<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Ma J</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>We aimed to report our clinical experience with the use of &lt;sup>225&lt;/sup>Ac-PSMA-617 in the treatment of mCRPC patients.&lt;h4>Methods&lt;/h4>A retrospective analysis was conducted on 29 metastatic castration-resistant prostate cancer (mCRPC) patients treated with &lt;sup>225&lt;/sup>Ac-PSMA-617. Patients underwent treatment at 8-week intervals and discontinued treatment upon disease progression or the occurrence of intolerable adverse effects. We acquired &lt;sup>68&lt;/sup>Ga-PSMA-11 PET/CT images and laboratory test outcomes of patients at baseline and 8 weeks following each treatment. Short-term efficacy was evaluated through the biochemical response of serum prostate-specific antigen (PSA) and molecular tumor response criteria. A follow-up was conducted to assess the long-term effect</pubmed_abstract><journal>Frontiers in oncology</journal><pagination>1516860</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11906306</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The efficacy and safety of &amp;lt;sup&amp;gt;225&amp;lt;/sup&amp;gt;Ac-PSMA-617 in metastatic castration-resistant prostate cancer.</pubmed_title><pmcid>PMC11906306</pmcid><pubmed_authors>Yangqing J</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Ma J</pubmed_authors><pubmed_authors>Zhang C</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Liu G</pubmed_authors></additional><is_claimable>false</is_claimable><name>The efficacy and safety of &amp;lt;sup&amp;gt;225&amp;lt;/sup&amp;gt;Ac-PSMA-617 in metastatic castration-resistant prostate cancer.</name><description>&lt;h4>Background&lt;/h4>We aimed to report our clinical experience with the use of &lt;sup>225&lt;/sup>Ac-PSMA-617 in the treatment of mCRPC patients.&lt;h4>Methods&lt;/h4>A retrospective analysis was conducted on 29 metastatic castration-resistant prostate cancer (mCRPC) patients treated with &lt;sup>225&lt;/sup>Ac-PSMA-617. Patients underwent treatment at 8-week intervals and discontinued treatment upon disease progression or the occurrence of intolerable adverse effects. We acquired &lt;sup>68&lt;/sup>Ga-PSMA-11 PET/CT images and laboratory test outcomes of patients at baseline and 8 weeks following each treatment. Short-term efficacy was evaluated through the biochemical response of serum prostate-specific antigen (PSA) and molecular tumor response criteria. A follow-up was conducted to assess the long-term effect</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-04-04T14:48:08.716Z</modification><creation>2025-04-04T14:48:08.716Z</creation></dates><accession>S-EPMC11906306</accession><cross_references><pubmed>40094004</pubmed><doi>10.3389/fonc.2025.1516860</doi></cross_references></HashMap>