- Open Access
Role of perfusion parameters on DCE-MRI and ADC values on DWMRI for invasive ductal carcinoma at 3.0 Tesla
© The Author(s). 2018
- Received: 19 April 2018
- Accepted: 30 November 2018
- Published: 21 December 2018
The value of apparent diffusion coefficient (ADC) values and quantitative parameters (Ktrans, Kep, Ve) in detecting prognostic factor at 3.0 Tesla remains unclear, especially in predicting prognosis of breast cancer.
A total of 151 patients with IDC underwent breast DCE-MRI and DWI-MRI at 3.0 Tesla following surgery. The ADC values were acquired with b values of 0 and 1000 s/mm2. The relationship between ADC values or DCE-MRI quantitative parameters and size, histologic grade (HG), lymph node metastasis (LNM), ER, PR, and Ki67 was evaluated. The predictive values of ADC, Ktrans, Kep, and Ve to prognosis of IDC were assessed.
ADC value was positively related to size (P = 0.04) and HER2 (P = 0.046) expression and negatively related to ER (P = 0.012) and PR (P < 0.001) expression. Ktrans value has positive correlation with size (P < 0.001), HG (P < 0.001), LNM (P < 0.001), HER2 (P = 0.007), and Ki67 (P < 0.001) expression and negative correlation with ER (P < 0.001) and PR (P < 0.001) expression. Kep value was positively related to size (P < 0.001) and negatively related to ER (P < 0.001) and PR (P < 0.001) expression. Ve value was negatively related to HER2 expression (P = 0.004). The Cox hazard ratio (HR) of ADC, Ktrans, Kep, and Ve values on survival was 5.26 (P = 0.093), 1.081 (P = 0.002), 1.006 (P = 0.941), and 0.883 (P = 0.926), respectively.
Ktrans value was a best predictive indicator of HG, LNM, ER, PR, and Ki67 expression, and ADC value was the best predictive indicator of HER2. Preoperative use of the 3.0 Tesla could provide important information to determine the optimal treatment plan.
- Diffusion-weighted MRI
- Magnetic resonance imaging
- Invasive ductal carcinoma
- Breast cancer
Breast cancer is a highly heterogeneous disease with multiple biological subtypes that are distinguished by different clinical, pathological, and molecular characteristics, treatment measures, and prognosis . The morphological and cytological features of the tumor are closely related to the degree of malignancy of the tumor. Multi-gene expression analysis demonstrated that this clinical feature of breast cancer is a result of potential gene expression or inhibition . Currently recognized cytokines that evaluate the therapeutic effect and prognosis of breast cancer include estrogen receptor (ER), progesterone (PR), human epidermal growth factor receptor (2), human epidermal growth factor receptor-2 (HER-2), and nucleus-associated antigen Ki-67, which play a synergistic role in the development of breast cancer via influencing the occurrence, development, and prognosis of breast cancer [3, 4].
Early diagnosis of breast cancer plays an important role in the choice of treatment regimen and the prognosis of the disease . Dynamic contrast-enhanced magnetic resonance imaging (DCE-MRl) is a noninvasive diagnosis of assessing the internal microenvironment of the tumor in recent years . The imaging technique can reflect the characteristics of blood flow, microvascular permeability, vascular density, tissue oxygen concentration, and even tissue metabolic level [6, 7]. Studies had confirmed that DCE-MRI can evaluate and predict the clinical efficacy and prognosis of bladder cancer, bone tumor, and breast cancer [8, 9].
Currently, magnetic resonance imaging has become one of the indispensable means of examination for breast disease and breast-conserving surgery . In addition, magnetic resonance imaging can also be used to assess tumor functional changes through special examinations such as diffusion-weighted imaging (DWI) and hydrogen proton resonance spectroscopy (1H-MRS) [11, 12]. Furthermore, it is important to evaluate the number of tumors, the extent of invasion of lesions, and lymph node metastasis (LNM) and TNM staging in patients with neoadjuvant chemotherapy and post-chemotherapy evaluation [13, 14]. In particular, DWI is capable of imaging the microscopic diffusion of water molecules, which can identify the function and metabolic state of tumor tissues and quantify the dispersion of water molecules through ADC values .
The previous investigations had reported the average values of ADC in malignant and benign breast tumors and the threshold values of ADC that distinguished malignancies from benign lesions [15–17]. However, there only were few reports of applications of both DWI and DCE-MRl on the invasive ductal carcinoma (IDC) evaluation. The aim of this study was to assess the correlations between parameters of DWI and DCE-MRl in IDC of the breast and prognosis or prognostic factors, such as tumor size, histologic grade, lymph nodes metastasis (LNM), estrogen receptor (ER), progesterone receptor (PR), HER2 (c-erb-2), and Ki-67.
This is a prospective study that was approved by our hospital institutional review board, and informed consent was obtained from all patients.
A total of 207 patients with breast cancer who were admitted to our hospital from March 2010 to April 2012 were all female and aged from 31 to 77 years with an average of 52 ± 10.3 years. Among them, 151 patients who were diagnosed with histopathological IDC of the breast by pathological diagnosis postoperatively were enrolled in this study. There were 56 patients who had final diagnoses of other breast cancers, including ductal carcinoma in situ (DCIS) (n = 28), invasive lobular carcinoma (n = 5), intraductal papillary carcinoma (n = 4), and DCIS with microinvasion (n = 19), excluded. The average age of the 151 patients enrolled in this study was 51.7 ± 10.6. In addition to surgical treatment, information on other treatment methods for patients with IDC, including surgical methods, chemotherapy, and endocrine therapy, was collected.
The breast MRI studies were performed on a MAGNETOM Verio 3.0 Tesla (T) scanner (Siemens Medical Solutions, Germany) using a dedicated 16-channel breast-specific phased array surface coil with patients in the prone position. Parameters for several sequences were listed as follows: T2-weighted imaging (T2WI): TR/TE, 4000/70 ms; slice thickness, 5 mm, 0.5 mm gap; field of view (FOV), 340 × 340; matrix, 448 × 448; NEX,1. T1WI (FLASH-3D): TR/TE, 3.6/2.1 ms; slice thickness, 1.2 mm, 0.2 mm gap; FOV, 340 × 340; matrix, 448 × 380; flip angle, 10°; NEX,0.7. EPI-DWI: TR/TE, 8300/85 ms; slice thickness, 4 mm, 2 mm gap; FOV, 360 × 147; matrix, 220 × 220; NEX,3; performed by fat suppression technology with b values of 0 and 1000 s/mm2. DCE-MRI was performed by the following parameters: TR/TE, 4.5/1.6 ms; flip angle, 10°; slice thickness,1 mm, 0.2 mm gap; matrix, 448 × 344; FOV, 340 × 340; NEX, 1. The first phase scan was conducted before the contrast agent was injected. After 25 s, Gd-DTPA (0.1–0.15 mmol/kg) was injected intravenously at a flow rate of 3.0 ml/s with a high-pressure syringe, followed by administration of a saline flush. The acquisition time was 487 s (77 s per dynamic sequence).
All images were processed on a Siemens post-processing workstation. Three imaging diagnosticians were randomly assigned to read and analyze the MRI information of patients, and they were blinded from histological results. The inconsistencies in the results are agreed upon by consensus.
The quantitative DCE-MRI parameters were calculated by non-linear least squares method using the two-compartment model of Tofts et al. in the German Siemens MRI Workstation 4D tissue software . Quantitative DCE-MRI parameters include volume transfer constant (Ktrans), rate constant (Kep), and extravascular space (Ve). The maximum diameter of the lesion was selected as the region of interest (ROI), and the average value was obtained from three times determinations with avoiding the liquefaction, necrosis, and bleeding area of tumor tissue and other features. The size of the tumor and the enhanced morphology were obtained by enhancing images. According to the different enhanced morphologies of breast cancer, tumors were divided into enhanced lump group and non-lump enhanced group.
By using Mean Curve software from Siemens post-processing workstation, the lesion with higher signal intensity was selected as the region of interest (ROI) to draw time-signal intensity curve (TIC). Two different areas of the lesion were selected, and three different ROIs were taken for each area. The ROI sizes ranged from 15.0 to 420.6 mm2.
For measurements of ADC values, three ROIs were selected within the main lesions and mean values were calculated with B = 0, 1000 s/mm2 as the apparent diffusion coefficient of the b value. All measurements were performed independently by two mammography diagnostic specialists with at least 4 years of experience.
Histological grading of IDC was performed based on nuclear polymorphic tubular structures and mitotic counts according to the modified criteria of Bloom and Richardson . Historical analysis was performed by surgically resected specimens. A score of 3–5, 6–7, and 8–9 were considered grade I, grade II, and grade III, respectively. According to the International Union Against Cancer (UICC) TNM staging system, breast cancer size was divided into three groups: maximum diameter of the tumor < 2 cm (size 1), 2 cm–5 cm (size 2), and ≥ 5 cm (size 3). The lymph node metastasis was assessed by routine staining. Immunohistochemistry of ER, PR, Ki-67, and HER2 (c-erbB-2) was analyzed as molecular markers. By routine staining procedures, the case with more than 10% of cancer cells with nuclear staining was regarded as ER, PR, or Ki-67 positivity. Scores of 0 (negative), were considered negative for expression of proteins, scores of 1+ and 2+ (moderate) were regarded as positive for expression of proteins, and scores of 3+ (strong) was considered positive for over-expression of proteins.
Follow-up is performed every 2 months for 60 months. The overall survival is defined as the time from diagnosis of any cause to death.
General information of patients (n = 151)
No. of cases
< 2 cm
1.04 ± 0.23
12.00 ± 0.65
0.64 ± 1.41
0.19 ± 0.28
1.16 ± 0.25
18.15 ± 8.50
2.90 ± 6.59
0.20 ± 0.37
> 5 cm
1.09 ± 0.15
15.98 ± 8.12
1.58 ± 1.63
0.09 ± 0.12
1.10 ± 0.24
13.96 ± 7.32
1.73 ± 4.51
0.18 ± 0.29
1.13 ± 0.23
21.78 ± 7.57
2.52 ± 6.24
0.18 ± 0.39
1.00 ± 0.27
7.73 ± 4.89
2.99 ± 3.76
0.28 ± 0.34
1.15 ± 0.24
15.21 ± 7.99
1.47 ± 4.60
0.14 ± 0.27
1.10 ± 0.23
19.51 ± 6.94
2.16 ± 5.76
0.21 ± 0.36
1.09 ± 0.28
13.96 ± 8.30
2.61 ± 6.37
0.24 ± 0.39
1.13 ± 0.18
18.43 ± 7.22
1.11 ± 2.26
0.11 ± 0.17
1.15 ± 0.25
19.02 ± 6.48
2.00 ± 5.77
0.20 ± 0.36
1.12 ± 0.29
16.76 ± 10.71
0.97 ± 1.76
0.13 ± 0.26
1.06 ± 0.18
12.15 ± 6.11
2.49 ± 5.50
0.21 ± 0.31
1.16 ± 0.28
19.22 ± 6.85
2.98 ± 6.92
0.21 ± 0.38
1.10 ± 0.23
13.31 ± 9.04
1.83 ± 2.73
0.25 ± 0.31
1.02 ± 0.12
13.33 ± 6.86
0.05 ± 0.12
0.05 ± 0.10
1.02 ± 0.24
14.28 ± 8.94
3.91 ± 7.17
0.33 ± 0.42
1.12 ± 0.18
16.60 ± 7.19
0.53 ± 1.09
0.06 ± 0.12
1.29 ± 0.27
18.55 ± 7.35
0.40 ± 0.78
0.11 ± 0.19
1.12 ± 0.15
8.60 ± 4.80
6.18 ± 8.19
0.29 ± 0.36
1.09 ± 0.25
15.49 ± 6.75
0.63 ± 1.30
0.13 ± 0.24
1.15 ± 0.26
20.61 ± 9.36
2.92 ± 6.90
0.26 ± 0.42
1.10 ± 0.22
16.89 ± 8.12
1.93 ± 5.22
0.19 ± 0.33
1.17 ± 0.33
10.31 ± 5.45
1.96 ± 3.48
0.16 ± 0.26
1.04 ± 0.28
9.59 ± 5.52
0.96 ± 1.81
0.18 ± 0.31
1.12 ± 0.24
16.58 ± 8.07
2.03 ± 5.20
0.18 ± 0.32
1.08 ± 0.25
12.31 ± 7.41
2.34 ± 5.25
0.18 ± 0.31
1.13 ± 0.24
18.61 ± 7.60
1.65 ± 4.83
0.19 ± 0.33
1.09 ± 0.29
11.76 ± 7.03
2.25 ± 4.84
0.20 ± 0.30
1.12 ± 0.20
18.68 ± 7.63
1.74 ± 5.12
0.18 ± 0.33
The correlations between prognostic factors and ADC values or DCE-MRI quantitative parameters
The associations between prognostic factors and ADC values or DCE-MRI quantitative parameters
Comparisons of enhancement quantitative parameters or ADC values with subgroups of prognostic factors
The P value of multiple comparisons of enhancement quantitative parameters or ADC values with subgroups of prognostic factors
Prognostic value of ADC values or DCE-MRI quantitative parameters
Area under curve (AUC) of ROC for ADC values or DCE-MRI quantitative parameters versus prognosis of breast cancer
0.560 to 0.718
0.653 to 0.800
0.435 to 0.600
0.466 to 0.630
Hazard ratio (HR) of ADC values or DCE-MRI quantitative parameters on prognosis of breast cancer
95% CI of HR
0.768 to 36.026
1.030 to 1.134
0.854 to 1.185
0.065 to 11.960
Currently, the correlation between DCE-MRI quantitative parameters and prognosis factors of breast cancer, including enhanced morphology, tumor size, pathological grade, and lymph node status, is still in the preliminary stage, and the results of different studies are quite different [23, 24]. Koo et al. investigated the correlations between parameters (Ktrans, Kep, and Ve) of 70 IDCs and tumor size . Their results revealed that mean values of Ktrans and Kep were higher in tumors with size > 2 cm than that with size ≦ 2 cm, respectively, whereas mean values of Ve were lower in tumors with size > 2 cm than that with size ≦ 2 cm. In consistent with this report, our study revealed that the mean values of Ktrans and Kep were apparently higher in tumors with size ≥ 2 cm than that with size < 2 cm, respectively. Our results also showed that significant differences were observed for the Ktrans values of subgroups of tumor size, but not for Kep and Ve values. However, Spearman correlation test showed a significant and positive correlation between Ktrans or Kep values and tumor size. In addition, DWI technology is the only imaging method to observe the microscopic movement of water molecules in living body [25–27]. It can reflect the spatial composition information of human tissue and the functional changes of water molecules of various tissues in the pathophysiological state [25–28]. We further found that though no significant differences were observed for the correlation between ADC values and tumor size, the ADC values between subgroups of tumor sizes were significantly different. These results suggested that Ktrans had the highest efficiency in evaluation of tumor size in this study. However, several studies reported that DWI shows strong potential as an adjunct MRI technique to reduce breast biopsies , demonstrating better performance than DCE-MRI [29–32]. Boulogianni et al. reported that combination with DCE improves the accuracy of cancer detection .
Histologic grade of tumor is a routine and important task for clinical diagnosis of IDC . Recent research reported a positive correlation between ipsilateral whole-breast vascularity and tumor size, nuclear grade, and histologic grade, which manifested as higher Ktrans and Kep values [34–36]. Kim et al. studied 50 patients with different histologic grades of breast cancer lesions and showed that there was no significant difference in Ktrans values between higher and lower histologic grades . However, our results revealed that only the Ktrans values had significant difference between subgroups of histologic grade. Thus, although there is no completely consistent view on the relationship between these parameters and histologic grade, these researches highly suggested that high histologic grade is clearly associated with higher Ktrans.
The presence of axillary lymph node metastasis is an important prognostic factor in patients with breast cancer, determining the followed management after surgery . Our results also showed that Ktrans has significant positive correlation with LNM, while only Ve values exhibit significant difference between subgroups of LN, which is firstly reported in this study to date. Bahri et al. reported that LN(+) group has higher Kep than the LN(−) group . The inconsistent results may be due to the relatively small sample size.
Breast cancer patients with ER- and PR-positive are sensitive to endocrine therapy, the survival rate is high, and the prognosis is relatively good . When the ER and PR expression was negative, more contrast agent backflows from extravascular and extracellular space back to the tumor capillary cavity, indicating the capillary permeability is higher. Studies have shown that ER can reduce vascular endothelial growth factor (VEGF) levels and inhibit tumor angiogenesis . Thus, compared with ER and PR positive expression, in tumor with ER and PR negative expression, the neovascularization is richer and the hemodynamic parameters may be higher . Our study showed that ER and PR expression has negative correlation with ADC and Ktrans values, respectively. Hence, in consistent with previous researches, our results suggested that ADC and Ktrans values can reflect the information that the contrast agent diffuses from inner vessel into outer vessel. However, Ktrans value is a better indicator for the prediction of ER and PR expression compared to ADC value.
HER2, a product of a proto-oncogene, is a growth factor receptor with tyrosine kinase activity, which is rarely expressed in normal tissues . Whether it is expressed or not is closely related to the occurrence and prognosis of breast cancer . Our results showed that there was statistically negative correlation between HER2 and Kep values and positive correlation between HER2 and ADC values. However, some researches revealed that ADC values of IDC with HER2-positive are lower than those of IDC with HER2-negative because of increased cellularity . These contradictory results may be due to the different values of b used in the determination of ADC . Our results were highly consistent with the reports of Park et al., where b values of 0 and 1000 , the same with this studies, were used in the measurements of ADC values. Thus, we suggest that ADC, followed Kep, is the best predictor of HER2, which is closely related to the occurrence and prognosis of breast cancer.
Ki-67 is a nuclear antigen, which is associated with cell proliferation . The higher the expression level of Ki-67 in tumor, the risk of recurrence is obviously increased . In the current study, there were notably positive correlations between Ki-67 and Ktrans values. Consistent with our results, Kim et al. found that the Ktrans values in breast cancer with Ki-67 overexpression were significantly higher in patients with low expression of Ki-67 . However, unlike Kim et al.’s study, there was no correlation between Kep value and Ki-67 in the present study. Thus, we suggested that the higher the Ktrans value is the tumor differentiation is worse, the degree of malignancy is higher, and possibility of tumor recurrence is greater.
In this study, higher Ktrans values are closely associated with higher rise of poor prognosis of breast cancer, while ADC, Kep, and Ve cannot predict prognosis of breast cancer. A similar result reported that ADC value was a good parameter in prediction of malignant breast tumors; however, ADC value was not a predictor of patient prognosis . In addition, another study showed that compared with traditional DWI, diffusion kurtosis imaging (DKI) can better distinguish between benign and malignant breast lesions. Also, this article showed that Kep performed better than Ktrans . However, our results suggested that Ktrans value is the best one in predicting prognosis of breast cancer. Therefore, further studies needs to be performed.
We found that with higher values of Ktrans, ADC within IDC patients are associated with poor prognostic factors. Higher Kep values in IDC were closely positively correlated with tumor size and negatively correlated with PR and HER2. Ktrans value is helpful in predicting prognosis of breast cancer.
This work was supported by Nanjing Medical Science and Technology Development Project - Digital Mammography and Magnetic Resonance Quantitative Imaging Mode in Subclinical Breast Cancer [Grant Number: YKK14181].
Availability of data and materials
The analyzed data sets generated during the study are available from the corresponding author on reasonable request.
FL and MW conceived and designed the experiments. FL and MW performed the experiments and analyzed the data. HL contributed to the reagents, materials, analysis tools. All authors read and approved the final manuscript.
Ethics approval and consent to participate
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
Consent for publication
The authors declare that they have no competing interests.
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- Akasbi Y, Bennis S, Abbass F, Znati K, Joutei KA, Amarti A, et al. Clinicopathological, therapeutic and prognostic features of the triple-negative tumors in moroccan breast cancer patients (experience of Hassan II university hospital in Fez). BMC Res Notes. 2011;4(1):1–6.View ArticleGoogle Scholar
- Blanchard A, Shiu R, Booth S, Sorensen G, Decorby N, Nistor A, et al. Gene expression profiling of early involuting mammary gland reveals novel genes potentially relevant to human breast cancer. Front Biosci. 2007;12(6):2221–32.PubMedView ArticleGoogle Scholar
- Lindström LS, Karlsson E, Wilking UM, Johansson U, Hartman J, Lidbrink EK, et al. Clinically used breast cancer markers such as estrogen receptor, progesterone receptor, and human epidermal growth factor receptor 2 are unstable throughout tumor progression. J Clin Oncol. 2012;30(21):2601.PubMedView ArticleGoogle Scholar
- Cuzick J, Dowsett M, Pineda S, Wale C, Salter J, Quinn E, et al. Prognostic value of a combined estrogen receptor, progesterone receptor, Ki-67, and human epidermal growth factor receptor 2 immunohistochemical score and comparison with the Genomic Health recurrence score in early breast cancer. J Clin Oncol. 2011;29(32):4273.PubMedView ArticleGoogle Scholar
- Kapoor P, Prasad SVAV, editors. Image processing for early diagnosis of breast cancer using infrared images. The 2nd International Conference on Computer and Automation Engineering (ICCAE). 2010; pp. 564–566.Google Scholar
- Egeland TA, Simonsen TG, Gaustad JV, Gulliksrud K, Ellingsen C, Rofstad EK. Dynamic contrast-enhanced magnetic resonance imaging of tumors: preclinical validation of parametric images. Radiat Res. 2009;172(3):339–47.PubMedView ArticleGoogle Scholar
- Franiel T, Hamm B, Hricak H. Dynamic contrast-enhanced magnetic resonance imaging and pharmacokinetic models in prostate cancer. Eur Radiol. 2011;21(3):616–26.PubMedView ArticleGoogle Scholar
- Donaldson SB, Bonington SC, Kershaw LE, Cowan R, Lyons J, Elliott T, et al. Dynamic contrast-enhanced MRI in patients with muscle-invasive transitional cell carcinoma of the bladder can distinguish between residual tumour and post-chemotherapy effect. Eur J Radiol. 2013;82(12):2161–8.PubMedView ArticleGoogle Scholar
- Montemurro F, Russo F, Martincich L, Cirillo S, Gatti M, Aglietta M, et al. Dynamic contrast enhanced magnetic resonance imaging in monitoring bone metastases in breast cancer patients receiving bisphosphonates and endocrine therapy. Acta Radiol. 2004;45(1):71–4.PubMedView ArticleGoogle Scholar
- Morrow M. Magnetic resonance imaging for screening, diagnosis, and eligibility for breast-conserving surgery: promises and pitfalls. Surg Oncol Clin N Am. 2010;19(3):475–92.PubMedView ArticleGoogle Scholar
- Schnapauff D, Zeile M, Niederhagen MB, Fleige B, Tunn PU, Hamm B, et al. Diffusion-weighted echo-planar magnetic resonance imaging for the assessment of tumor cellularity in patients with soft-tissue sarcomas. J Magn Reson Imaging. 2009;29(6):1355.PubMedView ArticleGoogle Scholar
- Barchetti F, Panebianco V. Multiparametric MRI for recurrent prostate cancer post radical prostatectomy and postradiation therapy. Biomed Res Int. 2014;2014(1):316272.PubMedPubMed CentralGoogle Scholar
- Budiharto T, Joniau S, Lerut E, Van den Bergh L, Mottaghy F, Deroose CM, et al. Prospective evaluation of 11C-choline positron emission tomography/computed tomography and diffusion-weighted magnetic resonance imaging for the nodal staging of prostate cancer with a high risk of lymph node metastases. Eur Urol. 2011;60(1):125–30.PubMedView ArticleGoogle Scholar
- Tatsumi Y, Tanigawa N, Nishimura H, Nomura E, Mabuchi H, Matsuki M, et al. Preoperative diagnosis of lymph node metastases in gastric cancer by magnetic resonance imaging with ferumoxtran-10. Gastric Cancer. 2006;9(2):120–8.PubMedView ArticleGoogle Scholar
- Orguc S, Basara I, Coskun T. Diffusion-weighted MR imaging of the breast: comparison of apparent diffusion coefficient values of normal breast tissue with benign and malignant breast lesions. Singap Med J. 2012;53(11):737–43.Google Scholar
- Razek AA, Gaballa G, Denewer A, Nada N. Invasive ductal carcinoma: correlation of apparent diffusion coefficient value with pathological prognostic factors. NMR Biomed. 2010;23(6):619–23.PubMedView ArticleGoogle Scholar
- Park SH, Choi HY, Hahn SY. Correlations between apparent diffusion coefficient values of invasive ductal carcinoma and pathologic factors on diffusion-weighted MRI at 3.0 Tesla. J Magn Reson Imaging. 2015;41(1):175–82.PubMedView ArticleGoogle Scholar
- Tofts PS, Brix G, Buckley DL, Evelhoch JL, Henderson E, Knopp MV, et al. Estimating kinetic parameters from dynamic contrast-enhanced T(1)-weighted MRI of a diffusable tracer: standardized quantities and symbols. J Magn Reson Imaging. 1999;10(3):223–32.PubMedView ArticleGoogle Scholar
- Turetschek K, Floyd E, Helbich T, Roberts TP, Shames DM, Wendland MF, et al. MRI assessment of microvascular characteristics in experimental breast tumors using a new blood pool contrast agent (MS-325) with correlations to histopathology. J Magn Reson Imaging. 2001;14(3):237.PubMedView ArticleGoogle Scholar
- Abramson RG, Arlinghaus LR, Weis JA, Li X, Dula AN, Chekmenev EY, et al. Current and emerging quantitative magnetic resonance imaging methods for assessing and predicting the response of breast cancer to neoadjuvant therapy. Breast Cancer Targets Ther. 2012;2012(4):139.View ArticleGoogle Scholar
- Zhang L, Tang M, Min Z, Lu J, Lei X, Zhang X. Accuracy of combined dynamic contrast-enhanced magnetic resonance imaging and diffusion-weighted imaging for breast cancer detection: a meta-analysis. Acta radiologica (Stockholm, Sweden : 1987). 2015;57(6):3264.Google Scholar
- Aribal E, Asadov R, Ramazan A, Ugurlu MÜ, Kaya H. Multiparametric breast MRI with 3T: effectivity of combination of contrast enhanced MRI, DWI and 1H single voxel spectroscopy in differentiation of Breast tumors. Eur J Radiol. 2016;85(5):979.PubMedView ArticleGoogle Scholar
- Koo HR, Cho N, Song IC, Kim H, Chang JM, Yi A, et al. Correlation of perfusion parameters on dynamic contrast-enhanced MRI with prognostic factors and subtypes of breast cancers. J Magn Reson Imaging. 2012;36(1):145–51.PubMedView ArticleGoogle Scholar
- Bahri S, Chen JH, Yu HJ, Kuzucan A, Nalcioglu O, Su MY. Can dynamic contrast-enhanced MRI (DCE-MRI) predict tumor recurrence and lymph node status in patients with breast cancer? Ann Oncol. 2008;19(4):822.PubMedPubMed CentralView ArticleGoogle Scholar
- Avcu S, Arslan H, Unal O, Kotan C, Izmirli M. The role of diffusion-weighted MR imaging and ADC values in the diagnosis of gastric tumors. JBR-BTR. 2012;95(1):1–5.Google Scholar
- Pereira FP, Martins G, Carvalhaes dORV. Diffusion magnetic resonance imaging of the breast. Magn Reson Imaging Clin North Am. 2011;19(1):95.View ArticleGoogle Scholar
- Budde MD, Frank JA. Neurite beading is sufficient to decrease the apparent diffusion coefficient after ischemic stroke. Proc Natl Acad Sci. 2010;107(32):14472–7.PubMedView ArticleGoogle Scholar
- Cui XY, Chen HW. Role of diffusion-weighted magnetic resonance imaging in the diagnosis of extrahepatic cholangiocarcinoma. World J Gastroenterol. 2010;16(25):3196.PubMedPubMed CentralView ArticleGoogle Scholar
- Partridge SC, McDonald ES. Diffusion weighted magnetic resonance imaging of the breast: protocol optimization, interpretation, and clinical applications. Magn Reson Imaging Clin N Am. 2013;21(3):601–24.PubMedPubMed CentralView ArticleGoogle Scholar
- Boulogianni G, Chryssogonidis I, Drevelegas A. Diffusion weighted MRI and spectroscopy in invasive carcinoma of the breast at 3Tesla. Correlation with dynamic contrast enhancement and pathologic findings. Hippokratia. 2016;20(3):192–7.PubMedPubMed CentralGoogle Scholar
- Yoshito T, Ayako TT, Keigo E. Magnetic resonance (MR) differential diagnosis of breast tumors using apparent diffusion coefficient (ADC) on 1.5-T. J Magn Reson Imaging. 2010;30(2):249–55.Google Scholar
- Chen X, Li WL, Zhang YL, Wu Q, Guo YM, Bai ZL. Meta-analysis of quantitative diffusion-weighted MR imaging in the differential diagnosis of breast lesions. BMC Cancer. 2010;10(1):693.PubMedPubMed CentralView ArticleGoogle Scholar
- Fidalgo F, Rodrigues TC, Pinilla M, Silva AG, Maciel MS, Rosenberg C, et al. Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast. Tumor Biol. 2015;36(3):1835–48.View ArticleGoogle Scholar
- Li L, Wang K, Sun X, Wang K, Sun Y, Zhang G, et al. Parameters of dynamic contrast-enhanced MRI as imaging markers for angiogenesis and proliferation in human breast cancer. Med Sci Monit. 2015;21(2):376–82.PubMedPubMed CentralGoogle Scholar
- Han M, Kim TH, Kang DK, Kim KS, Yim H. Prognostic role of MRI enhancement features in patients with breast cancer: value of adjacent vessel sign and increased ipsilateral whole-breast vascularity. AJR Am J Roentgenol. 2012;199(4):921.PubMedView ArticleGoogle Scholar
- Ji YK, Kim SH, Yun JK, Kang BJ, An YY, Lee AW, et al. Enhancement parameters on dynamic contrast enhanced breast MRI: do they correlate with prognostic factors and subtypes of breast cancers? Magn Reson Imaging. 2015;33(1):72–80.View ArticleGoogle Scholar
- Sendur MAN, Aksoy S, Ozdemir NY, Yazici O, Zengin N, Altundag K. The efficacy of adjuvant trastuzumab in HER-2 positive breast cancer with axillary lymph node metastases according to the treatment duration. Curr Med Res Opin. 2014;186(12):1342–8.Google Scholar
- Kim TJ, Lee A, Choi YJ, Song BJ, Yim HW, Kang CS. Prognostic significance of high expression of ER-beta in surgically treated ER-positive breast cancer following endocrine therapy. J Breast Cancer. 2012;15(1):79–86.PubMedPubMed CentralView ArticleGoogle Scholar
- Buteau-Lozano H, Velasco G, Cristofari M, Balaguer P, Perrot-Applanat M. Xenoestrogens modulate vascular endothelial growth factor secretion in breast cancer cells through an estrogen receptor-dependent mechanism. J Endocrinol. 2008;196(2):399.PubMedView ArticleGoogle Scholar
- Pelzer T, Jazbutyte V, Hu K, Segerer S, Nahrendorf M, Nordbeck P, et al. The estrogen receptor-alpha agonist 16 alpha-LE2 inhibits cardiac hypertrophy and improves hemodynamic function in estrogen-deficient spontaneously hypertensive rats. Cardiovasc Res. 2005;67(4):604–12.PubMedView ArticleGoogle Scholar
- Gagliato DM, Jardim DL, Marchesi MS, Hortobagyi GN. Mechanisms of resistance and sensitivity to anti-HER2 therapies in HER2+ breast cancer. Oncotarget. 2016;7(39):64431.View ArticleGoogle Scholar
- Howell SJ, Wardley AM, Armstrong AC. Re: Ki67 index, HER2 status, and prognosis of patients with luminal B breast cancer. J Natl Cancer Inst. 2009;101(24):1730–1.PubMedView ArticleGoogle Scholar
- Yoshikawa MI, Ohsumi S, Sugata S, Kataoka M, Takashima S, Mochizuki T, et al. Relation between cancer cellularity and apparent diffusion coefficient values using diffusion-weighted magnetic resonance imaging in breast cancer. Radiat Med. 2008;26(4):222–6.PubMedView ArticleGoogle Scholar
- Halvorsen OJ, Haukaas SA, Akslen LA. Combined loss of PTEN and p27 expression is associated with tumor cell proliferation by Ki-67 and increased risk of recurrent disease in localized prostate cancer. Clin Cancer Res. 2003;9(4):1474–9.PubMedGoogle Scholar
- Kim SH, Cha ES, Kim HS, Kang BJ, Choi JJ, Ji HJ, et al. Diffusion-weighted imaging of breast cancer: correlation of the apparent diffusion coefficient value with prognostic factors. J Magn Reson Imaging. 2010;30(3):615–20.View ArticleGoogle Scholar
- Li TYT, Li L, Lu L, Zhuo Y, Lian J, Xiong Y, Kong D, Li K. Use of diffusion kurtosis imaging and quantitative dynamic contrast-enhanced MRI for the differentiation of breast tumors. J Magn Reson Imaging. 2018;48:1358–66.PubMedView ArticleGoogle Scholar