<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(12)</volume><submitter>Shankar B</submitter><pubmed_abstract>&lt;h4>Importance&lt;/h4>The spectrum of individual immune-related adverse events (irAEs) from anti-programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) immune checkpoint inhibitors (ICIs) has been reported widely, and their development is associated with improved patient survival across tumor types. The spectrum and impact on survival for patients with non-small cell lung cancer (NSCLC) who develop multisystem irAEs from ICIs, has not been described.&lt;h4>Objective&lt;/h4>To characterize multisystem irAEs, their association with survival, and risk factors for multisystem irAE development.&lt;h4>Design, setting, and participants&lt;/h4>This retrospective cohort study carried out in 5 academic institutions worldwide included 623 patients with stage III/IV NSCLC, treated with anti-PD-(L)</pubmed_abstract><journal>JAMA oncology</journal><pagination>1952-1956</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7596677</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multisystem Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitors for Treatment of Non-Small Cell Lung Cancer.</pubmed_title><pmcid>PMC7596677</pmcid><pubmed_authors>Sugawara S</pubmed_authors><pubmed_authors>Otterson GA</pubmed_authors><pubmed_authors>Naidoo J</pubmed_authors><pubmed_authors>Brahmer JR</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Feliciano JL</pubmed_authors><pubmed_authors>Patel SH</pubmed_authors><pubmed_authors>Walker P</pubmed_authors><pubmed_authors>Forde PM</pubmed_authors><pubmed_authors>Naqash AR</pubmed_authors><pubmed_authors>Shankar B</pubmed_authors><pubmed_authors>Ricciuti B</pubmed_authors><pubmed_authors>Marrone KA</pubmed_authors><pubmed_authors>Toi Y</pubmed_authors><pubmed_authors>Hann CL</pubmed_authors><pubmed_authors>Ettinger DS</pubmed_authors><pubmed_authors>Owen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multisystem Immune-Related Adverse Events Associated With Immune Checkpoint Inhibitors for Treatment of Non-Small Cell Lung Cancer.</name><description>&lt;h4>Importance&lt;/h4>The spectrum of individual immune-related adverse events (irAEs) from anti-programmed cell death 1 (PD-1) and programmed cell death ligand 1 (PD-L1) immune checkpoint inhibitors (ICIs) has been reported widely, and their development is associated with improved patient survival across tumor types. The spectrum and impact on survival for patients with non-small cell lung cancer (NSCLC) who develop multisystem irAEs from ICIs, has not been described.&lt;h4>Objective&lt;/h4>To characterize multisystem irAEs, their association with survival, and risk factors for multisystem irAE development.&lt;h4>Design, setting, and participants&lt;/h4>This retrospective cohort study carried out in 5 academic institutions worldwide included 623 patients with stage III/IV NSCLC, treated with anti-PD-(L)</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Dec</publication><modification>2025-04-04T14:15:10.029Z</modification><creation>2025-04-04T14:15:10.029Z</creation></dates><accession>S-EPMC7596677</accession><cross_references><pubmed>33119034</pubmed><doi>10.1001/jamaoncol.2020.5012</doi></cross_references></HashMap>