<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>4(9)</volume><submitter>Chen CT</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>In preclinical models, glucocorticoid receptor (GR) signaling drives resistance to taxane chemotherapy in multiple solid tumors via upregulation of antiapoptotic pathways. ORIC-101 is a potent and selective GR antagonist that was investigated in combination with taxane chemotherapy as an anticancer regimen preclinically and in a phase 1 clinical trial.&lt;h4>Patients and methods&lt;/h4>The ability of ORIC-101 to reverse taxane resistance was assessed in cell lines and xenograft models, and a phase 1 study (NCT03928314) was conducted in patients with advanced solid tumors to determine the dose, safety, and antitumor activity of ORIC-101 with nab-paclitaxel.&lt;h4>Results&lt;/h4>ORIC-101 reversed chemoprotection induced by glucocorticoids in vitro and achieved tumor regressions when comb</pubmed_abstract><journal>Cancer research communications</journal><pagination>2415-2426</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11396014</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ORIC-101, a Glucocorticoid Receptor Antagonist, in Combination with Nab-Paclitaxel in Patients with Advanced Solid Tumors.</pubmed_title><pmcid>PMC11396014</pmcid><pubmed_authors>Hamilton E</pubmed_authors><pubmed_authors>Orr DW</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Barkund SR</pubmed_authors><pubmed_authors>Kummar S</pubmed_authors><pubmed_authors>Abdul-Karim RM</pubmed_authors><pubmed_authors>Davis SL</pubmed_authors><pubmed_authors>Khanna V</pubmed_authors><pubmed_authors>Patel MR</pubmed_authors><pubmed_authors>Chen CT</pubmed_authors><pubmed_authors>Ueno NT</pubmed_authors><pubmed_authors>Daemen A</pubmed_authors><pubmed_authors>Zhou H</pubmed_authors><pubmed_authors>Multani PS</pubmed_authors><pubmed_authors>Xu R</pubmed_authors><pubmed_authors>Sommerhalder D</pubmed_authors><pubmed_authors>Sun JD</pubmed_authors><pubmed_authors>Munster PN</pubmed_authors><pubmed_authors>Chow Maneval E</pubmed_authors><pubmed_authors>Jahchan NS</pubmed_authors><pubmed_authors>Junttila MR</pubmed_authors><pubmed_authors>Pankov A</pubmed_authors><pubmed_authors>Florou V</pubmed_authors><pubmed_authors>Duff M</pubmed_authors><pubmed_authors>Spira AI</pubmed_authors><pubmed_authors>Jauhari S</pubmed_authors><pubmed_authors>Jackson EL</pubmed_authors><pubmed_authors>Tolcher AW</pubmed_authors><pubmed_authors>Kong W</pubmed_authors></additional><is_claimable>false</is_claimable><name>ORIC-101, a Glucocorticoid Receptor Antagonist, in Combination with Nab-Paclitaxel in Patients with Advanced Solid Tumors.</name><description>&lt;h4>Purpose&lt;/h4>In preclinical models, glucocorticoid receptor (GR) signaling drives resistance to taxane chemotherapy in multiple solid tumors via upregulation of antiapoptotic pathways. ORIC-101 is a potent and selective GR antagonist that was investigated in combination with taxane chemotherapy as an anticancer regimen preclinically and in a phase 1 clinical trial.&lt;h4>Patients and methods&lt;/h4>The ability of ORIC-101 to reverse taxane resistance was assessed in cell lines and xenograft models, and a phase 1 study (NCT03928314) was conducted in patients with advanced solid tumors to determine the dose, safety, and antitumor activity of ORIC-101 with nab-paclitaxel.&lt;h4>Results&lt;/h4>ORIC-101 reversed chemoprotection induced by glucocorticoids in vitro and achieved tumor regressions when comb</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Sep</publication><modification>2026-06-30T03:16:23.151Z</modification><creation>2025-04-04T11:04:10.124Z</creation></dates><accession>S-EPMC11396014</accession><cross_references><pubmed>39177285</pubmed><doi>10.1158/2767-9764.CRC-24-0115</doi></cross_references></HashMap>