<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(1)</volume><submitter>Jiao X</submitter><pubmed_abstract>The association between genetic variations and immunotherapy benefit has been widely recognized, while such evidence in gastrointestinal cancer remains limited. We analyzed the genomic profile of 227 immunotherapeutic gastrointestinal cancer patients treated with immunotherapy, from the Memorial Sloan Kettering (MSK) Cancer Center cohort. A gastrointestinal immune prognostic signature (GIPS) was constructed using LASSO Cox regression. Based on this signature, patients were classified into two subgroups with distinctive prognoses (p &lt; 0.001). The prognostic value of the GIPS was consistently validated in the Janjigian and Pender cohort (N = 54) and Peking University Cancer Hospital cohort (N = 92). Multivariate analysis revealed that the GIPS was an independent prognostic biomarker. Notably</pubmed_abstract><journal>NPJ precision oncology</journal><pagination>36</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8096820</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer.</pubmed_title><pmcid>PMC8096820</pmcid><pubmed_authors>Shen L</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Lu Z</pubmed_authors><pubmed_authors>Wei X</pubmed_authors><pubmed_authors>Chen H</pubmed_authors><pubmed_authors>Peng Z</pubmed_authors><pubmed_authors>Zhuo N</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Zhang X</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Gong J</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Qi C</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Jiao X</pubmed_authors></additional><is_claimable>false</is_claimable><name>A genomic mutation signature predicts the clinical outcomes of immunotherapy and characterizes immunophenotypes in gastrointestinal cancer.</name><description>The association between genetic variations and immunotherapy benefit has been widely recognized, while such evidence in gastrointestinal cancer remains limited. We analyzed the genomic profile of 227 immunotherapeutic gastrointestinal cancer patients treated with immunotherapy, from the Memorial Sloan Kettering (MSK) Cancer Center cohort. A gastrointestinal immune prognostic signature (GIPS) was constructed using LASSO Cox regression. Based on this signature, patients were classified into two subgroups with distinctive prognoses (p &lt; 0.001). The prognostic value of the GIPS was consistently validated in the Janjigian and Pender cohort (N = 54) and Peking University Cancer Hospital cohort (N = 92). Multivariate analysis revealed that the GIPS was an independent prognostic biomarker. Notably</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2026-05-08T14:54:59.775Z</modification><creation>2022-02-10T09:32:32.957Z</creation></dates><accession>S-EPMC8096820</accession><cross_references><pubmed>33947957</pubmed><doi>10.1038/s41698-021-00172-5</doi></cross_references></HashMap>