Comparison of [18F]DCFPyL and [18F]FAPI-74 PET/CT imaging in metastatic prostate cancer
Abstract Purpose To compare prostate-specific membrane antigen (PSMA) and fibroblast activation-protein inhibitor (FAPI) targeted PET/CT imaging to assess possible theranostic combination strategies of both tracers in metastatic prostate cancer (mPC). Methods This prospective study enrolled patients with mPC who underwent long-axial field-of-view whole-body PET/CT with 18 F-DCFPyL and 18 F-FAPI-74 within two weeks. Fifteen patients had hormone sensitive (mHSPC) and 24 castration-resistant (mCRPC) disease. Scans were reviewed according to predefined criteria, with up to five metastases per anatomical region evaluated. Lesions were categorized in four groups as skeletal, pelvic nodal, extrapelvic nodal, or visceral. SUVmax and volumetric parameters were measured for each lesion and at the patient level. Results A total of 1365 lesions were identified in 39 patients. 18 F-DCFPyL PET/CT detected 1351 lesions (99%). In contrast, 18 F–FAPI-74 identified only 788 (58%) lesions in the PSMA-guided analysis and 523 (38%) lesions in the independent analysis. Median lesion SUVmax was higher for PSMA (24) than for FAPI (5.4) (p < 0.001). Visceral metastases constituted 3% of lesions with both tracers and tended to be more often FAPI-avid (64%) compared to other lesion groups. Only 14 (1%) of lesions were FAPI-positive and PSMA-negative. In whole-tumor burden analysis, median tracer-positive tumor volume on 18 F-DCFPyL PET/CT was 85 mL and on 18 F-FAPI-74 PET/CT only 10 mL (p < 0.001). Conclusion In mPC, PSMA PET/CT remains the preferred molecular imaging method. Our findings suggest only a limited role of FAPI radioligand therapy. FAPI theranostics should focus on patients with visceral metastases and specific histological subtypes beyond acinar adenocarcinoma. Clinical Trial Registration: EudraCT 2022–003788-13. Registered 21 September 2023
Authors
- Olli Eskola (ORCID: https://orcid.org/0000-0002-9874-5662)
- Otto Ettala (ORCID: https://orcid.org/0000-0003-1011-4602)
- Anna K. Kirjavainen (ORCID: https://orcid.org/0000-0003-3981-2973)
- Kalle Mattila (ORCID: https://orcid.org/0000-0002-9688-9187)
- Simona Malaspina (ORCID: https://orcid.org/0000-0002-2701-8978)
- Mikael Anttinen (ORCID: https://orcid.org/0000-0002-9351-7177)
- Mikael Högerman (ORCID: https://orcid.org/0000-0002-4287-9231)
- Samuli Arvola (ORCID: https://orcid.org/0000-0002-9696-0510)
- Sarita Forsbäck (ORCID: https://orcid.org/0000-0002-6286-7895)
- Pekka Taimen (ORCID: https://orcid.org/0000-0001-8849-4604)
- Anniina Hyväkkä (ORCID: https://orcid.org/0000-0002-0732-2788)
- Heikki Minn (ORCID: https://orcid.org/0000-0002-5878-4333)
- Virva Saunavaara (ORCID: https://orcid.org/0000-0001-7858-5924)
- Maria Sundvall (ORCID: https://orcid.org/0000-0002-0494-2965)
- Marko Seppänen (ORCID: https://orcid.org/0000-0003-2106-9528)
- Veera Sivonen
- Kusti Kilpinen
Institutions
- University of Turku (FI)
- Helsinki University Hospital (FI)
- Turku University Hospital (FI)
- Turku PET Centre (FI)
Publication Details
- Journal
- European Journal of Nuclear Medicine and Molecular Imaging
- Published
- 2026-06-26
- DOI
- https://doi.org/10.1007/s00259-026-08028-5
- Primary Topic
- Peptidase Inhibition and Analysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ida Montinin Säätiö
- Turun Yliopisto
- Syöpäsäätiö
- Turun Yliopistollinen Keskussairaala