fibroblast-dominant or lymphocyte-dominant types (P = .021). In multiple linear regression analysis, tumor-stroma ratio (P = .007), tumor size (P = .007), and dominant stroma type (collagen dominant, P = .029) were independently correlated with ADC. Conclusion: In estrogen receptor-positive breast cancers, ADC values showed significant differences according to the tumorstroma ratio and dominant stroma type.
UR - https://www.scopus.com/pages/publications/84896937622
U2 - 10.1148/radiol.13131073
DO - 10.1148/radiol.13131073
M3 - Article
C2 - 24475830
AN - SCOPUS:84896937622
SN - 0033-8419
VL - 271
SP - 30
EP - 37
JO - Radiology
JF - Radiology
IS - 1
ER -