<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Massi D</submitter><funding>Associazione Italiana per la Ricerca sul Cancro</funding><funding>Fondazione Cariplo</funding><funding>Roche S.P.A.</funding><funding>Azienda Socio Sanitaria Papa Giovanni XXIII, Bergamo, Italy</funding><pagination>308</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6858711</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Clinical response to MAPK inhibitors in metastatic melanoma patients is heterogeneous for reasons still needing to be elucidated. As the patient immune activity contributes to treatment clinical benefit, the pre-existing level of immunity at tumor site may provide biomarkers of disease outcome to therapy. Here we investigated whether assessing the density and spatial tissue distribution of key immune cells in the tumor microenvironment could identify patients predisposed to respond to MAPK inhibitors.&lt;h4>Methods&lt;/h4>Pretreatment tumor biopsies from a total of 213 patients (158 for the training set and 55 for the validation set) treated with BRAF or BRAF/MEK inhibitors within the Italian Melanoma Intergroup were stained with selected immune markers (CD8, CD163, β-catenin,</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>The density and spatial tissue distribution of CD8&lt;sup>+&lt;/sup> and CD163&lt;sup>+&lt;/sup> immune cells predict response and outcome in melanoma patients receiving MAPK inhibitors.</pubmed_title><pmcid>PMC6858711</pmcid><funding_grant_id>12162</funding_grant_id><funding_grant_id>2015-0911</funding_grant_id><pubmed_authors>Rulli E</pubmed_authors><pubmed_authors>Cattaneo L</pubmed_authors><pubmed_authors>Di Guardo L</pubmed_authors><pubmed_authors>Queirolo P</pubmed_authors><pubmed_authors>Galli F</pubmed_authors><pubmed_authors>De Penni R</pubmed_authors><pubmed_authors>Nassini R</pubmed_authors><pubmed_authors>Palmieri G</pubmed_authors><pubmed_authors>Cossa M</pubmed_authors><pubmed_authors>Vallacchi V</pubmed_authors><pubmed_authors>Simi S</pubmed_authors><pubmed_authors>Mandala M</pubmed_authors><pubmed_authors>Baroni G</pubmed_authors><pubmed_authors>Portelli F</pubmed_authors><pubmed_authors>De Logu F</pubmed_authors><pubmed_authors>Tucci M</pubmed_authors><pubmed_authors>Italian Melanoma Intergroup</pubmed_authors><pubmed_authors>Consoli F</pubmed_authors><pubmed_authors>Rivoltini L</pubmed_authors><pubmed_authors>Quaglino P</pubmed_authors><pubmed_authors>Sileni VC</pubmed_authors><pubmed_authors>Massi D</pubmed_authors><pubmed_authors>Valeri B</pubmed_authors><pubmed_authors>Merelli B</pubmed_authors><pubmed_authors>Del Vecchio M</pubmed_authors><pubmed_authors>Guida M</pubmed_authors><pubmed_authors>Di Giacomo AM</pubmed_authors><pubmed_authors>Rodolfo M</pubmed_authors><pubmed_authors>Occelli M</pubmed_authors><pubmed_authors>Carnevale-Schianca F</pubmed_authors><pubmed_authors>Minisini A</pubmed_authors></additional><is_claimable>false</is_claimable><name>The density and spatial tissue distribution of CD8&lt;sup>+&lt;/sup> and CD163&lt;sup>+&lt;/sup> immune cells predict response and outcome in melanoma patients receiving MAPK inhibitors.</name><description>&lt;h4>Background&lt;/h4>Clinical response to MAPK inhibitors in metastatic melanoma patients is heterogeneous for reasons still needing to be elucidated. As the patient immune activity contributes to treatment clinical benefit, the pre-existing level of immunity at tumor site may provide biomarkers of disease outcome to therapy. Here we investigated whether assessing the density and spatial tissue distribution of key immune cells in the tumor microenvironment could identify patients predisposed to respond to MAPK inhibitors.&lt;h4>Methods&lt;/h4>Pretreatment tumor biopsies from a total of 213 patients (158 for the training set and 55 for the validation set) treated with BRAF or BRAF/MEK inhibitors within the Italian Melanoma Intergroup were stained with selected immune markers (CD8, CD163, β-catenin,</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2026-05-01T15:45:17.799Z</modification><creation>2026-04-07T17:04:49.847Z</creation></dates><accession>S-EPMC6858711</accession><cross_references><pubmed>31730502</pubmed><doi>10.1186/s40425-019-0797-4</doi></cross_references></HashMap>