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Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer

OBJECTIVE: (68)Ga-NGUL is a novel prostate-specific membrane antigen (PSMA)-targeting tracer based on Glu-Urea-Lys derivatives conjugated to a 1,4,7-triazacyclononane-N, N′, N″-triacetic acid (NOTA) chelator via a thiourea-type short linker. This phase I clinical trial of (68)Ga-NGUL was conducted t...

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Autores principales: Suh, Minseok, Ryoo, Hyun Gee, Kang, Keon Wook, Jeong, Jae Min, Jeong, Chang Wook, Kwak, Cheol, Cheon, Gi Jeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Radiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434735/
https://www.ncbi.nlm.nih.gov/pubmed/35762185
http://dx.doi.org/10.3348/kjr.2022.0176
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author Suh, Minseok
Ryoo, Hyun Gee
Kang, Keon Wook
Jeong, Jae Min
Jeong, Chang Wook
Kwak, Cheol
Cheon, Gi Jeong
author_facet Suh, Minseok
Ryoo, Hyun Gee
Kang, Keon Wook
Jeong, Jae Min
Jeong, Chang Wook
Kwak, Cheol
Cheon, Gi Jeong
author_sort Suh, Minseok
collection PubMed
description OBJECTIVE: (68)Ga-NGUL is a novel prostate-specific membrane antigen (PSMA)-targeting tracer based on Glu-Urea-Lys derivatives conjugated to a 1,4,7-triazacyclononane-N, N′, N″-triacetic acid (NOTA) chelator via a thiourea-type short linker. This phase I clinical trial of (68)Ga-NGUL was conducted to evaluate the safety and radiation dosimetry of (68)Ga-NGUL in healthy volunteers and the lesion detection rate of (68)Ga-NGUL in patients with prostate cancer. MATERIALS AND METHODS: We designed a prospective, open-label, single-arm clinical trial with two cohorts comprising six healthy adult men and six patients with metastatic prostate cancer. Safety and blood test-based toxicities were monitored throughout the study. PET/CT scans were acquired at multiple time points after administering (68)Ga-NGUL (2 MBq/kg; 96–165 MBq). In healthy adults, absorbed organ doses and effective doses were calculated using the OLINDA/EXM software. In patients with prostate cancer, the rates of detecting suspicious lesions by (68)Ga-NGUL PET/CT and conventional imaging (CT and bone scintigraphy) during the screening period, within one month after recruitment, were compared. RESULTS: All 12 participants (six healthy adults aged 31–32 years and six prostate cancer patients aged 57–81 years) completed the clinical trial. No drug-related adverse events were observed. In the healthy adult group, (68)Ga-NGUL was rapidly distributed, with the highest uptake in the kidneys. The median effective dose coefficient was calculated as 0.025 mSv/MBq, and cumulative activity in the bladder had the highest contribution. In patients with metastatic prostate cancer, 229 suspicious lesions were detected using either (68)Ga-NGUL PET/CT or conventional imaging. Among them, (68)Ga-NGUL PET/CT detected 199 (86.9%) lesions and CT or bone scintigraphy detected 114 (49.8%) lesions. CONCLUSION: (68)Ga-NGUL can be safely applied clinically and has shown a higher detection rate for the localization of metastatic lesions in prostate cancer than conventional imaging. Therefore, (68)Ga-NGUL is a valuable option for prostate cancer imaging.
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spelling pubmed-94347352022-09-07 Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer Suh, Minseok Ryoo, Hyun Gee Kang, Keon Wook Jeong, Jae Min Jeong, Chang Wook Kwak, Cheol Cheon, Gi Jeong Korean J Radiol Nuclear Medicine OBJECTIVE: (68)Ga-NGUL is a novel prostate-specific membrane antigen (PSMA)-targeting tracer based on Glu-Urea-Lys derivatives conjugated to a 1,4,7-triazacyclononane-N, N′, N″-triacetic acid (NOTA) chelator via a thiourea-type short linker. This phase I clinical trial of (68)Ga-NGUL was conducted to evaluate the safety and radiation dosimetry of (68)Ga-NGUL in healthy volunteers and the lesion detection rate of (68)Ga-NGUL in patients with prostate cancer. MATERIALS AND METHODS: We designed a prospective, open-label, single-arm clinical trial with two cohorts comprising six healthy adult men and six patients with metastatic prostate cancer. Safety and blood test-based toxicities were monitored throughout the study. PET/CT scans were acquired at multiple time points after administering (68)Ga-NGUL (2 MBq/kg; 96–165 MBq). In healthy adults, absorbed organ doses and effective doses were calculated using the OLINDA/EXM software. In patients with prostate cancer, the rates of detecting suspicious lesions by (68)Ga-NGUL PET/CT and conventional imaging (CT and bone scintigraphy) during the screening period, within one month after recruitment, were compared. RESULTS: All 12 participants (six healthy adults aged 31–32 years and six prostate cancer patients aged 57–81 years) completed the clinical trial. No drug-related adverse events were observed. In the healthy adult group, (68)Ga-NGUL was rapidly distributed, with the highest uptake in the kidneys. The median effective dose coefficient was calculated as 0.025 mSv/MBq, and cumulative activity in the bladder had the highest contribution. In patients with metastatic prostate cancer, 229 suspicious lesions were detected using either (68)Ga-NGUL PET/CT or conventional imaging. Among them, (68)Ga-NGUL PET/CT detected 199 (86.9%) lesions and CT or bone scintigraphy detected 114 (49.8%) lesions. CONCLUSION: (68)Ga-NGUL can be safely applied clinically and has shown a higher detection rate for the localization of metastatic lesions in prostate cancer than conventional imaging. Therefore, (68)Ga-NGUL is a valuable option for prostate cancer imaging. The Korean Society of Radiology 2022-09 2022-06-20 /pmc/articles/PMC9434735/ /pubmed/35762185 http://dx.doi.org/10.3348/kjr.2022.0176 Text en Copyright © 2022 The Korean Society of Radiology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Nuclear Medicine
Suh, Minseok
Ryoo, Hyun Gee
Kang, Keon Wook
Jeong, Jae Min
Jeong, Chang Wook
Kwak, Cheol
Cheon, Gi Jeong
Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title_full Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title_fullStr Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title_full_unstemmed Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title_short Phase I Clinical Trial of Prostate-Specific Membrane Antigen-Targeting (68)Ga-NGUL PET/CT in Healthy Volunteers and Patients with Prostate Cancer
title_sort phase i clinical trial of prostate-specific membrane antigen-targeting (68)ga-ngul pet/ct in healthy volunteers and patients with prostate cancer
topic Nuclear Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9434735/
https://www.ncbi.nlm.nih.gov/pubmed/35762185
http://dx.doi.org/10.3348/kjr.2022.0176
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