<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Shah BD</submitter><funding>NCI NIH HHS</funding><pagination>491-502</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11613962</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>398(10299)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Despite treatment with novel therapies and allogeneic stem-cell transplant (allo-SCT) consolidation, outcomes in adult patients with relapsed or refractory B-precursor acute lymphoblastic leukaemia remain poor, underlining the need for more effective therapies.&lt;h4>Methods&lt;/h4>We report the pivotal phase 2 results of ZUMA-3, an international, multicentre, single-arm, open-label study evaluating the efficacy and safety of the autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy KTE-X19 in adult patients with relapsed or refractory B-precursor acute lymphoblastic leukaemia. Patients were enrolled at 25 sites in the USA, Canada, and Europe. Eligible patients were aged 18 years or older, with Eastern Cooperative Oncology Group performance status of 0-1, and mor</pubmed_abstract><journal>Lancet (London, England)</journal><pubmed_title>KTE-X19 for relapsed or refractory adult B-cell acute lymphoblastic leukaemia: phase 2 results of the single-arm, open-label, multicentre ZUMA-3 study.</pubmed_title><pmcid>PMC11613962</pmcid><funding_grant_id>P30 CA016672</funding_grant_id><pubmed_authors>Schiller GJ</pubmed_authors><pubmed_authors>Tzachanis D</pubmed_authors><pubmed_authors>Minnema MC</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Houot R</pubmed_authors><pubmed_authors>DeAngelo DJ</pubmed_authors><pubmed_authors>Feng C</pubmed_authors><pubmed_authors>Dong J</pubmed_authors><pubmed_authors>Topp MS</pubmed_authors><pubmed_authors>Abedi M</pubmed_authors><pubmed_authors>Shen T</pubmed_authors><pubmed_authors>Jeyakumar D</pubmed_authors><pubmed_authors>Baer MR</pubmed_authors><pubmed_authors>Masouleh BK</pubmed_authors><pubmed_authors>Rossi JM</pubmed_authors><pubmed_authors>Leguay T</pubmed_authors><pubmed_authors>Park JH</pubmed_authors><pubmed_authors>Shah BD</pubmed_authors><pubmed_authors>Boissel N</pubmed_authors><pubmed_authors>Logan AC</pubmed_authors><pubmed_authors>Subklewe M</pubmed_authors><pubmed_authors>O'Dwyer KM</pubmed_authors><pubmed_authors>Oluwole OO</pubmed_authors><pubmed_authors>Stiff P</pubmed_authors><pubmed_authors>Ghobadi A</pubmed_authors><pubmed_authors>Cassaday RD</pubmed_authors><pubmed_authors>Bishop MR</pubmed_authors><pubmed_authors>Wierda WG</pubmed_authors><pubmed_authors>Milletti F</pubmed_authors><pubmed_authors>Vezan R</pubmed_authors><pubmed_authors>Arellano ML</pubmed_authors></additional><is_claimable>false</is_claimable><name>KTE-X19 for relapsed or refractory adult B-cell acute lymphoblastic leukaemia: phase 2 results of the single-arm, open-label, multicentre ZUMA-3 study.</name><description>&lt;h4>Background&lt;/h4>Despite treatment with novel therapies and allogeneic stem-cell transplant (allo-SCT) consolidation, outcomes in adult patients with relapsed or refractory B-precursor acute lymphoblastic leukaemia remain poor, underlining the need for more effective therapies.&lt;h4>Methods&lt;/h4>We report the pivotal phase 2 results of ZUMA-3, an international, multicentre, single-arm, open-label study evaluating the efficacy and safety of the autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy KTE-X19 in adult patients with relapsed or refractory B-precursor acute lymphoblastic leukaemia. Patients were enrolled at 25 sites in the USA, Canada, and Europe. Eligible patients were aged 18 years or older, with Eastern Cooperative Oncology Group performance status of 0-1, and mor</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-06-03T00:58:02.201Z</modification><creation>2025-04-06T22:27:11.88Z</creation></dates><accession>S-EPMC11613962</accession><cross_references><pubmed>34097852</pubmed><doi>10.1016/s0140-6736(21)01222-8</doi><doi>10.1016/S0140-6736(21)01222-8</doi></cross_references></HashMap>