» Articles » PMID: 30237212

Evaluation of In-DOTA-5D3, a Surrogate SPECT Imaging Agent for Radioimmunotherapy of Prostate-Specific Membrane Antigen

Overview
Journal J Nucl Med
Specialty Nuclear Medicine
Date 2018 Sep 22
PMID 30237212
Citations 13
Authors
Affiliations
Soon will be listed here.
Abstract

5D3 is a new high-affinity murine monoclonal antibody specific for prostate-specific membrane antigen (PSMA). PSMA is a target for the imaging and therapy of prostate cancer. In-labeled antibodies have been used as surrogates for Lu/Y-labeled therapeutics. We characterized In-DOTA-5D3 by SPECT/CT imaging, tissue biodistribution studies, and dosimetry. Radiolabeling, stability, cell uptake, and internalization of In-DOTA-5D3 were performed by established techniques. Biodistribution and SPECT imaging were done on male nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice bearing human PSMA(+) PC3 PIP and PSMA(-) PC3 flu prostate cancer xenografts on the upper right and left flanks, respectively, at 2, 24, 48, 72, and 192 h after injection. Biodistribution was also evaluated in tumor-free, healthy male CD-1 mice. Blocking studies were performed by coinjection of a 10-fold and 50-fold excess of 5D3 followed by biodistribution at 24 h to determine PSMA binding specificity. The absorbed radiation doses were calculated on the basis of murine biodistribution data, which were translated to a human adult man using organ weights as implemented in OLINDA/EXM. In-DOTA-5D3 was synthesized with specific activity of approximately 2.24 ± 0.74 MBq/μg (60.54 ± 20 μCi/μg). Distribution of In-DOTA-5D3 in PSMA(+) PC3 PIP tumor peaked at 24 h after injection and remained high until 72 h. Uptake in normal tissues, including the blood, spleen, liver, heart, and lungs, was highest at 2 h after injection. Coinjection of In-DOTA-5D3 with a 10- and 50-fold excess of nonradiolabeled antibody significantly reduced PSMA(+) PC3 PIP tumor and salivary gland uptake at 24 h but did not reduce uptake in kidneys and lacrimal glands. Significant clearance of In-DOTA-5D3 from all organs occurred at 192 h. The highest radiation dose was received by the liver (0.5 mGy/MBq), followed by the spleen and kidneys. Absorbed radiation doses to the salivary and lacrimal glands and bone marrow were low. In-DOTA-5D3 is a new radiolabeled antibody for imaging and a surrogate for therapy of malignant tissues expressing PSMA.

Citing Articles

Structure-Activity Relationships and Biological Insights into PSMA-617 and Its Derivatives with Modified Lipophilic Linker Regions.

Schafer M, Bauder-Wust U, Roscher M, Motlova L, Kutilova Z, Remde Y ACS Omega. 2025; 10(7):7077-7090.

PMID: 40028088 PMC: 11865982. DOI: 10.1021/acsomega.4c10142.


Advancements in molecular imaging probes for precision diagnosis and treatment of prostate cancer.

Fang J, Alhaskawi A, Dong Y, Cheng C, Xu Z, Tian J J Zhejiang Univ Sci B. 2025; 26(2):124-144.

PMID: 40015933 PMC: 11867783. DOI: 10.1631/jzus.B2300614.


Performance of PSMA-targeted radiotheranostics in an experimental model of renal cell carcinoma.

Singh R, Thotakura A, Alati S, Lisok A, Jiang Z, Merino V Front Oncol. 2024; 14:1432286.

PMID: 39324008 PMC: 11423292. DOI: 10.3389/fonc.2024.1432286.


Targeting Prostate Cancer Using Bispecific T-Cell Engagers against Prostate-Specific Membrane Antigen.

Das G, Ptacek J, Havlinova B, Nedvedova J, Barinka C, Novakova Z ACS Pharmacol Transl Sci. 2023; 6(11):1703-1714.

PMID: 37974624 PMC: 10644396. DOI: 10.1021/acsptsci.3c00159.


Preclinical Evaluation of a New Series of Albumin-Binding Lu-Labeled PSMA-Based Low-Molecular-Weight Radiotherapeutics.

Boinapally S, Alati S, Jiang Z, Yan Y, Lisok A, Singh R Molecules. 2023; 28(16).

PMID: 37630410 PMC: 10459686. DOI: 10.3390/molecules28166158.


References
1.
Bouchelouche K, Choyke P, Capala J . Prostate specific membrane antigen- a target for imaging and therapy with radionuclides. Discov Med. 2010; 9(44):55-61. PMC: 3410553. View

2.
Erbas B, Tuncel M . Renal Function Assessment During Peptide Receptor Radionuclide Therapy. Semin Nucl Med. 2016; 46(5):462-78. DOI: 10.1053/j.semnuclmed.2016.04.006. View

3.
Smith-Jones P, Vallabhajosula S, Navarro V, Bastidas D, Goldsmith S, Bander N . Radiolabeled monoclonal antibodies specific to the extracellular domain of prostate-specific membrane antigen: preclinical studies in nude mice bearing LNCaP human prostate tumor. J Nucl Med. 2003; 44(4):610-7. View

4.
Vallabhajosula S, Goldsmith S, Hamacher K, Kostakoglu L, Konishi S, Milowski M . Prediction of myelotoxicity based on bone marrow radiation-absorbed dose: radioimmunotherapy studies using 90Y- and 177Lu-labeled J591 antibodies specific for prostate-specific membrane antigen. J Nucl Med. 2005; 46(5):850-8. View

5.
Miyahira A, Pienta K, Morris M, Bander N, Baum R, Fendler W . Meeting report from the Prostate Cancer Foundation PSMA-directed radionuclide scientific working group. Prostate. 2018; 78(11):775-789. DOI: 10.1002/pros.23642. View