<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu W</submitter><funding>Tianjin Municipal Science and Technology Plan Program</funding><funding>the Distinguished Young Scholars of Tianjin</funding><funding>CAMS Innovation Fund for Medical Sciences</funding><funding>National Nature Science Foundation of China</funding><funding>the Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences</funding><pagination>e008857</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11029269</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Approximately two-thirds of patients with relapsed or refractory large B-cell lymphoma (R/R LBCL) do not respond to or relapse after anti-CD19 chimeric antigen receptor T (CAR T)-cell therapy, leading to poor outcomes. Previous studies have suggested that intensified lymphodepletion and hematological stem cell infusion can promote adoptively transferred T-cell expansion, enhancing antitumor effects. Therefore, we conducted a phase I/II clinical trial in which CNCT19 (an anti-CD19 CAR T-cell) was administered after myeloablative high-dose chemotherapy and autologous stem cell transplantation (HDT/ASCT) in patients with R/R LBCL.&lt;h4>Methods&lt;/h4>Transplant-eligible patients with LBCL who were refractory to first-line immunochemotherapy or experiencing R/R status after salva</pubmed_abstract><journal>Journal for immunotherapy of cancer</journal><pubmed_title>Combinational therapy of CAR T-cell and HDT/ASCT demonstrates impressive clinical efficacy and improved CAR T-cell behavior in relapsed/refractory large B-cell lymphoma.</pubmed_title><pmcid>PMC11029269</pmcid><funding_grant_id>22JCJQJC00070</funding_grant_id><funding_grant_id>82101933</funding_grant_id><funding_grant_id>2022-I2M-1-022</funding_grant_id><funding_grant_id>2020-I2M-C&amp;amp;T-B-085</funding_grant_id><funding_grant_id>2021-RC310-011</funding_grant_id><funding_grant_id>22ZYCGSY00830</funding_grant_id><funding_grant_id>2021-I2M-1-041</funding_grant_id><funding_grant_id>2022-I2M-C&amp;amp;T-B-089</funding_grant_id><funding_grant_id>2022-RC320-01</funding_grant_id><pubmed_authors>Zou H</pubmed_authors><pubmed_authors>Liu H</pubmed_authors><pubmed_authors>Deng S</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Yi S</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Zheng W</pubmed_authors><pubmed_authors>Zou D</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Xiong W</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Shi Y</pubmed_authors><pubmed_authors>Qiu L</pubmed_authors><pubmed_authors>Lv L</pubmed_authors><pubmed_authors>Peng G</pubmed_authors><pubmed_authors>Huang W</pubmed_authors><pubmed_authors>Sui W</pubmed_authors><pubmed_authors>Lv R</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Wei J</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Combinational therapy of CAR T-cell and HDT/ASCT demonstrates impressive clinical efficacy and improved CAR T-cell behavior in relapsed/refractory large B-cell lymphoma.</name><description>&lt;h4>Background&lt;/h4>Approximately two-thirds of patients with relapsed or refractory large B-cell lymphoma (R/R LBCL) do not respond to or relapse after anti-CD19 chimeric antigen receptor T (CAR T)-cell therapy, leading to poor outcomes. Previous studies have suggested that intensified lymphodepletion and hematological stem cell infusion can promote adoptively transferred T-cell expansion, enhancing antitumor effects. Therefore, we conducted a phase I/II clinical trial in which CNCT19 (an anti-CD19 CAR T-cell) was administered after myeloablative high-dose chemotherapy and autologous stem cell transplantation (HDT/ASCT) in patients with R/R LBCL.&lt;h4>Methods&lt;/h4>Transplant-eligible patients with LBCL who were refractory to first-line immunochemotherapy or experiencing R/R status after salva</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-08T06:02:10.947Z</modification><creation>2026-06-08T03:14:14.113Z</creation></dates><accession>S-EPMC11029269</accession><cross_references><pubmed>38631712</pubmed><doi>10.1136/jitc-2024-008857</doi></cross_references></HashMap>