Ontology highlight
ABSTRACT: Background
Measurement of minimal/measurable residual disease (MRD) in B-lymphoblastic leukemia/lymphoma (B-ALL) has become a routine clinical evaluation tool and remains the strongest predictor of treatment outcome. In recent years, new targeted anti-CD19 and anti-CD22 antibody-based and cellular therapies have revolutionized the treatment of the high-risk B-ALL. The new treatments raise challenges for diagnostic flow cytometry, which relies on the presence of specific surface antigens to identify the population of interest. So far, reported flow cytometry-based assays are developed to either achieve a deeper MRD level or to accommodate the loss of surface antigens post-target therapies, but not both.Methods
We developed a single tube flow cytometry assay (14-color-16-para
SUBMITTER: Gao Q
PROVIDER: S-EPMC10508218 | biostudies-literature | 2023 Jul
REPOSITORIES: biostudies-literature