<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>29(10)</volume><submitter>Westin JR</submitter><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Older patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) may be considered ineligible for curative-intent therapy including high-dose chemotherapy with autologous stem-cell transplantation (HDT-ASCT). Here, we report outcomes of a preplanned subgroup analysis of patients ≥65 years in ZUMA-7.&lt;h4>Patients and methods&lt;/h4>Patients with LBCL refractory to or relapsed ≤12 months after first-line chemoimmunotherapy were randomized 1:1 to axicabtagene ciloleucel [axi-cel; autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy] or standard of care (SOC; 2-3 cycles of chemoimmunotherapy followed by HDT-ASCT). The primary endpoint was event-free survival (EFS). Secondary endpoints included safety and patient-reported outcomes (PROs).&lt;h4>Results&lt;/h4>Fift</pubmed_abstract><journal>Clinical cancer research : an official journal of the American Association for Cancer Research</journal><pagination>1894-1905</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10183830</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Safety and Efficacy of Axicabtagene Ciloleucel versus Standard of Care in Patients 65 Years of Age or Older with Relapsed/Refractory Large B-Cell Lymphoma.</pubmed_title><pmcid>PMC10183830</pmcid><pubmed_authors>Snider JT</pubmed_authors><pubmed_authors>Locke FL</pubmed_authors><pubmed_authors>Westin JR</pubmed_authors><pubmed_authors>Wulf G</pubmed_authors><pubmed_authors>Farooq U</pubmed_authors><pubmed_authors>van Meerten T</pubmed_authors><pubmed_authors>Shah J</pubmed_authors><pubmed_authors>Kersten MJ</pubmed_authors><pubmed_authors>Dickinson M</pubmed_authors><pubmed_authors>Sureda A</pubmed_authors><pubmed_authors>Cheng P</pubmed_authors><pubmed_authors>To C</pubmed_authors><pubmed_authors>Ulrickson ML</pubmed_authors><pubmed_authors>Perales MA</pubmed_authors><pubmed_authors>Jacobson CA</pubmed_authors><pubmed_authors>Filosto S</pubmed_authors><pubmed_authors>Rapoport AP</pubmed_authors><pubmed_authors>Leslie L</pubmed_authors><pubmed_authors>Oluwole OO</pubmed_authors><pubmed_authors>Wannesson L</pubmed_authors><pubmed_authors>Pagel JM</pubmed_authors><pubmed_authors>Johnston P</pubmed_authors><pubmed_authors>Ghobadi A</pubmed_authors><pubmed_authors>Elsawy M</pubmed_authors><pubmed_authors>Miklos DB</pubmed_authors><pubmed_authors>Vardhanabhuti S</pubmed_authors><pubmed_authors>Du L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Safety and Efficacy of Axicabtagene Ciloleucel versus Standard of Care in Patients 65 Years of Age or Older with Relapsed/Refractory Large B-Cell Lymphoma.</name><description>&lt;h4>Purpose&lt;/h4>Older patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL) may be considered ineligible for curative-intent therapy including high-dose chemotherapy with autologous stem-cell transplantation (HDT-ASCT). Here, we report outcomes of a preplanned subgroup analysis of patients ≥65 years in ZUMA-7.&lt;h4>Patients and methods&lt;/h4>Patients with LBCL refractory to or relapsed ≤12 months after first-line chemoimmunotherapy were randomized 1:1 to axicabtagene ciloleucel [axi-cel; autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy] or standard of care (SOC; 2-3 cycles of chemoimmunotherapy followed by HDT-ASCT). The primary endpoint was event-free survival (EFS). Secondary endpoints included safety and patient-reported outcomes (PROs).&lt;h4>Results&lt;/h4>Fift</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-05T10:55:24.059Z</modification><creation>2025-04-05T10:55:24.059Z</creation></dates><accession>S-EPMC10183830</accession><cross_references><pubmed>36999993</pubmed><doi>10.1158/1078-0432.CCR-22-3136</doi></cross_references></HashMap>