<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>49(13)</volume><submitter>Ruigrok EAM</submitter><funding>Advanced Accelerator Applications</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The radiolabeled gastrin-releasing peptide receptor (GRPR)-targeting antagonist NeoB is a promising radioligand for imaging and therapy of GRPR-expressing malignancies. In the current study, we aimed to discover the target organs of toxicity and the radiotoxic effects to these organs, when repeated dosages of [&lt;sup>177&lt;/sup>Lu]Lu-NeoB are administered to healthy female and male mice.&lt;h4>Methods&lt;/h4>Animals received either 3 injections, with a 7-day interval, of vehicle (control group 1), 1200 pmol [&lt;sup>175&lt;/sup>Lu]Lu-NeoB (control group 2) or 40 MBq/400 pmol, 80 MBq/800 pmol, and 120 MBq/1200 pmol [&lt;sup>177&lt;/sup>Lu]Lu-NeoB (treatment groups 1, 2, and 3, respectively). At week 5, 19, and 43 after the first injection acute, early, and late organ toxicity, respectively, was d</pubmed_abstract><journal>European journal of nuclear medicine and molecular imaging</journal><pagination>4440-4451</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9605926</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety of [&lt;sup>177&lt;/sup>Lu]Lu-NeoB treatment: a preclinical study characterizing absorbed dose and acute, early, and late organ toxicity.</pubmed_title><pmcid>PMC9605926</pmcid><pubmed_authors>de Jong M</pubmed_authors><pubmed_authors>Dalm SU</pubmed_authors><pubmed_authors>Konijnenberg MW</pubmed_authors><pubmed_authors>Rolfo K</pubmed_authors><pubmed_authors>Stuurman DC</pubmed_authors><pubmed_authors>de Blois E</pubmed_authors><pubmed_authors>Verhoeven M</pubmed_authors><pubmed_authors>de Ridder CMA</pubmed_authors><pubmed_authors>Bertarione L</pubmed_authors><pubmed_authors>Ruigrok EAM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety of [&lt;sup>177&lt;/sup>Lu]Lu-NeoB treatment: a preclinical study characterizing absorbed dose and acute, early, and late organ toxicity.</name><description>&lt;h4>Purpose&lt;/h4>The radiolabeled gastrin-releasing peptide receptor (GRPR)-targeting antagonist NeoB is a promising radioligand for imaging and therapy of GRPR-expressing malignancies. In the current study, we aimed to discover the target organs of toxicity and the radiotoxic effects to these organs, when repeated dosages of [&lt;sup>177&lt;/sup>Lu]Lu-NeoB are administered to healthy female and male mice.&lt;h4>Methods&lt;/h4>Animals received either 3 injections, with a 7-day interval, of vehicle (control group 1), 1200 pmol [&lt;sup>175&lt;/sup>Lu]Lu-NeoB (control group 2) or 40 MBq/400 pmol, 80 MBq/800 pmol, and 120 MBq/1200 pmol [&lt;sup>177&lt;/sup>Lu]Lu-NeoB (treatment groups 1, 2, and 3, respectively). At week 5, 19, and 43 after the first injection acute, early, and late organ toxicity, respectively, was d</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2025-04-19T18:52:47.37Z</modification><creation>2024-12-04T08:52:39.04Z</creation></dates><accession>S-EPMC9605926</accession><cross_references><pubmed>35951084</pubmed><doi>10.1007/s00259-022-05926-2</doi></cross_references></HashMap>