Breast cancer (BC) is the most common cancer diagnosis among women and the incidence is increasing. Prognosis and treatment are dependent on the expression of estrogen receptors (ER) in the tumor. ER status is determined by immunohistochemistry (IHC) on biopsy tissue. The ER expression can change over time and be heterogeneous. The IHC score on ER expression is subjective and can lead to intra and inter observer variability. A new computer image analysis software that can give the exact percentage of colored tumor cells on sectional tumor cuts has been developed. It is also possible to quantify the ER expression non invasive by using the tracer 16α-18F-flour-17β-estradiol (FES) and in vivo positron emission tomography (PET) scans. FES-PET/CT has a high background activity in the liver which complicates the visualization of liver metastases. Theoretically, a new whole body parametric scan method makes it possible to distinguish background activity from uptake in liver metastases. Malignant tumors often have an increased perfusion, and previous studies have found that tumors with low metabolism relative to blood flow have the longest disease free survival (DFS). To the best of our knowledge, no previous studies have examined the correlation between ER expression and blood flow.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
8
16α-18F-fluor-17β-estradiol PET/CT scan
Department of Nuclear Medicine & PET Centre, Aarhus University Hospital
Aarhus N, Denmark
Sensitivity of parametric FES-PET/CT
Examine the sensitivity of parametric FES-PET/CT compared to conventional FES-PET/CT to detect estrogen receptor (ER) positive liver metastases
Time frame: 1 year
Correlation of ER expression
Correlate the ER expression in metastases measured by parametric FES-PET/CT to Visiopharm H-score on biopsy material examined by immunohistochemistry (IHC)
Time frame: 1 year
Examination of the heterogeneity of ER expression in liver metastases
Examine intra-individual heterogeneity of ER expression in liver metastases by FES-PET/CT
Time frame: 1 year
Examination of the heterogeneity of ER expression i metastases
Examine intra-individual heterogeneity of ER expression in metastases in different tissues by FES-PET/CT
Time frame: 1 year
Examination of the heterogeneity of ER expression
Examine the heterogeneity of the ER expression between primary tumor and metastases by FES-PET/CT
Time frame: 1 year
Correlation of tumor blood flow to ER+ cells
Correlate tumor blood flow measured by H215O-PET/CT to the percentage of ER+ cells, measured by both FES-PET/CT and Visiopharm technology
Time frame: 1 year
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