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Characterizing and Mitigating Bladder Radioactivity on 18F-Fluciclovine PET/CT
Petra Lovrec1,2, David M Schuster3, Robert H Wagner1
1Department of Radiology, Loyola University Medical Center, Maywood, Illinois.
Journal of Nuclear Medicine Technology
|October 13, 2019
Summary
Refraining from voiding before 18F-fluciclovine injection significantly reduces bladder radioactivity, improving prostate cancer recurrence imaging. Voiding before injection leads to higher, potentially obscuring, bladder activity.
Area of Science:
- Nuclear Medicine
- Radiopharmaceutical Imaging
- Oncology
Background:
- 18F-fluciclovine PET is utilized for prostate cancer recurrence detection.
- Clinical observations suggest higher-than-expected bladder excretion of 18F-fluciclovine.
- Radiopharmaceutical package insert indicates minimal urinary excretion within the first 4 hours.
Purpose of the Study:
- To quantify early bladder radioactivity after 18F-fluciclovine administration.
- To assess the impact of voiding protocols on bladder radioactivity.
- To determine if withholding voiding before injection mitigates bladder activity.
Main Methods:
- 159 patients undergoing 18F-fluciclovine PET/CT were divided into two groups: voiding before injection (n=36) and not voiding before injection (n=123).
- Standardized Uptake Values (SUVmax, SUVmean) for bladder, aorta, marrow, and liver were measured.
- Bladder radioactivity was categorized based on SUVmean relative to background organs.
Main Results:
- Overall, 22% of patients exhibited moderate and 8.8% intense bladder activity.
- A negative association was observed between bladder volume and SUVmean.
- The non-voiding group showed significantly lower rates of moderate (17.1% vs 38.9%) and intense (4.9% vs 22.2%) bladder activity compared to the voiding group.
Conclusions:
- Withholding voiding prior to 18F-fluciclovine injection effectively reduces urinary bladder radioactivity.
- This modified protocol is recommended to prevent potential masking or mimicry of prostate cancer recurrence.
- Further investigation into the mechanisms of 18F-fluciclovine bladder accumulation is warranted.
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