<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>21(1)</volume><submitter>Booth SW</submitter><funding>Oxford Experimental Cancer Centre</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>This Phase 2a dose expansion study was performed to assess the safety, tolerability and preliminary efficacy of the maximum tolerated dose of the oral histone de-acetylase (HDAC) inhibitor CXD101 in patients with relapsed / refractory lymphoma or advanced solid organ cancers and to assess HR23B protein expression by immunohistochemistry as a biomarker of HDAC inhibitor sensitivity.&lt;h4>Methods&lt;/h4>Patients with advanced solid-organ cancers with high HR23B expression or lymphomas received CXD101 at the recommended phase 2 dose (RP2D). Key exclusions: corrected QT > 450 ms, neutrophils &lt; 1.5 × 10&lt;sup>9&lt;/sup>/L, platelets &lt; 75 × 10&lt;sup>9&lt;/sup>/L, ECOG > 1. Baseline HR23B expression was assessed by immunohistochemistry.&lt;h4>Results&lt;/h4>Fifty-one patients enrolled between March</pubmed_abstract><journal>BMC cancer</journal><pagination>851</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8306282</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A Phase 2a cohort expansion study to assess the safety, tolerability, and preliminary efficacy of CXD101 in patients with advanced solid-organ cancer expressing HR23B or lymphoma.</pubmed_title><pmcid>PMC8306282</pmcid><pubmed_authors>Rees G</pubmed_authors><pubmed_authors>Kazmi F</pubmed_authors><pubmed_authors>Campo L</pubmed_authors><pubmed_authors>Soilleux E</pubmed_authors><pubmed_authors>Kesavan M</pubmed_authors><pubmed_authors>La Thangue N</pubmed_authors><pubmed_authors>Whittaker J</pubmed_authors><pubmed_authors>Booth SW</pubmed_authors><pubmed_authors>Collins GP</pubmed_authors><pubmed_authors>Royston D</pubmed_authors><pubmed_authors>Hildyard C</pubmed_authors><pubmed_authors>Eyre TA</pubmed_authors><pubmed_authors>Middleton MR</pubmed_authors><pubmed_authors>Kerr D</pubmed_authors><pubmed_authors>Wang LM</pubmed_authors></additional><is_claimable>false</is_claimable><name>A Phase 2a cohort expansion study to assess the safety, tolerability, and preliminary efficacy of CXD101 in patients with advanced solid-organ cancer expressing HR23B or lymphoma.</name><description>&lt;h4>Background&lt;/h4>This Phase 2a dose expansion study was performed to assess the safety, tolerability and preliminary efficacy of the maximum tolerated dose of the oral histone de-acetylase (HDAC) inhibitor CXD101 in patients with relapsed / refractory lymphoma or advanced solid organ cancers and to assess HR23B protein expression by immunohistochemistry as a biomarker of HDAC inhibitor sensitivity.&lt;h4>Methods&lt;/h4>Patients with advanced solid-organ cancers with high HR23B expression or lymphomas received CXD101 at the recommended phase 2 dose (RP2D). Key exclusions: corrected QT > 450 ms, neutrophils &lt; 1.5 × 10&lt;sup>9&lt;/sup>/L, platelets &lt; 75 × 10&lt;sup>9&lt;/sup>/L, ECOG > 1. Baseline HR23B expression was assessed by immunohistochemistry.&lt;h4>Results&lt;/h4>Fifty-one patients enrolled between March</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jul</publication><modification>2026-05-07T23:54:55.056Z</modification><creation>2022-02-11T00:20:49.253Z</creation></dates><accession>S-EPMC8306282</accession><cross_references><pubmed>34301221</pubmed><doi>10.1186/s12885-021-08595-w</doi></cross_references></HashMap>