<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>31(9)</volume><submitter>Rodriguez-Moreno JF</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Neoadjuvant treatment of bladder cancer is evolving, with immunotherapy demonstrating promising activity. PARP inhibition combined with immune activation has been proposed as a synergistic strategy. We conducted a comprehensive molecular characterization of tumors treated with this combination in the neoadjuvant setting to provide crucial results for rational development.&lt;h4>Patients and methods&lt;/h4>A phase II clinical trial was designed to evaluate the combination of anti-PDL1 inhibitor durvalumab and PARP inhibitor olaparib, focusing on biomarker dynamics in both pre- and post-treatment settings. A total of 29 patients were enrolled. Genomic and transcriptomic profiling, as well as analyses of immune cell populations, was conducted at baseline and at the time of cystectom</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pagination>1644-1656</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12010967</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Treatment Efficacy and Molecular Dynamics of Neoadjuvant Durvalumab and Olaparib in Resectable Urothelial Bladder Cancer: The NEODURVARIB Trial.</pubmed_title><pmcid>PMC12010967</pmcid><pubmed_authors>Vazquez S</pubmed_authors><pubmed_authors>Beltran L</pubmed_authors><pubmed_authors>Virizuela JA</pubmed_authors><pubmed_authors>Grana-Castro O</pubmed_authors><pubmed_authors>Rodriguez-Antona C</pubmed_authors><pubmed_authors>de Velasco G</pubmed_authors><pubmed_authors>Berraondo P</pubmed_authors><pubmed_authors>Gajate P</pubmed_authors><pubmed_authors>Madurga R</pubmed_authors><pubmed_authors>Rodriguez-Moreno JF</pubmed_authors><pubmed_authors>Collado R</pubmed_authors><pubmed_authors>Garcia-Donas J</pubmed_authors><pubmed_authors>Font A</pubmed_authors><pubmed_authors>Alvarez-Fernandez C</pubmed_authors><pubmed_authors>Sevillano-Fernandez E</pubmed_authors><pubmed_authors>Ruiz-Llorente S</pubmed_authors><pubmed_authors>Fernandez R</pubmed_authors><pubmed_authors>Lainez N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment Efficacy and Molecular Dynamics of Neoadjuvant Durvalumab and Olaparib in Resectable Urothelial Bladder Cancer: The NEODURVARIB Trial.</name><description>&lt;h4>Purpose&lt;/h4>Neoadjuvant treatment of bladder cancer is evolving, with immunotherapy demonstrating promising activity. PARP inhibition combined with immune activation has been proposed as a synergistic strategy. We conducted a comprehensive molecular characterization of tumors treated with this combination in the neoadjuvant setting to provide crucial results for rational development.&lt;h4>Patients and methods&lt;/h4>A phase II clinical trial was designed to evaluate the combination of anti-PDL1 inhibitor durvalumab and PARP inhibitor olaparib, focusing on biomarker dynamics in both pre- and post-treatment settings. A total of 29 patients were enrolled. Genomic and transcriptomic profiling, as well as analyses of immune cell populations, was conducted at baseline and at the time of cystectom</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 May</publication><modification>2026-06-01T14:52:02.476Z</modification><creation>2025-07-06T03:05:34.909Z</creation></dates><accession>S-EPMC12010967</accession><cross_references><pubmed>40298406</pubmed><doi>10.1158/1078-0432.CCR-24-2890</doi></cross_references></HashMap>