<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Goff PH</submitter><funding>Sarcoma Foundation of America</funding><funding>ImmunoPrism</funding><funding>NCI NIH HHS</funding><funding>NIH</funding><pagination>1701-1711</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9953754</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(8)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>To characterize changes in the soft-tissue sarcoma (STS) tumor immune microenvironment induced by standard neoadjuvant therapy with the goal of informing neoadjuvant immunotherapy trial design.&lt;h4>Experimental design&lt;/h4>Paired pre- and postneoadjuvant therapy specimens were retrospectively identified for 32 patients with STSs and analyzed by three modalities: multiplexed IHC, NanoString, and RNA sequencing with ImmunoPrism analysis.&lt;h4>Results&lt;/h4>All 32 patients, representing a variety of STS histologic subtypes, received neoadjuvant radiotherapy and 21 (66%) received chemotherapy prior to radiotherapy. The most prevalent immune cells in the tumor before neoadjuvant therapy were myeloid cells (45% of all immune cells) and B cells (37%), with T (13%) and natural killer (NK</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pubmed_title>Neoadjuvant Therapy Induces a Potent Immune Response to Sarcoma, Dominated by Myeloid and B Cells.</pubmed_title><pmcid>PMC9953754</pmcid><funding_grant_id>L30 CA153318</funding_grant_id><funding_grant_id>P30 CA015704</funding_grant_id><funding_grant_id>R01 CA223498</funding_grant_id><funding_grant_id>R01CA244872</funding_grant_id><funding_grant_id>CA180380</funding_grant_id><funding_grant_id>R01 CA244872</funding_grant_id><pubmed_authors>Goff PH</pubmed_authors><pubmed_authors>Jones RL</pubmed_authors><pubmed_authors>LaFranzo NA</pubmed_authors><pubmed_authors>Ricciotti R</pubmed_authors><pubmed_authors>McClanahan TK</pubmed_authors><pubmed_authors>Riolobos L</pubmed_authors><pubmed_authors>Smythe KS</pubmed_authors><pubmed_authors>LaFleur BJ</pubmed_authors><pubmed_authors>Kane GM</pubmed_authors><pubmed_authors>Cranmer LD</pubmed_authors><pubmed_authors>Wagner MJ</pubmed_authors><pubmed_authors>Pierce RH</pubmed_authors><pubmed_authors>Spraker MB</pubmed_authors><pubmed_authors>Pollack SM</pubmed_authors><pubmed_authors>Thompson MJ</pubmed_authors><pubmed_authors>Chen EY</pubmed_authors><pubmed_authors>Loggers ET</pubmed_authors><pubmed_authors>Kim TS</pubmed_authors><pubmed_authors>Blumenschein WM</pubmed_authors><pubmed_authors>Seo YD</pubmed_authors><pubmed_authors>Earls J</pubmed_authors><pubmed_authors>Murphy E</pubmed_authors><pubmed_authors>He Q</pubmed_authors><pubmed_authors>Mantilla JG</pubmed_authors><pubmed_authors>Flanagan KC</pubmed_authors><pubmed_authors>Campbell JS</pubmed_authors><pubmed_authors>Kim EY</pubmed_authors><pubmed_authors>Schaub SK</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Neoadjuvant Therapy Induces a Potent Immune Response to Sarcoma, Dominated by Myeloid and B Cells.</name><description>&lt;h4>Purpose&lt;/h4>To characterize changes in the soft-tissue sarcoma (STS) tumor immune microenvironment induced by standard neoadjuvant therapy with the goal of informing neoadjuvant immunotherapy trial design.&lt;h4>Experimental design&lt;/h4>Paired pre- and postneoadjuvant therapy specimens were retrospectively identified for 32 patients with STSs and analyzed by three modalities: multiplexed IHC, NanoString, and RNA sequencing with ImmunoPrism analysis.&lt;h4>Results&lt;/h4>All 32 patients, representing a variety of STS histologic subtypes, received neoadjuvant radiotherapy and 21 (66%) received chemotherapy prior to radiotherapy. The most prevalent immune cells in the tumor before neoadjuvant therapy were myeloid cells (45% of all immune cells) and B cells (37%), with T (13%) and natural killer (NK</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-05-28T19:01:54.017Z</modification><creation>2025-02-19T00:13:46.53Z</creation></dates><accession>S-EPMC9953754</accession><cross_references><pubmed>35115306</pubmed><doi>10.1158/1078-0432.ccr-21-4239</doi><doi>10.1158/1078-0432.CCR-21-4239</doi></cross_references></HashMap>