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BIOMARKER:

CD19 expression + Chr t(8;21)

i
Other names: CD19, CD19 Molecule, B-Lymphocyte Surface Antigen B4, T-Cell Surface Antigen Leu-12, Differentiation Antigen CD19, B-Lymphocyte Antigen CD19, CD19 Antigen, CVID3, B4
Entrez ID:
Related biomarkers:
over1year
POINT OF CARE CD19 CHIMERIC ANTIGEN RECEPTOR (CAR) T-CELLS FOR RELAPSED/REFRACTORY ACUTE MYELOID LEUKEMIA (AML) WITH ABERRANT CD19 ANTIGEN EXPRESSION (EHA 2023)
Lymphodepletion included fludarabine and cyclophosphamide...All pts developed CRS (grade 1-3) and were treated with supported treatment and 3/6 pts received i.v tocilizumab and/or dexamethasone...Six months post-transplant the pt relapsed again, responded to azacitidine/venetoclax combination, and, was in CR for 11 months but then relapsed and died...We presented 6 pts with R/PR t (8; 21) AML with aberrant CD19 expression after multiple lines of therapies (4 post allo-SCT), treated by point of care CD19 CAR T-cells with 4 pts achieving CR. CD-19 CAR T cells administration for AML is feasible and safe. However, the response is short and should be followed by a second transplant or alternative anti leukemic therapies.
IO biomarker
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FLT3 (Fms-related tyrosine kinase 3) • IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • IDH2 (Isocitrate Dehydrogenase (NADP(+)) 2) • NPM1 (Nucleophosmin 1) • CD19 (CD19 Molecule) • RUNX1 (RUNX Family Transcription Factor 1) • RUNX1T1 (RUNX1 Partner Transcriptional Co-Repressor 1)
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FLT3-ITD mutation • CD19 expression • CD19 expression + Chr t(8;21)
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Venclexta (venetoclax) • azacitidine • cyclophosphamide • dexamethasone • fludarabine IV • Actemra IV (tocilizumab)