Korean J Radiol.  2017 Feb;18(1):238-248. 10.3348/kjr.2017.18.1.238.

Estimation of T2* Relaxation Time of Breast Cancer: Correlation with Clinical, Imaging and Pathological Features

Affiliations
  • 1Department of Radiology, Kyung Hee University Hospital, College of Medicine, Kyung Hee University, Seoul 02447, Korea.
  • 2Department of Radiology, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul 05278, Korea. oddie2@naver.com
  • 3Department of Pathology, Kyung Hee University Hospital at Gangdong, College of Medicine, Kyung Hee University, Seoul 05278, Korea.

Abstract


OBJECTIVE
The purpose of this study was to estimate the T2* relaxation time in breast cancer, and to evaluate the association between the T2* value with clinical-imaging-pathological features of breast cancer.
MATERIALS AND METHODS
Between January 2011 and July 2013, 107 consecutive women with 107 breast cancers underwent multi-echo T2*-weighted imaging on a 3T clinical magnetic resonance imaging system. The Student's t test and one-way analysis of variance were used to compare the T2* values of cancer for different groups, based on the clinical-imaging-pathological features. In addition, multiple linear regression analysis was performed to find independent predictive factors associated with the T2* values.
RESULTS
Of the 107 breast cancers, 92 were invasive and 15 were ductal carcinoma in situ (DCIS). The mean T2* value of invasive cancers was significantly longer than that of DCIS (p = 0.029). Signal intensity on T2-weighted imaging (T2WI) and histologic grade of invasive breast cancers showed significant correlation with T2* relaxation time in univariate and multivariate analysis. Breast cancer groups with higher signal intensity on T2WI showed longer T2* relaxation time (p = 0.005). Cancer groups with higher histologic grade showed longer T2* relaxation time (p = 0.017).
CONCLUSION
The T2* value is significantly longer in invasive cancer than in DCIS. In invasive cancers, T2* relaxation time is significantly longer in higher histologic grades and high signal intensity on T2WI. Based on these preliminary data, quantitative T2* mapping has the potential to be useful in the characterization of breast cancer.

Keyword

Breast cancer; T2*; Relaxation time; Susceptibility; Breast; Magnetic resonance imaging

MeSH Terms

Adult
Breast Neoplasms/*diagnosis/diagnostic imaging/pathology
Carcinoma, Intraductal, Noninfiltrating/diagnosis/diagnostic imaging/pathology
Female
Humans
Linear Models
Magnetic Resonance Imaging
Mammography
Middle Aged
Neoplasm Invasiveness

Figure

  • Fig. 1 T2* relaxation time mapping from 55-year-old woman with ductal carcinoma in situ. A. Sagittal contrast-enhanced T1-weighted image shows heterogeneous non-mass enhancement left breast. Region of interest of breast cancer (red) and normal parenchyma (green) was manually outlined and later copied onto T2* map. B. Signal intensity changes on MR images were used to calculate intrinsic T2* relaxivity. R2* values were found by taking negative of linear slope of signal intensity plotted against echo time (TE) for each voxel, of which the gradient is–R2* (measured in 1/ms). Reciprocal of R2* was T2*. C. T2* map shows similar T2* value in breast cancer compared with surrounding glandular tissue. Mean T2* value of breast cancer and parenchyma were 22.7 and 18.9 ms, respectively. D. On coronal T2-weighted image, cancer in left breast was not prominent and classified as iso- signal intensity compared with breast parenchyma.

  • Fig. 2 Representative case in 44-year-old woman with high-grade invasive ductal carcinoma. A. Sagittal contrast-enhanced T1-weighted image shows heterogeneous enhancing mass (arrow) in right breast middle portion. B. T2* map shows increased T2* value in breast cancer (arrow) compared with surrounding glandular tissue. Mean T2* value of breast cancer and normal parenchyma were 50.6 and 35.2 ms, respectively. C. Coronal T2-weighted image shows high signal intensity mass accompanying peritumoral edema in right breast (arrows), which was classified as very high signal intensity. D. Histopathological image shows high cellularity, no tubule formation, and little collagen matrix (hematoxylin and eosin stain, × 400).

  • Fig. 3 Representative case in 72-year-old woman with low-grade invasive ductal carcinoma. A. Sagittal contrast-enhanced T1-weighted image shows posterior located enhancing mass (arrow). B. T2* map shows similar T2* value in breast cancer (arrows) compared with surrounding glandular tissue. Mean T2* value of breast cancer and normal parenchyma were 23.4 and 23.4 ms, respectively. C. Coronal T2-weighted image shows mass in left breast which is located posterior to breast parenchyma and has slightly higher signal intensity compared to breast parenchyma (arrows). D. Histopathological image shows increased tubule and gland formation, and rich collagen matrix (hematoxylin and eosin stain, × 200).


Cited by  1 articles

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