<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(8)</volume><submitter>Lowentritt BH</submitter><funding>Blue Earth Diagnostics</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>&lt;sup>18&lt;/sup>F-Flotufolastat (&lt;sup>18&lt;/sup>F-rhPSMA-7.3) is a newly approved prostate-specific membrane antigen targeting radiopharmaceutical for diagnostic imaging of prostate cancer (PCa). SPOTLIGHT (National Clinical Trials 04186845) evaluated &lt;sup>18&lt;/sup>F-flotufolastat in men with suspected PCa recurrence. Here, we present results of predefined exploratory endpoints from SPOTLIGHT to evaluate the impact of clinical factors on &lt;sup>18&lt;/sup>F-flotufolastat detection rates (DR).&lt;h4>Methods and materials&lt;/h4>The impact of baseline prostate-specific antigen (PSA), PSA doubling time (PSAdt), and International Society of Urologic Pathology Grade Group (GG) on &lt;sup>18&lt;/sup>F-flotufolastat DR was evaluated among all SPOTLIGHT patients with an evaluable scan, with DR stratified</pubmed_abstract><journal>Advances in radiation oncology</journal><pagination>101532</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11298587</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of Clinical Factors on &lt;sup>18&lt;/sup>F-Flotufolastat Detection Rates in Men With Recurrent Prostate Cancer: Exploratory Analysis of the Phase 3 SPOTLIGHT Study.</pubmed_title><pmcid>PMC11298587</pmcid><pubmed_authors>Chapin BF</pubmed_authors><pubmed_authors>Helfand BT</pubmed_authors><pubmed_authors>Chau A</pubmed_authors><pubmed_authors>Uchio EM</pubmed_authors><pubmed_authors>Lowentritt BH</pubmed_authors><pubmed_authors>SPOTLIGHT Study Group</pubmed_authors><pubmed_authors>Michalski JM</pubmed_authors><pubmed_authors>Morris MA</pubmed_authors><pubmed_authors>Schuster DM</pubmed_authors><pubmed_authors>Davis P</pubmed_authors><pubmed_authors>Jani AB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of Clinical Factors on &lt;sup>18&lt;/sup>F-Flotufolastat Detection Rates in Men With Recurrent Prostate Cancer: Exploratory Analysis of the Phase 3 SPOTLIGHT Study.</name><description>&lt;h4>Purpose&lt;/h4>&lt;sup>18&lt;/sup>F-Flotufolastat (&lt;sup>18&lt;/sup>F-rhPSMA-7.3) is a newly approved prostate-specific membrane antigen targeting radiopharmaceutical for diagnostic imaging of prostate cancer (PCa). SPOTLIGHT (National Clinical Trials 04186845) evaluated &lt;sup>18&lt;/sup>F-flotufolastat in men with suspected PCa recurrence. Here, we present results of predefined exploratory endpoints from SPOTLIGHT to evaluate the impact of clinical factors on &lt;sup>18&lt;/sup>F-flotufolastat detection rates (DR).&lt;h4>Methods and materials&lt;/h4>The impact of baseline prostate-specific antigen (PSA), PSA doubling time (PSAdt), and International Society of Urologic Pathology Grade Group (GG) on &lt;sup>18&lt;/sup>F-flotufolastat DR was evaluated among all SPOTLIGHT patients with an evaluable scan, with DR stratified</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2025-04-22T21:49:21.28Z</modification><creation>2024-11-09T01:55:08.406Z</creation></dates><accession>S-EPMC11298587</accession><cross_references><pubmed>39104875</pubmed><doi>10.1016/j.adro.2024.101532</doi></cross_references></HashMap>