<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Riedell PA</submitter><funding>NCATS NIH HHS</funding><funding>NCI NIH HHS</funding><pagination>669-676</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9547952</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(10)</volume><pubmed_abstract>Axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are CD19-directed chimeric antigen receptor (CAR) T cell therapies approved for the treatment of relapsed/refractory aggressive B cell lymphomas. We present a multicenter retrospective study among centers that prescribe either commercial product to evaluate usage patterns, safety and efficacy outcomes, and resource utilization. Data collection included all patients from 8 US centers who underwent apheresis between May 1, 2018, and July 31, 2019. Patient selection, toxicity management, and disease assessment followed institutional practices. Cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were graded according to American Society for Transplantation and Cellular Therapy conse</pubmed_abstract><journal>Transplantation and cellular therapy</journal><pubmed_title>Patterns of Use, Outcomes, and Resource Utilization among Recipients of Commercial Axicabtagene Ciloleucel and Tisagenlecleucel for Relapsed/Refractory Aggressive B Cell Lymphomas.</pubmed_title><pmcid>PMC9547952</pmcid><funding_grant_id>UL1 TR002494</funding_grant_id><funding_grant_id>P30 CA008748</funding_grant_id><pubmed_authors>Bachanova V</pubmed_authors><pubmed_authors>Schachter L</pubmed_authors><pubmed_authors>Schuster SJ</pubmed_authors><pubmed_authors>Pennisi M</pubmed_authors><pubmed_authors>Flores OA</pubmed_authors><pubmed_authors>Hwang WT</pubmed_authors><pubmed_authors>Ahmed N</pubmed_authors><pubmed_authors>Oluwole OO</pubmed_authors><pubmed_authors>Brower J</pubmed_authors><pubmed_authors>McGuirk JP</pubmed_authors><pubmed_authors>Bharucha K</pubmed_authors><pubmed_authors>Riedell PA</pubmed_authors><pubmed_authors>Maziarz RT</pubmed_authors><pubmed_authors>Perales MA</pubmed_authors><pubmed_authors>Porter DL</pubmed_authors><pubmed_authors>Bishop MR</pubmed_authors><pubmed_authors>Nastoupil LJ</pubmed_authors><pubmed_authors>Dholaria BR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Patterns of Use, Outcomes, and Resource Utilization among Recipients of Commercial Axicabtagene Ciloleucel and Tisagenlecleucel for Relapsed/Refractory Aggressive B Cell Lymphomas.</name><description>Axicabtagene ciloleucel (axi-cel) and tisagenlecleucel (tisa-cel) are CD19-directed chimeric antigen receptor (CAR) T cell therapies approved for the treatment of relapsed/refractory aggressive B cell lymphomas. We present a multicenter retrospective study among centers that prescribe either commercial product to evaluate usage patterns, safety and efficacy outcomes, and resource utilization. Data collection included all patients from 8 US centers who underwent apheresis between May 1, 2018, and July 31, 2019. Patient selection, toxicity management, and disease assessment followed institutional practices. Cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS) were graded according to American Society for Transplantation and Cellular Therapy conse</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Oct</publication><modification>2026-05-29T14:04:42.475Z</modification><creation>2025-04-04T03:00:34.938Z</creation></dates><accession>S-EPMC9547952</accession><cross_references><pubmed>35850429</pubmed><doi>10.1016/j.jtct.2022.07.011</doi></cross_references></HashMap>