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Preclinical investigations and first-in-human application of (152)Tb-PSMA-617 for PET/CT imaging of prostate cancer
BACKGROUND: For almost a decade, terbium radioisotopes have been explored for their potential theragnostic application in nuclear medicine: (152)Tb and (155)Tb are the radioisotopes identified for PET or SPECT imaging, while (149)Tb and (161)Tb have suitable decay characteristics for α- and combined...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6658632/ https://www.ncbi.nlm.nih.gov/pubmed/31346796 http://dx.doi.org/10.1186/s13550-019-0538-1 |
Sumario: | BACKGROUND: For almost a decade, terbium radioisotopes have been explored for their potential theragnostic application in nuclear medicine: (152)Tb and (155)Tb are the radioisotopes identified for PET or SPECT imaging, while (149)Tb and (161)Tb have suitable decay characteristics for α- and combined β(−)/Auger-e(−)-therapy, respectively. In the present study, the application of (152)Tb, in combination with PSMA-617 for imaging of prostate-specific membrane antigen (PSMA)-positive prostate cancer, was demonstrated in a preclinical setting and in a patient with metastatic castration-resistant prostate cancer (mCRPC). RESULTS: (152)Tb was produced at the ISOLDE facility at CERN/Geneva, Switzerland, by spallation, followed by on-line mass separation. The chemical separation was performed at Paul Scherrer Institute using chromatographic methods, as previously reported. (152)Tb was employed for labeling PSMA-617, and the radioligand was extensively investigated in vitro to demonstrate similar characteristics to its (177)Lu-labeled counterpart. Preclinical PET/CT imaging studies performed with mice enabled visualization of PSMA-positive PC-3 PIP tumors, while uptake in PSMA-negative PC-3 flu tumors were absent. Based on these promising preclinical results, (152)Tb was shipped to Zentralklinik Bad Berka, Germany, where it was used for labeling of PSMA-617, enabling PET imaging of a patient with mCRPC. PET/CT scans were performed over a period of 25 h post injection (p.i.) of the radioligand (140 MBq). The images were of diagnostic quality, particularly those acquired at later time points, and enabled the detection of the same metastatic lesions and of local recurrent tumor as previously detected by (68)Ga-PSMA-11 PET/CT acquired 45 min p.i. CONCLUSIONS: The results of this study demonstrate the successful preparation and preclinical testing of (152)Tb-PSMA-617 and its first application in a patient with mCRPC. This work could pave the way towards clinical application of other Tb radionuclides in the near future, most importantly (161)Tb, which has promising decay characteristics for an effective treatment of mCRPC patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13550-019-0538-1) contains supplementary material, which is available to authorized users. |
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