<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(1)</volume><submitter>Heinhuis KM</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>Multiple immunostimulatory agonist antibodies have been clinically tested in solid tumors to evaluate the role of targeting glucocorticoid-induced tumor necrosis factor (TNF) receptor-related protein in anticancer treatments.&lt;h4>Objective&lt;/h4>To evaluate the safety and activity of the fully human glucocorticoid-induced TNF receptor-related protein agonist IgG1 monoclonal antibody BMS-986156 with or without nivolumab in patients with advanced solid tumors.&lt;h4>Design, setting, and participants&lt;/h4>This global, open-label, phase 1/2a study of BMS-986156 with or without nivolumab enrolled 292 patients 18 years or older with advanced solid tumors and an Eastern Cooperative Oncology Group performance status of 1 or less. Prior checkpoint inhibitor therapy was allowed. Monother</pubmed_abstract><journal>JAMA oncology</journal><pagination>100-107</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6865300</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety, Tolerability, and Potential Clinical Activity of a Glucocorticoid-Induced TNF Receptor-Related Protein Agonist Alone or in Combination With Nivolumab for Patients With Advanced Solid Tumors: A Phase 1/2a Dose-Escalation and Cohort-Expansion Clinical Trial.</pubmed_title><pmcid>PMC6865300</pmcid><pubmed_authors>Gazzah A</pubmed_authors><pubmed_authors>Heinhuis KM</pubmed_authors><pubmed_authors>Paz-Ares L</pubmed_authors><pubmed_authors>Britschgi C</pubmed_authors><pubmed_authors>Romano E</pubmed_authors><pubmed_authors>Joerger M</pubmed_authors><pubmed_authors>Di Nicola M</pubmed_authors><pubmed_authors>Meniawy T</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Patah P</pubmed_authors><pubmed_authors>Delord JP</pubmed_authors><pubmed_authors>Moreno V</pubmed_authors><pubmed_authors>Curigliano G</pubmed_authors><pubmed_authors>Wang R</pubmed_authors><pubmed_authors>Carlino M</pubmed_authors><pubmed_authors>Rottey S</pubmed_authors><pubmed_authors>Schilder RJ</pubmed_authors><pubmed_authors>O'Byrne K</pubmed_authors><pubmed_authors>Siu LL</pubmed_authors><pubmed_authors>Bajaj G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety, Tolerability, and Potential Clinical Activity of a Glucocorticoid-Induced TNF Receptor-Related Protein Agonist Alone or in Combination With Nivolumab for Patients With Advanced Solid Tumors: A Phase 1/2a Dose-Escalation and Cohort-Expansion Clinical Trial.</name><description>&lt;h4>Importance&lt;/h4>Multiple immunostimulatory agonist antibodies have been clinically tested in solid tumors to evaluate the role of targeting glucocorticoid-induced tumor necrosis factor (TNF) receptor-related protein in anticancer treatments.&lt;h4>Objective&lt;/h4>To evaluate the safety and activity of the fully human glucocorticoid-induced TNF receptor-related protein agonist IgG1 monoclonal antibody BMS-986156 with or without nivolumab in patients with advanced solid tumors.&lt;h4>Design, setting, and participants&lt;/h4>This global, open-label, phase 1/2a study of BMS-986156 with or without nivolumab enrolled 292 patients 18 years or older with advanced solid tumors and an Eastern Cooperative Oncology Group performance status of 1 or less. Prior checkpoint inhibitor therapy was allowed. Monother</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jan</publication><modification>2026-04-12T23:52:11.266Z</modification><creation>2021-02-19T10:38:35Z</creation></dates><accession>S-EPMC6865300</accession><cross_references><pubmed>31697308</pubmed><doi>10.1001/jamaoncol.2019.3848</doi></cross_references></HashMap>