<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(5)</volume><submitter>Huang RSP</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Several studies have shown clinical outcomes data that support the use of &lt;i>CD274 (PD-L1&lt;/i>) copy-number (CN) gains and/or losses as a biomarker for immune checkpoint inhibitor (ICPI). Here, we present the landscape of &lt;i>CD274&lt;/i> CN changes across a large cohort of solid tumor cases and correlate these with PD-L1 protein expression by immunohistochemistry.&lt;h4>Methods&lt;/h4>We analyzed all cases that underwent comprehensive genomic profiling (CGP) testing at Foundation Medicine between August 2014 and June 2020. &lt;i>CD274&lt;/i> CN changes were correlated with PD-L1 expression in tumor types where there were Food and Drug Administration approved companion diagnostic (CDx) claims and the CDx assay was used to assess PD-L1 expression.&lt;h4>Results&lt;/h4>In all, 244 584 samples </pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pagination>e002680</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8112409</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pan-cancer landscape of &lt;i>CD274&lt;/i> (PD-L1) copy number changes in 244 584 patient samples and the correlation with PD-L1 protein expression.</pubmed_title><pmcid>PMC8112409</pmcid><pubmed_authors>Decker B</pubmed_authors><pubmed_authors>Albacker LA</pubmed_authors><pubmed_authors>Murugesan K</pubmed_authors><pubmed_authors>Hiemenz MC</pubmed_authors><pubmed_authors>Huang RSP</pubmed_authors><pubmed_authors>Mata DA</pubmed_authors><pubmed_authors>Pavlick DC</pubmed_authors><pubmed_authors>Ross JS</pubmed_authors><pubmed_authors>Montesion M</pubmed_authors><pubmed_authors>Frampton G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pan-cancer landscape of &lt;i>CD274&lt;/i> (PD-L1) copy number changes in 244 584 patient samples and the correlation with PD-L1 protein expression.</name><description>&lt;h4>Introduction&lt;/h4>Several studies have shown clinical outcomes data that support the use of &lt;i>CD274 (PD-L1&lt;/i>) copy-number (CN) gains and/or losses as a biomarker for immune checkpoint inhibitor (ICPI). Here, we present the landscape of &lt;i>CD274&lt;/i> CN changes across a large cohort of solid tumor cases and correlate these with PD-L1 protein expression by immunohistochemistry.&lt;h4>Methods&lt;/h4>We analyzed all cases that underwent comprehensive genomic profiling (CGP) testing at Foundation Medicine between August 2014 and June 2020. &lt;i>CD274&lt;/i> CN changes were correlated with PD-L1 expression in tumor types where there were Food and Drug Administration approved companion diagnostic (CDx) claims and the CDx assay was used to assess PD-L1 expression.&lt;h4>Results&lt;/h4>In all, 244 584 samples </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-07-16T09:57:41.471Z</modification><creation>2026-07-09T10:49:40.001Z</creation></dates><accession>S-EPMC8112409</accession><cross_references><pubmed>33972391</pubmed><doi>10.1136/jitc-2021-002680</doi></cross_references></HashMap>