<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(24)</volume><submitter>Makita S</submitter><funding>Celgene</funding><funding>Bristol-Myers Squibb</funding><pubmed_abstract>The autologous anti-CD19 chimeric antigen receptor (CAR) T-cell product, lisocabtagene maraleucel (liso-cel), is administered at equal target doses of CD8&lt;sup>+&lt;/sup> and CD4&lt;sup>+&lt;/sup> CAR&lt;sup>+&lt;/sup> T cells. This analysis assessed safety and efficacy of liso-cel in Japanese patients with relapsed or refractory (R/R) aggressive large B-cell lymphoma (LBCL) in Cohort 3 of TRANSCEND WORLD (NCT03484702). Liso-cel (100 × 10&lt;sup>6&lt;/sup> total CAR&lt;sup>+&lt;/sup> T cells) was administered 2-7 days after lymphodepletion. The primary efficacy endpoint was objective response rate (ORR; Lugano 2014 criteria) assessed by an independent review committee. Fourteen patients were enrolled; 10 received liso-cel infusion (median time to liso-cel availability, 23 days) and were evaluable at data cutoff (medi</pubmed_abstract><journal>Cancer medicine</journal><pagination>4889-4899</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9761090</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phase 2 results of lisocabtagene maraleucel in Japanese patients with relapsed/refractory aggressive B-cell non-Hodgkin lymphoma.</pubmed_title><pmcid>PMC9761090</pmcid><pubmed_authors>Stepan L</pubmed_authors><pubmed_authors>Rettby N</pubmed_authors><pubmed_authors>Izutsu K</pubmed_authors><pubmed_authors>Ananthakrishnan R</pubmed_authors><pubmed_authors>Yamamoto G</pubmed_authors><pubmed_authors>Ogasawara K</pubmed_authors><pubmed_authors>Makita S</pubmed_authors><pubmed_authors>Asano-Mori Y</pubmed_authors><pubmed_authors>Kaji D</pubmed_authors><pubmed_authors>Schusterbauer C</pubmed_authors><pubmed_authors>Maruyama D</pubmed_authors><pubmed_authors>Hasskarl J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase 2 results of lisocabtagene maraleucel in Japanese patients with relapsed/refractory aggressive B-cell non-Hodgkin lymphoma.</name><description>The autologous anti-CD19 chimeric antigen receptor (CAR) T-cell product, lisocabtagene maraleucel (liso-cel), is administered at equal target doses of CD8&lt;sup>+&lt;/sup> and CD4&lt;sup>+&lt;/sup> CAR&lt;sup>+&lt;/sup> T cells. This analysis assessed safety and efficacy of liso-cel in Japanese patients with relapsed or refractory (R/R) aggressive large B-cell lymphoma (LBCL) in Cohort 3 of TRANSCEND WORLD (NCT03484702). Liso-cel (100 × 10&lt;sup>6&lt;/sup> total CAR&lt;sup>+&lt;/sup> T cells) was administered 2-7 days after lymphodepletion. The primary efficacy endpoint was objective response rate (ORR; Lugano 2014 criteria) assessed by an independent review committee. Fourteen patients were enrolled; 10 received liso-cel infusion (median time to liso-cel availability, 23 days) and were evaluable at data cutoff (medi</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-26T00:48:11.77Z</modification><creation>2025-04-06T09:49:36.368Z</creation></dates><accession>S-EPMC9761090</accession><cross_references><pubmed>35619325</pubmed><doi>10.1002/cam4.4820</doi></cross_references></HashMap>