4.7 Article

Prospective Comparison of PET Imaging with PSMA-Targeted 18F-DCFPyL Versus Na18F for Bone Lesion Detection in Patients with Metastatic Prostate Cancer

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 61, Issue 2, Pages 183-188

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.119.227793

Keywords

prostate-specific membrane antigen; PSMA; prostate cancer; bone metastases; (FNa)-F-18; PyL; PET/CT

Funding

  1. Prostate Cancer Foundation Young Investigator Award
  2. European Union's Horizon 2020 research and innovation program under Marie Sklodowska-Curie grant [701983]
  3. Progenics Pharmaceuticals
  4. [CA134675]
  5. [CA183031]
  6. [CA184228]
  7. [EB024495]

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Bone metastases in prostate cancer (PCa) have important prognostic significance, and imaging modalities used for PCa staging should have high sensitivity for detecting such lesions. Prostate-specific membrane antigen (PSMA)-targeted PET radiotracers are promising new agents for imaging PCa. We undertook a head-tohead comparison of PSMA-targeted 2-(3-{1-carboxy-5-[(6-F-18-fluoro-pyridine-3-carbonyl)-amino]-pentyl}-ureido)-pentanedioic acid (F-18-DCFPyL) PET to (NaF)-F-18 PET to determine which modality was more sensitive for the detection of lesions suggestive of bone metastases in a group of patients with metastatic PCa. Methods: Patients with progressive, metastatic PCa were prospectively imaged with both F-18-DCFPyL and (NaF)-F-18 PET/CT, with both scans occurring within 24 h of each other. A consensus 2-reader central review was performed to identify all bone lesions suggestive of sites of PCa involvement on both scans, and maximized SUVs corrected for body weight (SUVmax) and lean body mass (SULmax) were recorded. Soft-tissue lesions were also noted on both scans, and SUVmax, SULmax, and PSMA reporting and data system (RADS) version 1.0 scores were recorded. Data from the 2 scans were compared using a generalized estimating equation. Results: In total, 16 patients meeting all inclusion criteria were enrolled in this study, and 15 of the 16 (93.8%) were imaged with both PET radiotracers. In total, 405 bone lesions suggestive of sites of PCa were identified on at least 1 scan. On F-18-DCFPyL PET/CT, 391 (96.5%) were definitively positive, 4 (1.0%) were equivocally positive, and 10 (2.5%) were negative. On (NaF)-F-18 PET/CT, the corresponding values were 388 (95.8%), 4 (1.0%), and 13 (3.2%). Of the definitively negative lesions on F-18-DCFPyL PET, 8 of 10 (80.0%) were sclerotic and 2 of 10 (20.0%) were infiltrative or marrow-based. Additionally, 12 of 13 (92.3%) of the definitively negative lesions on (NaF)-F-18 PET were infiltrative or marrow-based and 1 of 13 (7.7%) was lytic. Also identified were 78 PSMA-RADS-4, 17 PSMA-RADS-5, and 1 PSMA-RADS-3C soft-tissue lesions. Conclusion: PET/CT imaging using F-18-DCFPyL and (NaF)-F-18 PET had nearly identical sensitivities for the detection of bone lesions in patients with metastatic PCa. As would be expected, PSMA-targeted PET provides more information on soft-tissue disease. There may be little additional value to imaging PCa patients with (NaF)-F-18 after a PSMA-targeted PET scan has already been performed.

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