<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ahmed N</submitter><funding>NIEHS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>5382-5396</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12597645</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(20)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>Brexucabtagene autoleucel (brexu-cel) is a chimeric antigen receptor T-cell therapy approved for relapsed/refractory mantle cell lymphoma (R/R MCL). Here, we report real-world effectiveness and safety outcomes of brexu-cel in a prospective study of patients with R/R MCL, including subgroups based on prior treatment with Bruton's tyrosine kinase inhibitor, bendamustine, or autologous hematopoietic cell transplant (auto-HCT) and number of prior therapy lines, using Center for International Blood and Marrow Transplant Research registry data. A total of 476 patients with R/R MCL who received brexu-cel between July 2020 and December 2022 were included in the analysis. With a median follow-up of 13.5 months, the overall response rate was 91% and complete response rate was 82%. O</pubmed_abstract><journal>Blood advances</journal><pubmed_title>Real-world outcomes of brexucabtagene autoleucel for relapsed or refractory mantle cell lymphoma: a CIBMTR analysis.</pubmed_title><pmcid>PMC12597645</pmcid><funding_grant_id>27398C0011</funding_grant_id><funding_grant_id>U24 CA233032</funding_grant_id><funding_grant_id>U24 CA076518</funding_grant_id><funding_grant_id>27305C0011</funding_grant_id><funding_grant_id>27307C0011</funding_grant_id><pubmed_authors>Locke FL</pubmed_authors><pubmed_authors>Ahmed S</pubmed_authors><pubmed_authors>Thiruvengadam SK</pubmed_authors><pubmed_authors>Dalton D</pubmed_authors><pubmed_authors>Lee D</pubmed_authors><pubmed_authors>Herrera AF</pubmed_authors><pubmed_authors>Ahmed N</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Kharfan-Dabaja MA</pubmed_authors><pubmed_authors>Gerson J</pubmed_authors><pubmed_authors>Kloos I</pubmed_authors><pubmed_authors>Shadman M</pubmed_authors><pubmed_authors>Frank MJ</pubmed_authors><pubmed_authors>Budde LE</pubmed_authors><pubmed_authors>Turtle CJ</pubmed_authors><pubmed_authors>Grover N</pubmed_authors><pubmed_authors>Bye M</pubmed_authors><pubmed_authors>Sauter C</pubmed_authors><pubmed_authors>Pasquini MC</pubmed_authors><pubmed_authors>Xu H</pubmed_authors><pubmed_authors>Hu ZH</pubmed_authors><pubmed_authors>Logan B</pubmed_authors><pubmed_authors>Kim S</pubmed_authors><pubmed_authors>Hamadani M</pubmed_authors><pubmed_authors>Hematti P</pubmed_authors><pubmed_authors>Nunes A</pubmed_authors><pubmed_authors>Moskop A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Real-world outcomes of brexucabtagene autoleucel for relapsed or refractory mantle cell lymphoma: a CIBMTR analysis.</name><description>&lt;h4>Abstract&lt;/h4>Brexucabtagene autoleucel (brexu-cel) is a chimeric antigen receptor T-cell therapy approved for relapsed/refractory mantle cell lymphoma (R/R MCL). Here, we report real-world effectiveness and safety outcomes of brexu-cel in a prospective study of patients with R/R MCL, including subgroups based on prior treatment with Bruton's tyrosine kinase inhibitor, bendamustine, or autologous hematopoietic cell transplant (auto-HCT) and number of prior therapy lines, using Center for International Blood and Marrow Transplant Research registry data. A total of 476 patients with R/R MCL who received brexu-cel between July 2020 and December 2022 were included in the analysis. With a median follow-up of 13.5 months, the overall response rate was 91% and complete response rate was 82%. O</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-05T12:29:29.893Z</modification><creation>2026-05-16T03:12:23.396Z</creation></dates><accession>S-EPMC12597645</accession><cross_references><pubmed>40706035</pubmed><doi>10.1182/bloodadvances.2024015014</doi></cross_references></HashMap>