Abstract
B-cell acute lymphoblastic leukemia (B-ALL) is a hematologic malignancy of B-type lymphoid precursor cells. Minimal/measurable residual disease (MRD) is an important prognostic factor for B-ALL relapse. Traditional flow cytometry detection mainly relies on CD19-based gating strategies. However, relapse of CD19-negative B-ALL frequently occurs in patients who receive cellular and targeted therapy. This review will summarize the technical aspects of standard MRD assessment in B-ALL by flow cytometry, and then discuss the challenges of MRD strategies to deal with the scenario of CD19 negative or dim B-ALL relapse.
Keywords:
Acute lymphoblastic leukemia; Minimal/measurable residual disease; Targeted therapy.
MeSH terms
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Antibodies, Bispecific / therapeutic use
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Antibody Specificity
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Antigens, CD / immunology
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Antigens, CD19 / analysis
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Antigens, Neoplasm / analysis
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Antigens, Neoplasm / immunology
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Antineoplastic Agents, Immunological / immunology
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Antineoplastic Agents, Immunological / therapeutic use
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Biomarkers, Tumor
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Flow Cytometry / methods*
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Humans
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Immunophenotyping
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Immunotherapy
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Immunotherapy, Adoptive
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Molecular Targeted Therapy*
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Neoplasm, Residual
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / drug therapy
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / pathology*
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Precursor B-Cell Lymphoblastic Leukemia-Lymphoma / therapy
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Prognosis
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Sensitivity and Specificity
Substances
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Antibodies, Bispecific
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Antigens, CD
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Antigens, CD19
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Antigens, Neoplasm
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Antineoplastic Agents, Immunological
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Biomarkers, Tumor
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CD19 molecule, human
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blinatumomab