<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Creasy CA</submitter><funding>NCI</funding><funding>Adelson Medical Research Foundation</funding><funding>National Cancer Institutes</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><pagination>1911-1924</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9064946</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(9)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Adoptive cell therapy (ACT) of tumor-infiltrating lymphocytes (TIL) historically yields a 40%-50% response rate in metastatic melanoma. However, the determinants of outcome are largely unknown.&lt;h4>Experimental design&lt;/h4>We investigated tumor-based genomic correlates of overall survival (OS), progression-free survival (PFS), and response to therapy by interrogating tumor samples initially collected to generate TIL infusion products.&lt;h4>Results&lt;/h4>Whole-exome sequencing (WES) data from 64 samples indicated a positive correlation between neoantigen load and OS, but not PFS or response to therapy. RNA sequencing analysis of 34 samples showed that expression of PDE1C, RTKN2, and NGFR was enriched in responders who had improved PFS and OS. In contrast, the expression of ELFN1 w</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Genomic Correlates of Outcome in Tumor-Infiltrating Lymphocyte Therapy for Metastatic Melanoma.</pubmed_title><pmcid>PMC9064946</pmcid><funding_grant_id>P30CA016672</funding_grant_id><funding_grant_id>P50 CA221703</funding_grant_id><funding_grant_id>#R01CA184845</funding_grant_id><funding_grant_id>P30 CA016672</funding_grant_id><funding_grant_id>R01 CA184845</funding_grant_id><funding_grant_id>#04-7023433</funding_grant_id><funding_grant_id>P50CA221703</funding_grant_id><pubmed_authors>Haymaker C</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Wong MK</pubmed_authors><pubmed_authors>Yee C</pubmed_authors><pubmed_authors>Tomczak K</pubmed_authors><pubmed_authors>Garraway L</pubmed_authors><pubmed_authors>Beroukhim R</pubmed_authors><pubmed_authors>Torres-Cabala CA</pubmed_authors><pubmed_authors>Hoon DSB</pubmed_authors><pubmed_authors>Stewart C</pubmed_authors><pubmed_authors>Diab A</pubmed_authors><pubmed_authors>Creasy CA</pubmed_authors><pubmed_authors>Patel SP</pubmed_authors><pubmed_authors>Amaria RN</pubmed_authors><pubmed_authors>Forget MA</pubmed_authors><pubmed_authors>Karpinets T</pubmed_authors><pubmed_authors>Bernatchez C</pubmed_authors><pubmed_authors>Pilon-Thomas S</pubmed_authors><pubmed_authors>Tawbi H</pubmed_authors><pubmed_authors>Meng YJ</pubmed_authors><pubmed_authors>Sarnaik AA</pubmed_authors><pubmed_authors>Mule JJ</pubmed_authors><pubmed_authors>Hwu P</pubmed_authors><pubmed_authors>Davies MA</pubmed_authors><pubmed_authors>McQuade J</pubmed_authors><pubmed_authors>Glitza IC</pubmed_authors><pubmed_authors>Bustos M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genomic Correlates of Outcome in Tumor-Infiltrating Lymphocyte Therapy for Metastatic Melanoma.</name><description>&lt;h4>Purpose&lt;/h4>Adoptive cell therapy (ACT) of tumor-infiltrating lymphocytes (TIL) historically yields a 40%-50% response rate in metastatic melanoma. However, the determinants of outcome are largely unknown.&lt;h4>Experimental design&lt;/h4>We investigated tumor-based genomic correlates of overall survival (OS), progression-free survival (PFS), and response to therapy by interrogating tumor samples initially collected to generate TIL infusion products.&lt;h4>Results&lt;/h4>Whole-exome sequencing (WES) data from 64 samples indicated a positive correlation between neoantigen load and OS, but not PFS or response to therapy. RNA sequencing analysis of 34 samples showed that expression of PDE1C, RTKN2, and NGFR was enriched in responders who had improved PFS and OS. In contrast, the expression of ELFN1 w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-09T19:29:54.477Z</modification><creation>2025-04-19T22:46:48.897Z</creation></dates><accession>S-EPMC9064946</accession><cross_references><pubmed>35190823</pubmed><doi>10.1158/1078-0432.CCR-21-1060</doi><doi>10.1158/1078-0432.ccr-21-1060</doi></cross_references></HashMap>