4.7 Article

First-in-Humans Study of 68Ga-DOTA-Siglec-9, a PET Ligand Targeting Vascular Adhesion Protein 1

Journal

JOURNAL OF NUCLEAR MEDICINE
Volume 62, Issue 4, Pages 577-583

Publisher

SOC NUCLEAR MEDICINE INC
DOI: 10.2967/jnumed.120.250696

Keywords

dosimetry; Ga-68; kinetics; PET; vascular adhesion protein 1; whole-body distribution

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Sialic acid-binding immunoglubulinlike lectin 9 (Siglec-9) is a potential PET tracer for imaging inflammation in healthy males, with favorable biodistribution. The radiopharmaceutical was well tolerated and showed promise in detecting arthritis, comparable to F-18-FDG. Additional studies in rheumatoid arthritis patients are planned to further assess its safety and efficacy.
Sialic acid-binding immunoglubulinlike lectin 9 (Siglec-9) is a ligand of vascular adhesion protein 1. A Ga-68-labeled peptide of Siglec-9, Ga-68-DOTA-Siglec-9, holds promise as a novel PET tracer for imaging of inflammation. This first-in-humans study investigated the safety, tolerability, biodistribution, and radiation dosimetry of this radiopharmaceutical. Methods: Six healthy men underwent dynamic whole-body PET/CT. Serial venous blood samples were drawn from 1 to 240 min after intravenous injection of 162 +/- 4 MBq of Ga-68-DOTA-Siglec-9. In addition to y-counting, the plasma samples were analyzed by high-performance liquid chromatography to detect intact tracer and radioactive metabolites. Radiation doses were calculated using the OLINDA/EXM software, version 2.2. In addition, a patient with early rheumatoid arthritis was studied with both Ga-68-DOTA-Siglec-9 and F-18-FDG PET/CT to determine the ability of the new tracer to detect arthritis. Results: Ga-68-DOTA-Siglec-9 was well tolerated by all subjects. Ga-68-DOTA-Siglec-9 was rapidly cleared from the blood circulation, and several radioactive metabolites were detected. The organs with the highest absorbed doses were the urinary bladder wall (0.38 mSv/MBq) and kidneys (0.054 mSv/MBq). The mean effective dose was 0.022 mSv/MBq (range, 0.020-0.024 mSv/MBq). Most importantly, however, Ga-68-DOTA-Siglec-9 was comparable to F-18-FDG in detecting arthritis. Conclusion: Intravenous injection of Ga-68-DOTA-Siglec-9 was safe and biodistribution was favorable for testing of the tracer in larger group of patients with rheumatoid arthritis, as is planned for the next phase of clinical trials. The effective radiation dose of Ga-68-DOTA-Siglec-9 was within the same range as the effective radiation doses of other Ga-68-labeled tracers. Injection of 150 MBq of Ga-68-DOTA-Siglec-9 would expose a subject to 3.3 mSv. These findings support the possible repeated clinical use of Ga-68-DOTA-Siglec-9, such as in trials to elucidate the treatment efficacy of novel drug candidates.

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