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Exploratory FDG PET/CT Imaging in mCRPC Patients Treated with Sipuleucel-T ± IL-7: A Phase II Trial Subanalysis
Sandeep Surendra Panikar1,2, Dhruv Bansal1, John Crandall1
1Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Metabolic imaging with [18F]-FDG PET/CT offers insights into treatment response in metastatic castration-resistant prostate cancer (mCRPC). Exploratory findings suggest potential for monitoring immunotherapy effects in mCRPC patients.
Area of Science:
- Oncology
- Nuclear Medicine
- Immunotherapy
Background:
- Immunotherapy efficacy in metastatic castration-resistant prostate cancer (mCRPC) is limited.
- There is a need for noninvasive tools to monitor treatment-related biological changes in mCRPC.
Purpose of the Study:
- To evaluate exploratory metabolic imaging correlates using [18F]-FDG PET/CT in mCRPC patients undergoing sipuleucel-T (sip-T) immunotherapy.
- To assess tumor metabolic activity and potential immune-related metabolic changes during treatment.
Main Methods:
- A case series of three mCRPC patients from a sip-T clinical trial (CITN) was analyzed.
- Serial [18F]-FDG PET/CT imaging was performed at baseline and post-therapy.
- Imaging parameters included standardized uptake value (SUVmax, SUVmean), metabolic tumor volume (MTV), and total lesion glycolysis (TLG).
Main Results:
- One patient showed progressive disease with increased MTV and TLG despite stable SUVmax.
- Another patient exhibited transient splenic metabolic increases post-sip-T.
- A third patient, treated with sip-T plus IL-7, demonstrated reduced SUVmax, stable disease, and decreased PSA, suggesting treatment response.
Conclusions:
- [18F]-FDG PET/CT imaging provides exploratory insights into metabolic changes in tumors and immune organs in mCRPC patients.
- Metabolic changes may reflect treatment-associated biological effects and potential immunotherapy response.
- Larger studies are needed to validate these preliminary findings in mCRPC.
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