Safety, Dosimetry, and Feasibility of [<sup>68</sup>Ga]Ga-PSMA-R2 as an Imaging Agent in Patients with Biochemical Recurrence or Metastatic Prostate Cancer
Prostate-specific membrane antigen (PSMA) is highly expressed in most prostate cancers (PCs). PET and CT imaging studies using <sup>68</sup>Ga-labeled PSMA ligands demonstrated the specific localization of <sup>68</sup>Ga in PC lesions and distant metastatic lesions. [<sup>68</sup>Ga]Ga-PSMA-R2 (<sup>68</sup>Ga-PSMA-R2) is a PSMA-targeted PET/CT radiotracer with potential diagnostic applications. <b>Methods:</b> PROfind (NCT03490032) was a phase 1/2, open-label, multicenter study of administration of 3 MBq/kg of <sup>68</sup>Ga-PSMA-R2 (from >150 to ≤250 MBq) in patients with biochemical recurrence (BCR) or metastatic PC (mPC). Participants underwent baseline conventional imaging (CT/MRI or bone scan) and PET/CT. Whole-body PET/CT imaging sequences were obtained between 20 min and 4 h after injection. Primary endpoints were safety and tolerability; secondary endpoints included biodistribution, potential lesion identification, pharmacokinetics, and dosimetry. Potential lesions were identified by 2 masked expert panels; a third panel evaluated the identified lesions. <b>Results:</b> Six patients with BCR were enrolled into phase 1, and 24 patients with BCR or mPC (<i>n</i> = 12 each) into phase 2. Thirteen treatment-emergent adverse events were reported, including 1 serious adverse event (ileus), unrelated to drug administration. All adverse events were mild or moderate and deemed not related to <sup>68</sup>Ga-PSMA-R2. Peak blood concentration of <sup>68</sup>Ga-PSMA-R2 was typically observed approximately 5 min after injection, steadily decreasing over 6 h. Mean absorbed radiation dose was highest in the urinary bladder wall (0.120 mGy/MBq) and kidney (0.061 mGy/MBq). No other organ mean absorbed radiation dose exceeded 0.020 mGy/MBq. Mean absorbed radiation doses in the salivary and lacrimal glands were 0.016 and 0.008 mGy/MBq, respectively. Mean total body absorbed radiation dose was 0.014 mGy/MBq. Mean effective total body dose was 0.015 mSv/MBq (range, 0.012-0.018 mSv/MBq). <sup>68</sup>Ga-PSMA-R2 PET/CT detected 85 lesions in 22 participants at 1 h after injection and 103 lesions in 22 participants at 2 h after injection. Conventional imaging detected 49 lesions in 8 participants with mPC but none in participants with BCR. <b>Conclusion:</b> <sup>68</sup>Ga-PSMA-R2 was well tolerated, with no drug-related treatment-emergent adverse events. Safety and preliminary imaging performance data support further development of <sup>68</sup>Ga-PSMA-R2 as a diagnostic agent in patients with PC.
Authors
- Lilja B. Sólnes (ORCID: https://orcid.org/0000-0002-2192-7425)
- Darko Pucar (ORCID: https://orcid.org/0000-0001-6597-5149)
- Elena Castaldi
- Beilei He (ORCID: https://orcid.org/0000-0002-4115-0115)
- Daniela Chicco
- Steven P. Rowe (ORCID: https://orcid.org/0000-0003-2897-4694)
- Frank I. Lin (ORCID: https://orcid.org/0000-0003-3539-1454)
- Benedikt Feuerecker
- Thomas A. Hope (ORCID: https://orcid.org/0000-0002-2228-5823)
- Liza Lindenberg (ORCID: https://orcid.org/0000-0002-8514-0648)
- Nancy E. Gilbert
Institutions
- University of North Carolina at Chapel Hill (US)
- Novartis (Switzerland) (CH)
- National Institutes of Health (US)
- Johns Hopkins University (US)
- University of California, San Francisco (US)
- Johns Hopkins Medicine (US)
- Yale University (US)
- Novartis (United States) (US)
- Novartis (Italy) (IT)
- National Cancer Institute (US)
- Technical University of Munich (DE)
Publication Details
- Journal
- Journal of Nuclear Medicine
- Published
- 2025-02-06
- DOI
- https://doi.org/10.2967/jnumed.124.268318
- Citations
- 4
- Primary Topic
- Radiopharmaceutical Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 5.44