Preliminary study for non-invasive measurement of estrogen receptor by [18F]FES-PET/CT
Not Applicable
- Conditions
- Breast cancer
- Registration Number
- JPRN-UMIN000019336
- Lead Sponsor
- Saitama Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1) Patient who is pregnant or who has the possibility of pregnancy 2) Patient who have difficulty in performing PET/CT exam by the severe pain or bad condition 3) Patient who are determined as not appropriate for attending this study by the investigators
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method a) Validity of PET imaging process, b) relationship between the uptake in 18F-FES PET/CT and the pathological expression of estrogen receptor at primary lesion of breast cancer, and c) relationship between the uptake in 18F-FES PET/CT and the results of other imaging modalities, are evaluated by the visual comparison by radiologists and statistical analysis by the results of pathology and other imaging modalities, when 18F-FES PET/CT images of all the cases will be acquired.
- Secondary Outcome Measures
Name Time Method