<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(1)</volume><submitter>Zhang L</submitter><pubmed_abstract>Anti-programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) immunotherapy has dramatically changed the therapeutic landscape of inoperable non-small cell lung cancer (NSCLC), and has been included in first-line treatments. Sintilimab is a domestic anti-PD-1 monoclonal antibody in China that has received approvals from the National Medical Products Administration to treat classical Hodgkin's lymphoma, hepatocellular carcinoma, and squamous and non-squamous NSCLC. In a prospective clinical study we led, neoadjuvant sintilimab has led to major and complete pathologic responses, which are recommended as surrogate endpoints for neoadjuvant immunotherapy; however, its effect remains inconclusive in pulmonary ground glass nodules. Meanwhile, combination plans seem more likely to be satisfyin</pubmed_abstract><journal>Biomarker research</journal><pagination>23</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9014583</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Sintilimab for the treatment of non-small cell lung cancer.</pubmed_title><pmcid>PMC9014583</pmcid><pubmed_authors>He J</pubmed_authors><pubmed_authors>Xue Q</pubmed_authors><pubmed_authors>Lin W</pubmed_authors><pubmed_authors>Gao Y</pubmed_authors><pubmed_authors>Tan F</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Gao S</pubmed_authors><pubmed_authors>Li N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sintilimab for the treatment of non-small cell lung cancer.</name><description>Anti-programmed death-1 (PD-1)/programmed death-ligand 1 (PD-L1) immunotherapy has dramatically changed the therapeutic landscape of inoperable non-small cell lung cancer (NSCLC), and has been included in first-line treatments. Sintilimab is a domestic anti-PD-1 monoclonal antibody in China that has received approvals from the National Medical Products Administration to treat classical Hodgkin's lymphoma, hepatocellular carcinoma, and squamous and non-squamous NSCLC. In a prospective clinical study we led, neoadjuvant sintilimab has led to major and complete pathologic responses, which are recommended as surrogate endpoints for neoadjuvant immunotherapy; however, its effect remains inconclusive in pulmonary ground glass nodules. Meanwhile, combination plans seem more likely to be satisfyin</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T19:31:49.11Z</modification><creation>2025-02-19T02:57:40.356Z</creation></dates><accession>S-EPMC9014583</accession><cross_references><pubmed>35436956</pubmed><doi>10.1186/s40364-022-00363-7</doi></cross_references></HashMap>