<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Jiang Y</submitter><funding>Postdoctoral Science Foundation of Jiangsu Province</funding><funding>16th batch 'Summit of the Six Top Talents' Program of Jiangsu Province</funding><funding>Jiangsu Provincial Health Committee Medical projects</funding><funding>National Natural Science Foundation of China</funding><funding>China Postdoctoral Science Foundation 12th batch Special fund</funding><funding>16th batch ‘Summit of the Six Top Talents’ Program of Jiangsu Province</funding><funding>Natural Science Foundation of Jiangsu Province</funding><pagination>241</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11448477</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>73(12)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Small cell lung cancer (SCLC) is a highly aggressive neuroendocrine tumor with high mortality, and only a limited subset of extensive-stage SCLC (ES-SCLC) patients demonstrate prolonged survival under chemoimmunotherapy, which warrants the exploration of reliable biomarkers. Herein, we built a machine learning-based model using pathomics features extracted from hematoxylin and eosin (H&amp;E)-stained images to classify prognosis and explore its potential association with genomics and TIME.&lt;h4&gt;Methods&lt;/h4>We retrospectively recruited ES-SCLC patients receiving first-line chemoimmunotherapy at Nanjing Jinling Hospital between April 2020 and August 2023. Digital H&amp;E-stained whole-slide images were acquired, and targeted next-generation sequencing, programmed death ligand-1 stai</pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>A random survival forest-based pathomics signature classifies immunotherapy prognosis and profiles TIME and genomics in ES-SCLC patients.</pubmed_title><pmcid>PMC11448477</pmcid><funding_grant_id>45786</funding_grant_id><funding_grant_id>82100095</funding_grant_id><funding_grant_id>WSN-154</funding_grant_id><funding_grant_id>M2022110</funding_grant_id><funding_grant_id>2018K049A</funding_grant_id><funding_grant_id>BK20180139</funding_grant_id><pubmed_authors>Zhang F</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Wu Q</pubmed_authors><pubmed_authors>Zuo X</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Zhan P</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Cheng Q</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Lv T</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Song Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>A random survival forest-based pathomics signature classifies immunotherapy prognosis and profiles TIME and genomics in ES-SCLC patients.</name><description>&lt;h4>Background&lt;/h4>Small cell lung cancer (SCLC) is a highly aggressive neuroendocrine tumor with high mortality, and only a limited subset of extensive-stage SCLC (ES-SCLC) patients demonstrate prolonged survival under chemoimmunotherapy, which warrants the exploration of reliable biomarkers. Herein, we built a machine learning-based model using pathomics features extracted from hematoxylin and eosin (H&amp;E)-stained images to classify prognosis and explore its potential association with genomics and TIME.&lt;h4&gt;Methods&lt;/h4>We retrospectively recruited ES-SCLC patients receiving first-line chemoimmunotherapy at Nanjing Jinling Hospital between April 2020 and August 2023. Digital H&amp;E-stained whole-slide images were acquired, and targeted next-generation sequencing, programmed death ligand-1 stai</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-16T23:55:44.904Z</modification><creation>2026-07-13T03:06:40.949Z</creation></dates><accession>S-EPMC11448477</accession><cross_references><pubmed>39358575</pubmed><doi>10.1007/s00262-024-03829-9</doi></cross_references></HashMap>