<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lahusen A</submitter><funding>Institutional funding of the Department of Internal Medicine I</funding><funding>Universitätsklinikum Ulm</funding><funding>Servier Deutschland GmbH</funding><pagination>202</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12281745</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Prognosis in advanced pancreatic ductal adenocarcinoma (aPDAC) is particularly poor, only few patients benefit from treatment, and there are few biomarkers. The PREDICT trial examined whether first-line time-to-treatment failure (TTF1) predicts second-line treatment failure (TTF2) in aPDAC patients but found no association. We hypothesized that the tumor immune microenvironment (TiME) could correlate with the outcome in this trial and assessed whether tissue features were reflected in peripheral blood.&lt;h4>Methods&lt;/h4>PREDICT patients received 5-FU/LV plus nanoliposomal irinotecan as second-line treatment. We stratified patients by shortest vs. longest TTF2 and analyzed 20 treatment-naïve tumor tissues samples via transcriptomics and immunohistochemistry. Peripheral blood</pubmed_abstract><journal>Molecular cancer</journal><pubmed_title>An immune responsive tumor microenvironment imprints into PBMCs and predicts outcome in advanced pancreatic cancer: lessons from the PREDICT trial.</pubmed_title><pmcid>PMC12281745</pmcid><funding_grant_id>PREDICT</funding_grant_id><pubmed_authors>Budczies J</pubmed_authors><pubmed_authors>Eiseler T</pubmed_authors><pubmed_authors>Seufferlein T</pubmed_authors><pubmed_authors>Stenzinger A</pubmed_authors><pubmed_authors>Schwarzer A</pubmed_authors><pubmed_authors>Hofling S</pubmed_authors><pubmed_authors>Karthaus M</pubmed_authors><pubmed_authors>Lahusen A</pubmed_authors><pubmed_authors>Siegler G</pubmed_authors><pubmed_authors>Becher A</pubmed_authors><pubmed_authors>Lutz MP</pubmed_authors><pubmed_authors>Albus S</pubmed_authors><pubmed_authors>Kirchner M</pubmed_authors><pubmed_authors>Cheung PF</pubmed_authors><pubmed_authors>Kluck K</pubmed_authors><pubmed_authors>Ettrich TJ</pubmed_authors><pubmed_authors>Fang R</pubmed_authors><pubmed_authors>Kleger A</pubmed_authors><pubmed_authors>Siveke JT</pubmed_authors><pubmed_authors>Tannapfel A</pubmed_authors></additional><is_claimable>false</is_claimable><name>An immune responsive tumor microenvironment imprints into PBMCs and predicts outcome in advanced pancreatic cancer: lessons from the PREDICT trial.</name><description>&lt;h4>Background&lt;/h4>Prognosis in advanced pancreatic ductal adenocarcinoma (aPDAC) is particularly poor, only few patients benefit from treatment, and there are few biomarkers. The PREDICT trial examined whether first-line time-to-treatment failure (TTF1) predicts second-line treatment failure (TTF2) in aPDAC patients but found no association. We hypothesized that the tumor immune microenvironment (TiME) could correlate with the outcome in this trial and assessed whether tissue features were reflected in peripheral blood.&lt;h4>Methods&lt;/h4>PREDICT patients received 5-FU/LV plus nanoliposomal irinotecan as second-line treatment. We stratified patients by shortest vs. longest TTF2 and analyzed 20 treatment-naïve tumor tissues samples via transcriptomics and immunohistochemistry. Peripheral blood</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-07-15T06:25:39.019Z</modification><creation>2025-08-12T03:05:03.339Z</creation></dates><accession>S-EPMC12281745</accession><cross_references><pubmed>40696453</pubmed><doi>10.1186/s12943-025-02406-7</doi></cross_references></HashMap>