<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Keam SP</submitter><funding>Peter MacCallum Foundation</funding><funding>Cancer Council Victoria</funding><funding>Victorian Cancer Agency</funding><funding>National Health and Medical Research Council</funding><funding>Prostate Cancer Foundation</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Prostate cancer (PCa) has a profoundly immunosuppressive microenvironment and is commonly immune excluded with few infiltrative lymphocytes and low levels of immune activation. High-dose radiation has been demonstrated to stimulate the immune system in various human solid tumors. We hypothesized that localized radiation therapy, in the form of high dose-rate brachytherapy (HDRBT), would overcome immune suppression in PCa.&lt;h4>Methods&lt;/h4>To investigate whether HDRBT altered prostate immune context, we analyzed preradiation versus postradiation human tissue from a cohort of 24 patients with localized PCa that received HDRBT as primary treatment (RadBank cohort). We performed Nanostring immune gene expression profiling, digital spatial profiling, and high-throughput immune </pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pagination>e000792</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7319782</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>High dose-rate brachytherapy of localized prostate cancer converts tumors from cold to hot.</pubmed_title><pmcid>PMC7319782</pmcid><pubmed_authors>Sandhu S</pubmed_authors><pubmed_authors>Keam SP</pubmed_authors><pubmed_authors>Halse H</pubmed_authors><pubmed_authors>Caramia F</pubmed_authors><pubmed_authors>Nguyen T</pubmed_authors><pubmed_authors>Neeson PJ</pubmed_authors><pubmed_authors>Van Kooten Losio N</pubmed_authors><pubmed_authors>Darcy PK</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Byrne DJ</pubmed_authors><pubmed_authors>Ryland G</pubmed_authors><pubmed_authors>Blombery P</pubmed_authors><pubmed_authors>Haupt Y</pubmed_authors><pubmed_authors>Mitchell C</pubmed_authors><pubmed_authors>Williams SG</pubmed_authors><pubmed_authors>Haupt S</pubmed_authors></additional><is_claimable>false</is_claimable><name>High dose-rate brachytherapy of localized prostate cancer converts tumors from cold to hot.</name><description>&lt;h4>Background&lt;/h4>Prostate cancer (PCa) has a profoundly immunosuppressive microenvironment and is commonly immune excluded with few infiltrative lymphocytes and low levels of immune activation. High-dose radiation has been demonstrated to stimulate the immune system in various human solid tumors. We hypothesized that localized radiation therapy, in the form of high dose-rate brachytherapy (HDRBT), would overcome immune suppression in PCa.&lt;h4>Methods&lt;/h4>To investigate whether HDRBT altered prostate immune context, we analyzed preradiation versus postradiation human tissue from a cohort of 24 patients with localized PCa that received HDRBT as primary treatment (RadBank cohort). We performed Nanostring immune gene expression profiling, digital spatial profiling, and high-throughput immune </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2026-07-15T22:13:48.961Z</modification><creation>2026-07-09T10:19:51.03Z</creation></dates><accession>S-EPMC7319782</accession><cross_references><pubmed>32581061</pubmed><doi>10.1136/jitc-2020-000792</doi></cross_references></HashMap>