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External radiation exposure, excretion, and effective half-life in Lu-PSMA-targeted therapies.

作者信息

Kurth J, Krause B J, Schwarzenböck S M, Stegger L, Schäfers M, Rahbar K

机构信息

Department of Nuclear Medicine, Rostock University Medical Center, Gertrudenplatz 1, 18057, Rostock, Germany.

Department of Nuclear Medicine, University Hospital Muenster, Muenster, Germany.

出版信息

EJNMMI Res. 2018 Apr 12;8(1):32. doi: 10.1186/s13550-018-0386-4.


DOI:10.1186/s13550-018-0386-4
PMID:29651569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5897276/
Abstract

BACKGROUND: Prostate-specific membrane antigen (PSMA)-targeted therapy with Lu-PSMA-617 is a therapeutic option for patients with metastatic castration-resistant prostate cancer (mCRPC). To optimize the therapy procedure, it is necessary to determine relevant parameters to define radiation protection and safety necessities. Therefore, this study aimed at estimating the ambient radiation exposure received by the patient. Moreover, the excreted activity was quantified. RESULTS: In total, 50 patients with mCRPC and treated with Lu-PSMA-617 (mean administered activity 6.3 ± 0.5 GBq) were retrospectively included in a bi-centric study. Whole-body dose rates were measured at a distance of 2 m at various time points after application of Lu-PSMA-617, and effective half-lives for different time points were calculated and compared. Radiation exposure to the public was approximated using the dose integral. For the estimation of the excreted activity, whole body measurements of 25 patients were performed at 7 time points. Unbound Lu-PSMA-617 was rapidly cleared from the body. After 4 h, approximately 50% and, after 12 h, approximately 70% of the administered activity were excreted, primarily via urine. The mean dose rates were the following: 3.6 ± 0.7 μSv/h at 2 h p. i., 1.6 ± 0.6 μSv/h at 24 h, 1.1 ± 0.5 μSv/h at 48 h, and 0.7 ± 0.4 μSv/h at 72 h. The mean effective half-life of the cohort was 40.5 ± 9.6 h (min 21.7 h; max 85.7 h). The maximum dose to individual members of the public per treatment cycle was ~ 250 ± 55 μSv when the patient was discharged from the clinic after 48 h and ~ 190 ± 36 μSv when the patient was discharged after 72 h. CONCLUSIONS: In terms of the radiation exposure to the public, Lu-PSMA is a safe option of radionuclide therapy. As usually four (sometimes more) cycles of the therapy are performed, it must be conducted in a way that ensures that applicable legal requirements can be followed. In other words, the radiation exposure to the public and the concentration of activity in wastewater must be sub-marginal. Therefore, in certain countries, hospitalization of these patients is mandatory.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/2389cfc2f70b/13550_2018_386_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/86219e2574c3/13550_2018_386_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/11aaad0f41da/13550_2018_386_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/2389cfc2f70b/13550_2018_386_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/86219e2574c3/13550_2018_386_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/11aaad0f41da/13550_2018_386_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2ec/5897276/2389cfc2f70b/13550_2018_386_Fig3_HTML.jpg

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[1]
External radiation exposure, excretion, and effective half-life in Lu-PSMA-targeted therapies.

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[3]
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引用本文的文献

[1]
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Ann Oncol. 2025-7-16

[2]
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Ann Nucl Med. 2025-6-23

[3]
Targeted radioligand therapy: physics and biology, internal dosimetry and other practical aspects during Lu/Ac treatment in neuroendocrine tumors and metastatic prostate cancer.

Theranostics. 2025-3-18

[4]
Radioactivity levels in the saliva of patients undergoing targeted radioligand therapy with [Lu]Lu-PSMA-I&T and [Lu]Lu-DOTA-TOC.

Clin Oral Investig. 2025-4-11

[5]
First-in-Human Phase 0 Study of AB001, a Prostate-Specific Membrane Antigen-Targeted Pb Radioligand, in Patients with Metastatic Castration-Resistant Prostate Cancer.

J Nucl Med. 2025-5-1

[6]
Efficacy of innovative systemic treatments in combination with radiotherapy for bone metastases: a GEMO (the European Study Group of Bone Metastases) state of the art.

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[7]
Radiation Safety Assessment of 177Lu-DOTATATE Intra-arterial Peptide Receptor Therapy (PRRT).

Indian J Nucl Med. 2024

[8]
Development of a homotrimeric PSMA radioligand based on the NOTI chelating platform.

EJNMMI Radiopharm Chem. 2024-12-11

[9]
Radiation safety and dialysate analysis in hemodialysis following Lu-177-PSMA-617 therapy: A case report.

Radiol Case Rep. 2024-11-14

[10]
Radiation exposure and protection advice after [Lu]Lu-DOTA-TATE therapy in China.

EJNMMI Res. 2024-11-28

本文引用的文献

[1]
Variations in the practice of molecular radiotherapy and implementation of dosimetry: results from a European survey.

EJNMMI Phys. 2017-12-4

[2]
PSMA targeted radioligandtherapy in metastatic castration resistant prostate cancer after chemotherapy, abiraterone and/or enzalutamide. A retrospective analysis of overall survival.

Eur J Nucl Med Mol Imaging. 2017-10-12

[3]
Chemokine receptor - Directed imaging and therapy.

Methods. 2017-9-12

[4]
Repeated Lu-Labeled PSMA-617 Radioligand Therapy Using Treatment Activities of Up to 9.3 GBq.

J Nucl Med. 2017-8-10

[5]
Lu-PSMA-617 radioligand therapy and outcome in patients with metastasized castration-resistant prostate cancer.

Eur J Nucl Med Mol Imaging. 2017-9

[6]
Theranostic Prospects of Gastrin-Releasing Peptide Receptor-Radioantagonists in Oncology.

PET Clin. 2017-7

[7]
Overall survival and response pattern of castration-resistant metastatic prostate cancer to multiple cycles of radioligand therapy using [Lu]Lu-PSMA-617.

Eur J Nucl Med Mol Imaging. 2017-5-9

[8]
Safety of multiple repeated cycles of Lu-octreotate in patients with recurrent neuroendocrine tumour.

Eur J Nucl Med Mol Imaging. 2017-7

[9]
Prospects of Targeting the Gastrin Releasing Peptide Receptor and Somatostatin Receptor 2 for Nuclear Imaging and Therapy in Metastatic Breast Cancer.

PLoS One. 2017-1-20

[10]
Phase 3 Trial of Lu-Dotatate for Midgut Neuroendocrine Tumors.

N Engl J Med. 2017-1-12

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