<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Epstein-Peterson ZD</submitter><funding>NCI NIH HHS</funding><pagination>5654-5662</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12848353</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(21)</volume><pubmed_abstract>&lt;h4>Abstract&lt;/h4>The treatment patterns and clinical outcomes for patients experiencing progression of disease (POD) following CD19-directed chimeric antigen receptor (CAR) T-cell therapy for relapsed or refractory (R/R) mantle cell lymphoma (MCL) are undefined. We identified all patients who received CD19-directed CAR T-cell therapy for R/R MCL therapy across 15 international centers, and studied those experiencing POD post-CAR T-cell therapy in detail. We extracted clinical/treatment/pathologic variables, and associated these features with survival outcomes. In total, 384 patients received CAR T-cell therapy, and 135 (35%) experienced POD. POD occurred at a median of 6 months following CAR T-cell therapy infusion, and most (64%) patients with POD had complete response as best response to</pubmed_abstract><journal>Blood advances</journal><pubmed_title>Treatment and outcomes of progression of disease post-CAR T-cell therapy in mantle cell lymphoma: a multicenter analysis.</pubmed_title><pmcid>PMC12848353</pmcid><funding_grant_id>P30 CA008748</funding_grant_id><pubmed_authors>Rhodes J</pubmed_authors><pubmed_authors>Chong EA</pubmed_authors><pubmed_authors>Shouval R</pubmed_authors><pubmed_authors>Lionel AC</pubmed_authors><pubmed_authors>Drill E</pubmed_authors><pubmed_authors>Ip A</pubmed_authors><pubmed_authors>Munoz JL</pubmed_authors><pubmed_authors>Varon B</pubmed_authors><pubmed_authors>Karmali R</pubmed_authors><pubmed_authors>Merryman RW</pubmed_authors><pubmed_authors>Kamdar MK</pubmed_authors><pubmed_authors>Zelenetz AD</pubmed_authors><pubmed_authors>Frank MJ</pubmed_authors><pubmed_authors>Sawalha Y</pubmed_authors><pubmed_authors>Riedell PA</pubmed_authors><pubmed_authors>van Besien H</pubmed_authors><pubmed_authors>Jacobson CA</pubmed_authors><pubmed_authors>Navalekar R</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Yamshon S</pubmed_authors><pubmed_authors>Palomba ML</pubmed_authors><pubmed_authors>Jain P</pubmed_authors><pubmed_authors>Beyar-Katz O</pubmed_authors><pubmed_authors>Sharma S</pubmed_authors><pubmed_authors>Maddocks KJ</pubmed_authors><pubmed_authors>Brooks TR</pubmed_authors><pubmed_authors>Sauter CS</pubmed_authors><pubmed_authors>Epstein-Peterson ZD</pubmed_authors><pubmed_authors>Matasar MJ</pubmed_authors><pubmed_authors>Shukla N</pubmed_authors><pubmed_authors>Salles G</pubmed_authors><pubmed_authors>Dela Cruz J</pubmed_authors><pubmed_authors>Ryan CE</pubmed_authors><pubmed_authors>Atallah-Yunes SA</pubmed_authors><pubmed_authors>Chong ER</pubmed_authors><pubmed_authors>Therwhanger D</pubmed_authors><pubmed_authors>McLoughlin D</pubmed_authors><pubmed_authors>Joseph A</pubmed_authors><pubmed_authors>Kumar A</pubmed_authors><pubmed_authors>Iqbal M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment and outcomes of progression of disease post-CAR T-cell therapy in mantle cell lymphoma: a multicenter analysis.</name><description>&lt;h4>Abstract&lt;/h4>The treatment patterns and clinical outcomes for patients experiencing progression of disease (POD) following CD19-directed chimeric antigen receptor (CAR) T-cell therapy for relapsed or refractory (R/R) mantle cell lymphoma (MCL) are undefined. We identified all patients who received CD19-directed CAR T-cell therapy for R/R MCL therapy across 15 international centers, and studied those experiencing POD post-CAR T-cell therapy in detail. We extracted clinical/treatment/pathologic variables, and associated these features with survival outcomes. In total, 384 patients received CAR T-cell therapy, and 135 (35%) experienced POD. POD occurred at a median of 6 months following CAR T-cell therapy infusion, and most (64%) patients with POD had complete response as best response to</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Nov</publication><modification>2026-06-14T06:07:28.451Z</modification><creation>2026-06-14T03:16:44.283Z</creation></dates><accession>S-EPMC12848353</accession><cross_references><pubmed>40763269</pubmed><doi>10.1182/bloodadvances.2025016315</doi></cross_references></HashMap>