Breast Cancer
Conditions
Keywords
PEM Uptake Value, PUV, Standardized Uptake Value, SUV, Malignancies of the Breast, [18F]-FDG-PET/CT scanning, Tumor, positron emission tomography/computed tomography, PET/CT scan
Brief summary
The goal of this clinical research study is to learn if using the PEMFlex Solo II, a high-resolution camera for positron emission tomography (PET) scan imaging, on an area of the body that has, or is suspected to have cancer will give researchers the same or better information about the disease compared to the images taken with a routine PET/computed tomography (CT). Researchers will compare the images taken using the PEMFlex Solo II to the images taken during your scheduled routine PET/CT scan, as well as any additional routine CT scan(s), magnetic resonance imaging (MRI) scan(s), and/or ultrasound image(s) you may have had within the last 30 days or may have in the next 30 days.
Detailed description
If you agree to take part in this study, right after your already scheduled routine PET/CT scan is complete, a study staff member will take you to a separate imaging room located in the same clinic area where your routine PET/CT scan was just performed. You will then sit in a chair as a study staff member positions the PEMFlex Solo II on either side of your breast that has, or is suspected to have cancer. To take images using the PEMFlex Solo II, the breast is placed between two flat panels on the scanning machine and compressed (flattened). The position of the breast for this procedure is similar to getting a mammogram, but the PEMFlex Solo II uses about 50% less force to compress the breast(s). The compression will be repeated on the other breast if you are having scans of both breasts performed. It will take about 20 minutes to set up the PEMFlex Solo II and take the PET scan images. Length of Study: After the PET scan images have been taken using the PEMFlex Solo II, your participation in this study will be over. This is an investigational study. The PEMFlex Solo II is commercially available for PET scan imaging of the breast. Up to 24 patients will take part in this study. All will be enrolled at M. D. Anderson.
Interventions
None listed
Sponsors
M.D. Anderson Cancer Center
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. A signed informed consent. 2. Known or suspected malignancy involving the breast as determined by biopsy, physical examination or noninvasive imaging studies including plain films, CT, MR, ultrasound or nuclear medicine imaging. 3. Scheduled for routine clinical imaging at the ACB PET/CT facility. 4. Participant must be at least 18 years of age.
Exclusion criteria
1. Uncontrolled blood glucose levels (\>200 mg/dl). 2. Patient is unable to comprehend the requirements of the study. 3. Patient is unable to undergo scanning of the known or suspected lesion with the high-resolution PEM (PET) scanner (due to body habitus, inability to comply with positioning requirements, etc.).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Correlation between PUV and SUV of breast malignancies in patients undergoing [18F]-FDG-PET/CT scanning | 20 minutes for imaging using PEMFlex Solo II | Formal quantitative assessment of the correlation between PUVmax values and maximum standardized uptake value (SUVmax) values performed by testing whether the Pearson correlation between these values exceeds 0.7. |
Countries
United States
Outcome results
None listed