<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Yehan Z</submitter><pubmed_abstract>&lt;h4>Objective&lt;/h4>The choice of neoadjuvant therapy for esophageal squamous cell carcinoma (ESCC) is controversial. This study aims to provide a basis for clinical treatment selection by establishing a predictive model for the efficacy of neoadjuvant immunochemotherapy (NICT).&lt;h4>Methods&lt;/h4>A retrospective analysis of 30 patients was conducted, divided into Response and Non-response groups based on whether they achieved major pathological remission (MPR). Differences in genes and immune microenvironment between the two groups were analyzed through next-generation sequencing (NGS) and multiplex immunofluorescence (mIF). Variables most closely related to therapeutic efficacy were selected through LASSO regression and ROC curves to establish a predictive model. An additional 48 patients were</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1312380</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11079241</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>To develop a prognostic model for neoadjuvant immunochemotherapy efficacy in esophageal squamous cell carcinoma by analyzing the immune microenvironment.</pubmed_title><pmcid>PMC11079241</pmcid><pubmed_authors>Jun H</pubmed_authors><pubmed_authors>Jiayu L</pubmed_authors><pubmed_authors>Jiaxin Y</pubmed_authors><pubmed_authors>Yang L</pubmed_authors><pubmed_authors>Juan J</pubmed_authors><pubmed_authors>Yehan Z</pubmed_authors><pubmed_authors>Min S</pubmed_authors><pubmed_authors>Yi W</pubmed_authors><pubmed_authors>Xueyan C</pubmed_authors><pubmed_authors>Hong Y</pubmed_authors><pubmed_authors>Shangzhi H</pubmed_authors><pubmed_authors>Qifeng W</pubmed_authors><pubmed_authors>Zongyao H</pubmed_authors><pubmed_authors>Sheng Q</pubmed_authors><pubmed_authors>Xuefeng L</pubmed_authors><pubmed_authors>Wenwu H</pubmed_authors></additional><is_claimable>false</is_claimable><name>To develop a prognostic model for neoadjuvant immunochemotherapy efficacy in esophageal squamous cell carcinoma by analyzing the immune microenvironment.</name><description>&lt;h4>Objective&lt;/h4>The choice of neoadjuvant therapy for esophageal squamous cell carcinoma (ESCC) is controversial. This study aims to provide a basis for clinical treatment selection by establishing a predictive model for the efficacy of neoadjuvant immunochemotherapy (NICT).&lt;h4>Methods&lt;/h4>A retrospective analysis of 30 patients was conducted, divided into Response and Non-response groups based on whether they achieved major pathological remission (MPR). Differences in genes and immune microenvironment between the two groups were analyzed through next-generation sequencing (NGS) and multiplex immunofluorescence (mIF). Variables most closely related to therapeutic efficacy were selected through LASSO regression and ROC curves to establish a predictive model. An additional 48 patients were</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-06-01T08:06:19.617Z</modification><creation>2026-04-08T10:51:30.259Z</creation></dates><accession>S-EPMC11079241</accession><cross_references><pubmed>38726002</pubmed><doi>10.3389/fimmu.2024.1312380</doi></cross_references></HashMap>