<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Yi JZ</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Immune checkpoint inhibitors (ICIs) have been increasingly used in hepatocellular carcinoma (HCC). Despite emerging evidence indicating that concomitant medications might impact clinical outcomes, their association with ICI efficacy is undefined in HCC.&lt;h4>Methods&lt;/h4>The multicenter cohort included 851 HCC patients receiving ICIs between January 2018 and December 2022 in 13 institutions. Concomitant medications given within 30 days before or after the initiation of ICIs were evaluated in association with survival, tumor response, and treatment-related adverse event (TRAE) occurrence. Concomitant medications administered within 30 days before or after the initiation of ICI therapy were identified and used to categorize patients into user and non-user groups for each me</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>1680015</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12698624</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Concomitant medication use and clinical outcome in hepatocellular carcinoma treated with immune-based therapy: a multicenter analysis.</pubmed_title><pmcid>PMC12698624</pmcid><pubmed_authors>Song HJ</pubmed_authors><pubmed_authors>Wu XT</pubmed_authors><pubmed_authors>Tan GJ</pubmed_authors><pubmed_authors>Chen MS</pubmed_authors><pubmed_authors>Zhou Q</pubmed_authors><pubmed_authors>Zhu ZJ</pubmed_authors><pubmed_authors>Zeng JZ</pubmed_authors><pubmed_authors>Huang CM</pubmed_authors><pubmed_authors>Li L</pubmed_authors><pubmed_authors>Ding K</pubmed_authors><pubmed_authors>Xu J</pubmed_authors><pubmed_authors>Ning SF</pubmed_authors><pubmed_authors>Song YJ</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Zhang JZ</pubmed_authors><pubmed_authors>Lyu N</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Yi JZ</pubmed_authors><pubmed_authors>Yuan DZ</pubmed_authors><pubmed_authors>Guo RP</pubmed_authors><pubmed_authors>Fan YW</pubmed_authors><pubmed_authors>Zhang YN</pubmed_authors><pubmed_authors>You YF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Concomitant medication use and clinical outcome in hepatocellular carcinoma treated with immune-based therapy: a multicenter analysis.</name><description>&lt;h4>Introduction&lt;/h4>Immune checkpoint inhibitors (ICIs) have been increasingly used in hepatocellular carcinoma (HCC). Despite emerging evidence indicating that concomitant medications might impact clinical outcomes, their association with ICI efficacy is undefined in HCC.&lt;h4>Methods&lt;/h4>The multicenter cohort included 851 HCC patients receiving ICIs between January 2018 and December 2022 in 13 institutions. Concomitant medications given within 30 days before or after the initiation of ICIs were evaluated in association with survival, tumor response, and treatment-related adverse event (TRAE) occurrence. Concomitant medications administered within 30 days before or after the initiation of ICI therapy were identified and used to categorize patients into user and non-user groups for each me</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2026-06-06T02:54:43.725Z</modification><creation>2026-05-24T03:12:58.622Z</creation></dates><accession>S-EPMC12698624</accession><cross_references><pubmed>41394828</pubmed><doi>10.3389/fimmu.2025.1680015</doi></cross_references></HashMap>