<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(52)</volume><submitter>Cha YJ</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Inflammatory myofibroblastic tumors (IMTs) are rare mesenchymal neoplasms that are composed of myofibroblastic cells accompanied by inflammatory infiltrate. We investigated the immune profiles of IMTs, including PD-L1 expression and proportion of CD8+ tumor-infiltrating lymphocytes (TILs), as well as its clinicopathological characteristics according to &lt;i>ALK&lt;/i> gene rearrangementstatus.&lt;h4>Methods&lt;/h4>Twenty-eight IMTs from 25 patients were retrieved from our pathology files (2005-2015), and their clinicopathological parameters and outcomes were analyzed. Immunohistochemistry (IHC) was performed using whole-tissue sections to detect PD-L1 and CD8 expression, and fluorescent in situ hybridization (FISH) analysis and IHC were performed using tissue microarrays to identif</pubmed_abstract><journal>Oncotarget</journal><pagination>89465-89474</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5685684</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>PD-L1 expression and CD8+ tumor-infiltrating lymphocytes are associated with ALK rearrangement and clinicopathological features in inflammatory myofibroblastic tumors.</pubmed_title><pmcid>PMC5685684</pmcid><pubmed_authors>Shim HS</pubmed_authors><pubmed_authors>Cha YJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>PD-L1 expression and CD8+ tumor-infiltrating lymphocytes are associated with ALK rearrangement and clinicopathological features in inflammatory myofibroblastic tumors.</name><description>&lt;h4>Background&lt;/h4>Inflammatory myofibroblastic tumors (IMTs) are rare mesenchymal neoplasms that are composed of myofibroblastic cells accompanied by inflammatory infiltrate. We investigated the immune profiles of IMTs, including PD-L1 expression and proportion of CD8+ tumor-infiltrating lymphocytes (TILs), as well as its clinicopathological characteristics according to &lt;i>ALK&lt;/i> gene rearrangementstatus.&lt;h4>Methods&lt;/h4>Twenty-eight IMTs from 25 patients were retrieved from our pathology files (2005-2015), and their clinicopathological parameters and outcomes were analyzed. Immunohistochemistry (IHC) was performed using whole-tissue sections to detect PD-L1 and CD8 expression, and fluorescent in situ hybridization (FISH) analysis and IHC were performed using tissue microarrays to identif</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Oct</publication><modification>2025-04-22T21:19:22.879Z</modification><creation>2019-03-27T03:01:51Z</creation></dates><accession>S-EPMC5685684</accession><cross_references><pubmed>29163763</pubmed><doi>10.18632/oncotarget.20948</doi></cross_references></HashMap>