<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Molina-Alejandre M</submitter><funding>Asociación Española Contra el Cáncer</funding><funding>ThermoFisher</funding><funding>Ministry of Science and Innovation</funding><funding>Instituto de Salud Carlos III</funding><funding>FEDER</funding><funding>Comunidad de Madrid</funding><funding>BMS</funding><funding>Andalusian Government</funding><funding>European Union’s Horizon 2020 research and innovation programme</funding><funding>European Regional Development Fund</funding><pagination>e009762</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11492944</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(10)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Loss of human leukocyte antigen (HLA) class I expression and loss of heterozygosity (LOH) are common events implicated in the primary resistance of non-small cell lung cancer (NSCLC) to immunotherapy. However, there is no data on perioperative chemoimmunotherapy (ChIO) efficacy or response mechanisms in the context of HLA class I defects.&lt;h4>Methods&lt;/h4>Baseline HLA class I tumor status (HLA-deficient (HLA-DEF) or HLA-proficient (HLA-PRO)) was determined by DNA LOH combined with immunohistochemistry for protein levels in tissue of 24 patients with NSCLC treated with perioperative nivolumab plus chemotherapy from NADIM trial (NCT03081689). We integrated HLA tumor status with molecular data (programmed death-ligand 1 (PD-L1), TMB, TCR repertoire, TILs populations, bulk RNA</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>Perioperative chemoimmunotherapy induces strong immune responses and long-term survival in patients with HLA class I-deficient non-small cell lung cancer.</pubmed_title><pmcid>PMC11492944</pmcid><funding_grant_id>PIPF-2022/SAL-GL-25283</funding_grant_id><funding_grant_id>TCR sequencing</funding_grant_id><funding_grant_id>PI22/01223</funding_grant_id><funding_grant_id>Ayuda Predoctoral Madrid 2023</funding_grant_id><funding_grant_id>Group CTS-143</funding_grant_id><funding_grant_id>PI23/01054</funding_grant_id><funding_grant_id>CLARIFY 875160</funding_grant_id><funding_grant_id>PI19/01652</funding_grant_id><funding_grant_id>B-CTS-410-UGR-20</funding_grant_id><funding_grant_id>NADIM Clinical Trial</funding_grant_id><funding_grant_id>RTC2017-6502-1 &amp;apos;INmunoSIGHT&amp;apos;</funding_grant_id><funding_grant_id>CP23/00044</funding_grant_id><funding_grant_id>PID2020-115087GB-100</funding_grant_id><funding_grant_id>CPP2022-009545 &amp;apos;STRAGEN-IO&amp;apos;</funding_grant_id><funding_grant_id>RTC2019-007359-1 &amp;apos;BLI-O&amp;apos;</funding_grant_id><pubmed_authors>Massuti B</pubmed_authors><pubmed_authors>Molina-Alejandre M</pubmed_authors><pubmed_authors>Aptsiauri N</pubmed_authors><pubmed_authors>Parra ER</pubmed_authors><pubmed_authors>Martin-Lopez J</pubmed_authors><pubmed_authors>Provencio M</pubmed_authors><pubmed_authors>Casarrubios M</pubmed_authors><pubmed_authors>Casal-Rubio J</pubmed_authors><pubmed_authors>de Castro J</pubmed_authors><pubmed_authors>Martinez JM</pubmed_authors><pubmed_authors>Cobo M</pubmed_authors><pubmed_authors>Nadal E</pubmed_authors><pubmed_authors>Barneto Aranda I</pubmed_authors><pubmed_authors>Sierra-Rodero B</pubmed_authors><pubmed_authors>Munoz-Viana R</pubmed_authors><pubmed_authors>Insa A</pubmed_authors><pubmed_authors>Martinez-Marti A</pubmed_authors><pubmed_authors>Viteri S</pubmed_authors><pubmed_authors>Wistuba II</pubmed_authors><pubmed_authors>Rodriguez-Abreu D</pubmed_authors><pubmed_authors>Calvo V</pubmed_authors><pubmed_authors>Ruiz-Cabello F</pubmed_authors><pubmed_authors>Garrido F</pubmed_authors><pubmed_authors>Megias D</pubmed_authors><pubmed_authors>Martinez-Toledo C</pubmed_authors><pubmed_authors>Perea F</pubmed_authors><pubmed_authors>Cruz-Bermudez A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Perioperative chemoimmunotherapy induces strong immune responses and long-term survival in patients with HLA class I-deficient non-small cell lung cancer.</name><description>&lt;h4>Background&lt;/h4>Loss of human leukocyte antigen (HLA) class I expression and loss of heterozygosity (LOH) are common events implicated in the primary resistance of non-small cell lung cancer (NSCLC) to immunotherapy. However, there is no data on perioperative chemoimmunotherapy (ChIO) efficacy or response mechanisms in the context of HLA class I defects.&lt;h4>Methods&lt;/h4>Baseline HLA class I tumor status (HLA-deficient (HLA-DEF) or HLA-proficient (HLA-PRO)) was determined by DNA LOH combined with immunohistochemistry for protein levels in tissue of 24 patients with NSCLC treated with perioperative nivolumab plus chemotherapy from NADIM trial (NCT03081689). We integrated HLA tumor status with molecular data (programmed death-ligand 1 (PD-L1), TMB, TCR repertoire, TILs populations, bulk RNA</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2026-07-15T13:04:14.853Z</modification><creation>2025-04-04T22:47:44.936Z</creation></dates><accession>S-EPMC11492944</accession><cross_references><pubmed>39428126</pubmed><doi>10.1136/jitc-2024-009762</doi></cross_references></HashMap>