<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rosenblat TL</submitter><funding>NCI NIH HHS</funding><funding>NIH</funding><funding>Lymphoma Foundation, and Actinium Pharmaceuticals, Inc.</funding><pagination>2030-2037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9106874</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(10)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The anti-CD33 antibody lintuzumab has modest activity against acute myeloid leukemia (AML). To increase its potency, lintuzumab was conjugated to actinium-225 (225Ac), a radionuclide yielding 4 α-particles. This first-in-human, phase I trial was conducted to determine the safety, pharmacology, and biological activity of 225Ac-lintuzumab.&lt;h4>Patients and methods&lt;/h4>Eighteen patients (median age, 64 years; range, 45-80) with relapsed or refractory AML received a single infusion of 225Ac-lintuzumab at activities of 18.5 to 148 kBq/kg.&lt;h4>Results&lt;/h4>The maximum tolerated dose was 111 kBq/kg. Dose-limiting toxicities included myelosuppression lasting > 35 days in one patient receiving 148 kBq/kg and death from sepsis in two patients treated with 111 and 148 kBq/kg. Myelosuppre</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Treatment of Patients with Acute Myeloid Leukemia with the Targeted Alpha-Particle Nanogenerator Actinium-225-Lintuzumab.</pubmed_title><pmcid>PMC9106874</pmcid><funding_grant_id>RO1 55349</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><funding_grant_id>P01 CA033049</funding_grant_id><funding_grant_id>R01 CA055349</funding_grant_id><funding_grant_id>PO1 CA33049</funding_grant_id><funding_grant_id>R35 CA241894</funding_grant_id><pubmed_authors>Carrasquillo JA</pubmed_authors><pubmed_authors>Larson SM</pubmed_authors><pubmed_authors>McDevitt MR</pubmed_authors><pubmed_authors>Park JH</pubmed_authors><pubmed_authors>Rosenblat TL</pubmed_authors><pubmed_authors>Scheinberg DA</pubmed_authors><pubmed_authors>Maslak PG</pubmed_authors><pubmed_authors>Pandit-Taskar N</pubmed_authors><pubmed_authors>Douer D</pubmed_authors><pubmed_authors>Cicic D</pubmed_authors><pubmed_authors>Frattini MG</pubmed_authors><pubmed_authors>Jurcic JG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment of Patients with Acute Myeloid Leukemia with the Targeted Alpha-Particle Nanogenerator Actinium-225-Lintuzumab.</name><description>&lt;h4>Purpose&lt;/h4>The anti-CD33 antibody lintuzumab has modest activity against acute myeloid leukemia (AML). To increase its potency, lintuzumab was conjugated to actinium-225 (225Ac), a radionuclide yielding 4 α-particles. This first-in-human, phase I trial was conducted to determine the safety, pharmacology, and biological activity of 225Ac-lintuzumab.&lt;h4>Patients and methods&lt;/h4>Eighteen patients (median age, 64 years; range, 45-80) with relapsed or refractory AML received a single infusion of 225Ac-lintuzumab at activities of 18.5 to 148 kBq/kg.&lt;h4>Results&lt;/h4>The maximum tolerated dose was 111 kBq/kg. Dose-limiting toxicities included myelosuppression lasting > 35 days in one patient receiving 148 kBq/kg and death from sepsis in two patients treated with 111 and 148 kBq/kg. Myelosuppre</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-05-29T16:11:45.459Z</modification><creation>2025-04-04T09:32:15.775Z</creation></dates><accession>S-EPMC9106874</accession><cross_references><pubmed>35247915</pubmed><doi>10.1158/1078-0432.ccr-21-3712</doi><doi>10.1158/1078-0432.CCR-21-3712</doi></cross_references></HashMap>