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.

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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
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article

Safety, Dosimetry, and Feasibility of [68Ga]Ga-PSMA-R2 as an Imaging Agent in Patients with Biochemical Recurrence or Metastatic Prostate Cancer

Lilja B. Sólnes, Darko Pucar, Elena Castaldi, Beilei He et al.
4 citations
Journal of Nuclear Medicine
Radiopharmaceutical Chemistry and Applications
5.44
article

Safety, Dosimetry, and Feasibility of [68Ga]Ga-PSMA-R2 as an Imaging Agent in Patients with Biochemical Recurrence or Metastatic Prostate Cancer

Lilja B. Sólnes, Darko Pucar, Elena Castaldi, Beilei He, Daniela Chicco, Steven P. Rowe, Frank I. Lin, Benedikt Feuerecker, Thomas A. Hope, Liza Lindenberg, Nancy E. Gilbert
article en
4 citations

Abstract

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.

Journal of Nuclear MedicineVol. 66(3)
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)
Good health and well-being
Openalex Percentile: Top 5%
Radiopharmaceutical Chemistry and Applications
5.44
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