<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>23(Suppl 6)</volume><submitter>Lukas R</submitter><pubmed_abstract>Abstract &lt;h4>BACKGROUND&lt;/h4> IDHwt glioblastoma with unmethylated MGMT gene promoter carries a poor prognosis. Preclinical studies have shown that combination of radiotherapy and dual immunotherapy with nivolumab and IDO inhibition significantly prolongs survival of mice with an orthotopic glioblastoma [Ladomersky, et al. CCR 2018;24(11):2559-2573]. In a clinical trial in patients with newly diagnosed glioblastoma with unmethylated MGMT we substituted temozolomide for dual immunotherapy combination. &lt;h4>METHODS&lt;/h4> Phase 1 trial [NCT04047706] using a 3 + 3 dose-escalation design. All received standard radiotherapy (30 x 2 Gy) with addition of once daily oral BMS-986205 and intravenous nivolumab (240mg every 2 weeks) begining on day 1 of radiotherapy and continuing until disease progressio</pubmed_abstract><journal>Neuro-oncology</journal><pagination>vi51-vi52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8598682</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>CTIM-12. A PHASE 1 TRIAL OF IMMUNORADIOTHERAPY WITH THE IDO ENZYME INHIBITOR (BMS-986205) AND NIVOLUMAB IN PATIENTS WITH NEWLY DIAGNOSED MGMT PROMOTER UNMETHYLATED IDHwt GLIOBLASTOMA</pubmed_title><pmcid>PMC8598682</pmcid><pubmed_authors>Gondi V</pubmed_authors><pubmed_authors>Kumthekar P</pubmed_authors><pubmed_authors>Wainwright D</pubmed_authors><pubmed_authors>Lesniak M</pubmed_authors><pubmed_authors>Lukas R</pubmed_authors><pubmed_authors>Sachdev S</pubmed_authors><pubmed_authors>Dixit K</pubmed_authors><pubmed_authors>James D</pubmed_authors><pubmed_authors>Stupp R</pubmed_authors><pubmed_authors>Grimm S</pubmed_authors><pubmed_authors>Lezon R</pubmed_authors><pubmed_authors>Sharp L</pubmed_authors></additional><is_claimable>false</is_claimable><name>CTIM-12. A PHASE 1 TRIAL OF IMMUNORADIOTHERAPY WITH THE IDO ENZYME INHIBITOR (BMS-986205) AND NIVOLUMAB IN PATIENTS WITH NEWLY DIAGNOSED MGMT PROMOTER UNMETHYLATED IDHwt GLIOBLASTOMA</name><description>Abstract &lt;h4>BACKGROUND&lt;/h4> IDHwt glioblastoma with unmethylated MGMT gene promoter carries a poor prognosis. Preclinical studies have shown that combination of radiotherapy and dual immunotherapy with nivolumab and IDO inhibition significantly prolongs survival of mice with an orthotopic glioblastoma [Ladomersky, et al. CCR 2018;24(11):2559-2573]. In a clinical trial in patients with newly diagnosed glioblastoma with unmethylated MGMT we substituted temozolomide for dual immunotherapy combination. &lt;h4>METHODS&lt;/h4> Phase 1 trial [NCT04047706] using a 3 + 3 dose-escalation design. All received standard radiotherapy (30 x 2 Gy) with addition of once daily oral BMS-986205 and intravenous nivolumab (240mg every 2 weeks) begining on day 1 of radiotherapy and continuing until disease progressio</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2025-05-29T16:11:27.524Z</modification><creation>2025-04-06T01:50:30.446Z</creation></dates><accession>S-EPMC8598682</accession><cross_references/></HashMap>