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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society of Radiology
2022
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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. |
format | Online Article Text |
id | pubmed-9434735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society of Radiology |
record_format | MEDLINE/PubMed |
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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