Affiliation:
1. Nuclear Medicine
2. Pathology, Istanbul Training and Research Hospital, University of Health Sciences
3. Clinic of Radiology, Haseki Training and Research Hospital, University of Health Sciences
4. Clinic of Urology, Istanbul Training and Research Hospital, University of Health Sciences, Istanbul, Türkiye.
Abstract
Purpose
Prostate-specific membrane antigen (PSMA)–targeted PET/CT is a well-established imaging method in prostate cancer (PC) for both staging and restaging, and also for theranostic applications. An alternative imaging method is crucial for 15% PSMA-negative cases. We aimed to investigate the contribution of 68Ga-DOTA-FAPI-04 PET/CT to PC imaging.
Patients and Methods
Thirty-six patients diagnosed with PC were included. Patients underwent both 68Ga-PSMA PET/CT and 68Ga-DOTA-FAPI-04 PET/CT imaging within 1 week. In staging group, primary tumor uptake values were compared, and also correlations were done with histopathological findings, MRI findings, and total PSA levels. In biochemical recurrence group, the uptake values in prostatic region and metastases were evaluated to define the local recurrence or metastatic disease.
Results
In staging group, PSMA PET showed increased uptake in the primary lesion area in 14/27 (52%) patients, whereas 20/27 (74%) patients were positive in FAPI-04 PET. FAPI-04 positivity was found to be quite high, such as 54%, in PSMA-negative patients. A significant difference was observed between ISUP grade 1–3 patients and ISUP grade 4–5 patients in FAPI-04 PET (P = 0.03). Local recurrence was detected in 3 patients, pelvic lymph node metastasis in 1 patient, and sacrum metastasis in 1 patient in biochemical recurrence group, and all of the lesions had more intense uptake in PSMA PET than FAPI-04 PET.
Conclusions
FAPI PET imaging seems to have a potential to contribute PSMA PET imaging with FAPI positivity in more than half of PSMA-negative cases. Also, FAPI-targeted radionuclide therapy may be a promising method in patients resistant to PSMA-targeted therapy.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Cited by
2 articles.
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