<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>61(6)</volume><submitter>Violet J</submitter><pubmed_abstract>&lt;sup>177&lt;/sup>Lu-PSMA-617 is a radioligand with high affinity for prostate-specific membrane antigen (PSMA), enabling targeted β-irradiation of prostate cancer. We have previously reported favorable activity with low toxicity in a prospective phase II trial involving 30 men with metastatic castration-resistant prostate cancer. We now report their longer-term outcomes, including a 20-patient extension cohort and outcomes of subsequent systemic treatments after completion of trial therapy. &lt;b>Methods:&lt;/b> Fifty patients with PSMA-avid metastatic castration-resistant prostate cancer who had progressed after standard therapies received up to 4 cycles of &lt;sup>177&lt;/sup>Lu-PSMA every 6 wk. Endpoints included prostate-specific antigen (PSA) response (Prostate Cancer Working Group 2), toxicity (Com</pubmed_abstract><journal>Journal of nuclear medicine : official publication, Society of Nuclear Medicine</journal><pagination>857-865</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7262220</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Long-Term Follow-up and Outcomes of Retreatment in an Expanded 50-Patient Single-Center Phase II Prospective Trial of &lt;sup>177&lt;/sup>Lu-PSMA-617 Theranostics in Metastatic Castration-Resistant Prostate Cancer.</pubmed_title><pmcid>PMC7262220</pmcid><pubmed_authors>Sandhu S</pubmed_authors><pubmed_authors>Kumar AR</pubmed_authors><pubmed_authors>Jackson P</pubmed_authors><pubmed_authors>Eu P</pubmed_authors><pubmed_authors>Hicks RJ</pubmed_authors><pubmed_authors>Tran B</pubmed_authors><pubmed_authors>Scalzo M</pubmed_authors><pubmed_authors>Ferdinandus J</pubmed_authors><pubmed_authors>Hofman MS</pubmed_authors><pubmed_authors>Kong G</pubmed_authors><pubmed_authors>Iravani A</pubmed_authors><pubmed_authors>Pattison DA</pubmed_authors><pubmed_authors>Mooi J</pubmed_authors><pubmed_authors>Violet J</pubmed_authors><pubmed_authors>Kalff V</pubmed_authors><pubmed_authors>Thang SP</pubmed_authors><pubmed_authors>Akhurst T</pubmed_authors><pubmed_authors>Beaulieu A</pubmed_authors><pubmed_authors>Murphy DG</pubmed_authors><pubmed_authors>Guo C</pubmed_authors><pubmed_authors>Williams S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long-Term Follow-up and Outcomes of Retreatment in an Expanded 50-Patient Single-Center Phase II Prospective Trial of &lt;sup>177&lt;/sup>Lu-PSMA-617 Theranostics in Metastatic Castration-Resistant Prostate Cancer.</name><description>&lt;sup>177&lt;/sup>Lu-PSMA-617 is a radioligand with high affinity for prostate-specific membrane antigen (PSMA), enabling targeted β-irradiation of prostate cancer. We have previously reported favorable activity with low toxicity in a prospective phase II trial involving 30 men with metastatic castration-resistant prostate cancer. We now report their longer-term outcomes, including a 20-patient extension cohort and outcomes of subsequent systemic treatments after completion of trial therapy. &lt;b>Methods:&lt;/b> Fifty patients with PSMA-avid metastatic castration-resistant prostate cancer who had progressed after standard therapies received up to 4 cycles of &lt;sup>177&lt;/sup>Lu-PSMA every 6 wk. Endpoints included prostate-specific antigen (PSA) response (Prostate Cancer Working Group 2), toxicity (Com</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2026-04-30T08:19:13.555Z</modification><creation>2021-02-21T01:07:51Z</creation></dates><accession>S-EPMC7262220</accession><cross_references><pubmed>31732676</pubmed><doi>10.2967/jnumed.119.236414</doi></cross_references></HashMap>