Development of PSMA-Targeted Alpha Therapy Using [At]PSMA-5.
Astatine (At) is an alpha-emitting nuclide with a 7.2-hour half-life that can be produced using a 30-MeV cyclotron.
APA
Watabe T, Naka S, et al. (2025). Development of PSMA-Targeted Alpha Therapy Using [At]PSMA-5.. Seminars in nuclear medicine. https://doi.org/10.1053/j.semnuclmed.2025.09.005
MLA
Watabe T, et al.. "Development of PSMA-Targeted Alpha Therapy Using [At]PSMA-5.." Seminars in nuclear medicine, 2025.
PMID
41033956
Abstract
Astatine (At) is an alpha-emitting nuclide with a 7.2-hour half-life that can be produced using a 30-MeV cyclotron. In recent years, the number of production sites worldwide has been increasing, attracting growing attention to At. We have developed a novel At-labeled PSMA-targeted agent ([At]PSMA-5). After conducting preclinical evaluations of its antitumor efficacy and safety, we initiated a first-in-human, investigator-initiated clinical trial in patients with metastatic castration-resistant prostate cancer. To date, the drug has been administered to a total of nine patients, and we have reported high accumulation of [At]PSMA-5 in recurrent and metastatic lesions. While further efforts are required for the social implementation of At-based targeted alpha therapy, including the establishment of a supply chain and the accumulation of additional clinical evidence, PSMA-targeted alpha therapy using At represents a promising treatment modality owing to its cyclotron-based production, sustainability, and clean decay characteristics.
같은 제1저자의 인용 많은 논문 (5)
- [Clinical Application of Targeted Alpha Therapy Using Astatine].
- Recent advances in theranostics and oncology PET: emerging radionuclides and targets.
- First-in-human SPECT/CT imaging of [At]PSMA-5: targeted alpha therapy in a patient with refractory prostate cancer.
- First-in-Human Study of [At]NaAt as Targeted α-Therapy in Patients with Radioiodine-Refractory Thyroid Cancer (Alpha-T1 Trial).
- Comparison of the Therapeutic Effects of [At]NaAt and [I]NaI in an NIS-Expressing Thyroid Cancer Mouse Model.