<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Antonarakis ES</submitter><funding>NCI NIH HHS</funding><pagination>4662-4671</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6481607</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(19)</volume><pubmed_abstract>&lt;b>Purpose:&lt;/b> Sipuleucel-T is FDA approved for the treatment of metastatic castration-resistant prostate cancer (mCRPC) based on the IMPACT trial showing a 4.1-month benefit in median overall survival (OS) for patients receiving sipuleucel-T versus control. Although efficacy of sipuleucel-T is well established, its mechanism remains incompletely understood.&lt;b>Patients and Methods:&lt;/b> Patient samples from three sipuleucel-T trials were assessed for peripheral cellular immune responses to the immunogen PA2024 and the target antigen prostatic acid phosphatase (PAP). PAP- and PA2024-specific proliferative and cytolytic responses were characterized to delineate sipuleucel-T-induced immune responses. To quantify potential cytotoxic T lymphocyte (CTL) activity, cell-surface CD107a expression o</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Antigen-Specific CD8 Lytic Phenotype Induced by Sipuleucel-T in Hormone-Sensitive or Castration-Resistant Prostate Cancer and Association with Overall Survival.</pubmed_title><pmcid>PMC6481607</pmcid><funding_grant_id>P30 CA006973</funding_grant_id><pubmed_authors>Petrylak DP</pubmed_authors><pubmed_authors>Quinn DI</pubmed_authors><pubmed_authors>Kibel AS</pubmed_authors><pubmed_authors>Campogan D</pubmed_authors><pubmed_authors>Dearstyne E</pubmed_authors><pubmed_authors>Small EJ</pubmed_authors><pubmed_authors>Harmon M</pubmed_authors><pubmed_authors>Haynes H</pubmed_authors><pubmed_authors>Chang NN</pubmed_authors><pubmed_authors>Antonarakis ES</pubmed_authors><pubmed_authors>Drake CG</pubmed_authors><pubmed_authors>Vu T</pubmed_authors><pubmed_authors>Sheikh NA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antigen-Specific CD8 Lytic Phenotype Induced by Sipuleucel-T in Hormone-Sensitive or Castration-Resistant Prostate Cancer and Association with Overall Survival.</name><description>&lt;b>Purpose:&lt;/b> Sipuleucel-T is FDA approved for the treatment of metastatic castration-resistant prostate cancer (mCRPC) based on the IMPACT trial showing a 4.1-month benefit in median overall survival (OS) for patients receiving sipuleucel-T versus control. Although efficacy of sipuleucel-T is well established, its mechanism remains incompletely understood.&lt;b>Patients and Methods:&lt;/b> Patient samples from three sipuleucel-T trials were assessed for peripheral cellular immune responses to the immunogen PA2024 and the target antigen prostatic acid phosphatase (PAP). PAP- and PA2024-specific proliferative and cytolytic responses were characterized to delineate sipuleucel-T-induced immune responses. To quantify potential cytotoxic T lymphocyte (CTL) activity, cell-surface CD107a expression o</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Oct</publication><modification>2026-05-03T19:31:38.798Z</modification><creation>2019-06-06T22:48:46Z</creation></dates><accession>S-EPMC6481607</accession><cross_references><pubmed>29858218</pubmed><doi>10.1158/1078-0432.ccr-18-0638</doi><doi>10.1158/1078-0432.CCR-18-0638</doi></cross_references></HashMap>