<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma S</submitter><funding>National Natural Science Foundation of China</funding><pagination>104</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11024067</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>73(6)</volume><pubmed_abstract>Few studies have reported the associations of granulocyte colony-stimulating factor (G-CSF) with cytokine release syndrome (CRS), neurotoxic events (NEs) and efficacy after chimeric antigen receptor (CAR) T-cell therapy for relapsed or refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL). We present a retrospective study of 67 patients with R/R B-ALL who received anti-CD19 CAR T-cell therapy, 41 (61.2%) patients received G-CSF (G-CSF group), while 26 (38.8%) did not (non-G-CSF group). Patients had similar duration of grade 3-4 neutropenia between the two groups. The incidences of CRS and NEs were higher in G-CSF group, while no differences in severity were found. Further stratified analysis showed that the incidence and severity of CRS were not associated with G-CSF administration </pubmed_abstract><journal>Cancer immunology, immunotherapy : CII</journal><pubmed_title>Associations of granulocyte colony-stimulating factor with toxicities and efficacy of chimeric antigen receptor T-cell therapy in relapsed or refractory B-cell acute lymphoblastic leukemia.</pubmed_title><pmcid>PMC11024067</pmcid><funding_grant_id>82270232</funding_grant_id><pubmed_authors>Xu K</pubmed_authors><pubmed_authors>Ma S</pubmed_authors><pubmed_authors>Lu W</pubmed_authors><pubmed_authors>Qi K</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Cao J</pubmed_authors><pubmed_authors>Zhu F</pubmed_authors><pubmed_authors>Sang W</pubmed_authors><pubmed_authors>Zhao M</pubmed_authors><pubmed_authors>Yan Z</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Qi Y</pubmed_authors><pubmed_authors>Niu M</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Cheng H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Associations of granulocyte colony-stimulating factor with toxicities and efficacy of chimeric antigen receptor T-cell therapy in relapsed or refractory B-cell acute lymphoblastic leukemia.</name><description>Few studies have reported the associations of granulocyte colony-stimulating factor (G-CSF) with cytokine release syndrome (CRS), neurotoxic events (NEs) and efficacy after chimeric antigen receptor (CAR) T-cell therapy for relapsed or refractory (R/R) B-cell acute lymphoblastic leukemia (B-ALL). We present a retrospective study of 67 patients with R/R B-ALL who received anti-CD19 CAR T-cell therapy, 41 (61.2%) patients received G-CSF (G-CSF group), while 26 (38.8%) did not (non-G-CSF group). Patients had similar duration of grade 3-4 neutropenia between the two groups. The incidences of CRS and NEs were higher in G-CSF group, while no differences in severity were found. Further stratified analysis showed that the incidence and severity of CRS were not associated with G-CSF administration </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2025-04-22T20:48:27.226Z</modification><creation>2025-04-06T03:17:03.852Z</creation></dates><accession>S-EPMC11024067</accession><cross_references><pubmed>38630258</pubmed><doi>10.1007/s00262-024-03661-1</doi></cross_references></HashMap>