TY - JOUR
T1 - Cytopenias after cd19 chimeric antigen receptor t-cells (Car-t) therapy for diffuse large b-cell lymphomas or transformed follicular lymphoma
T2 - A single institution experience
AU - Schaefer, Andrew
AU - Huang, Ying
AU - Kittai, Adam
AU - Maakaron, Joseph E.
AU - Saygin, Caner
AU - Brammer, Jonathan
AU - Penza, Sam
AU - Saad, Ayman
AU - Jaglowski, Samantha M.
AU - William, Basem M.
N1 - Publisher Copyright:
© 2021 Schaefer et al.
PY - 2021
Y1 - 2021
N2 - Introduction: Patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) have poor outcomes. Treatment with CD19 chimeric antigen receptor (CAR-T) cells, tisa-genlecleucel and axicabtagene ciloleucel, has been associated with improved outcomes. Cytopenias were observed in clinical trials with both products; however, little is known regarding the patterns and outcomes of these cytopenias. Subjects and Methods: We reviewed DLBCL patients (n=32) receiving either product between January and September 2018 at our institution. Results: Median duration of leukopenia, neutropenia, lymphopenia, anemia, and thrombo-cytopenia was 49, 9, 117.5, 125, and 95.5 days after CAR-T infusion, respectively. Filgrastim was used in 63% of patients, and 50% of patients received red cell or platelet transfusions. With the exception of neutropenia, increase in the duration of cytopenia of any lineage was associated with improvement in progression-free survival, and in overall survival in case of anemia. There was no association between the duration of cytopenias with either cytokine release syndrome or neurotoxicity. Discussion: Our data suggest a correlation between cytopenias and survival outcomes after CD19 CAR-T therapy. If validated, cytopenia may be proven useful as a biomarker of response and survival after CAR-T therapy.
AB - Introduction: Patients with relapsed/refractory diffuse large B-cell lymphoma (DLBCL) have poor outcomes. Treatment with CD19 chimeric antigen receptor (CAR-T) cells, tisa-genlecleucel and axicabtagene ciloleucel, has been associated with improved outcomes. Cytopenias were observed in clinical trials with both products; however, little is known regarding the patterns and outcomes of these cytopenias. Subjects and Methods: We reviewed DLBCL patients (n=32) receiving either product between January and September 2018 at our institution. Results: Median duration of leukopenia, neutropenia, lymphopenia, anemia, and thrombo-cytopenia was 49, 9, 117.5, 125, and 95.5 days after CAR-T infusion, respectively. Filgrastim was used in 63% of patients, and 50% of patients received red cell or platelet transfusions. With the exception of neutropenia, increase in the duration of cytopenia of any lineage was associated with improvement in progression-free survival, and in overall survival in case of anemia. There was no association between the duration of cytopenias with either cytokine release syndrome or neurotoxicity. Discussion: Our data suggest a correlation between cytopenias and survival outcomes after CD19 CAR-T therapy. If validated, cytopenia may be proven useful as a biomarker of response and survival after CAR-T therapy.
KW - Chimeric antigen receptor T-cells
KW - Cytopenias
KW - Diffuse large B-cell lymphoma
KW - Immunotherapy
KW - Transformed follicular lymphomas
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U2 - 10.2147/CMAR.S321202
DO - 10.2147/CMAR.S321202
M3 - Article
C2 - 34876852
AN - SCOPUS:85120439274
SN - 1179-1322
VL - 13
SP - 8901
EP - 8906
JO - Cancer Management and Research
JF - Cancer Management and Research
ER -