An -Acetylgalactosamino Dendron-Clearing Agent for High-Therapeutic-Index DOTA-Hapten Pretargeted Radioimmunotherapy.

TitleAn -Acetylgalactosamino Dendron-Clearing Agent for High-Therapeutic-Index DOTA-Hapten Pretargeted Radioimmunotherapy.
Publication TypeJournal Article
Year of Publication2020
AuthorsCheal SM, Patel M, Yang G, Veach D, Xu H, Guo H-F, Zanzonico PB, Axworthy DB, Cheung N-KV, Ouerfelli O, Larson SM
JournalBioconjug Chem
Volume31
Issue3
Pagination501-506
Date Published2020 03 18
ISSN1520-4812
KeywordsAcetylgalactosamine, Animals, Biotin, Cell Line, Tumor, Colorectal Neoplasms, Dendrimers, Haptens, Heterocyclic Compounds, 1-Ring, Humans, Immunoconjugates, Mice, Radioimmunotherapy, Tissue Distribution, Xenograft Model Antitumor Assays
Abstract

Clearing agents (CAs) can rapidly remove nonlocalized targeting biomolecules from circulation for hepatic catabolism, thereby enhancing the therapeutic index (TI), especially for blood (marrow), of the subsequently administered radioisotope in any multistep pretargeting strategy. Herein we describe the synthesis and in vivo evaluation of a fully synthetic glycodendrimer-based CA for DOTA-based pretargeted radioimmunotherapy (DOTA-PRIT). The novel dendron-CA consists of a nonradioactive yttrium-DOTA-Bn molecule attached via a linker to a glycodendron displaying 16 terminal α-thio--acetylgalactosamine (α-SGalNAc) units (CCA α-16-DOTA-Y; molecular weight: 9059 Da). Pretargeting [Lu]LuDOTA-Bn with CCA α-16-DOTA-Y to GPA33-expressing SW1222 human colorectal xenografts was highly effective, leading to absorbed doses of [Lu]LuDOTA-Bn for blood, tumor, liver, spleen, and kidneys of 11.7, 468, 9.97, 5.49, and 13.3 cGy/MBq, respectively. Tumor-to-normal tissues absorbed-dose ratios (i.e., TIs) ranged from 40 (e.g., for blood and kidney) to about 550 for stomach.

DOI10.1021/acs.bioconjchem.9b00736
Alternate JournalBioconjug Chem
PubMed ID31891487
PubMed Central IDPMC7212493
Grant ListP50 CA086438 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R50 CA243895 / CA / NCI NIH HHS / United States
R01 CA233896 / CA / NCI NIH HHS / United States
P01 CA129243 / CA / NCI NIH HHS / United States
Related Institute: 
Molecular Imaging Innovations Institute (MI3)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065