Identifying Leukemia-associated Immunophenotypes in Acute Myeloid Leukemia Patients Using Multiparameter Flow
Hadeer Mohamed Rasheed1, Hanaa Mahmoud Donia1, Eman Attia Nadwan2
1Clinical Pathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Leukemia-associated immunophenotypes (LAIPs) were identified in 86% of acute myeloid leukemia (AML) patients using multiparameter flow cytometry. Specific LAIP combinations improve minimal residual disease detection, aiding prognosis in AML.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Acute myeloid leukemia (AML) is a heterogeneous hematologic malignancy.
- Accurate immunophenotyping is crucial for AML diagnosis and monitoring.
- Leukemia-associated immunophenotypes (LAIPs) can serve as diagnostic and prognostic markers.
Purpose of the Study:
- To identify LAIPs in AML patients at diagnosis using an eight-color multiparameter flow cytometry (MFC) panel.
- To assess alterations in LAIPs in relapsed or refractory AML cases.
- To optimize LAIP selection for enhanced minimal residual disease (MRD) detection.
Main Methods:
- Utilized an eight-color MFC panel with CD45/side scatter log gating.
- Analyzed bone marrow samples from 50 AML patients at diagnosis and relapse/refractory stages.
- Included 20 control bone marrow samples from non-malignant hematological conditions.
Main Results:
- LAIPs were detected in 86% of AML patients.
- Most patients (90.7%) exhibited 2-12 aberrant immunophenotypes.
- Specific combinations (e.g., CD2/CD4/CD56 with CD34 or CD117) yielded strong LAIPs.
- Refractory cases maintained similar LAIPs; one case showed new LAIPs upon relapse.
Conclusions:
- LAIP specificity is more critical than frequency for diagnostic utility.
- Optimized LAIP strategies enhance MFC sensitivity for MRD detection in AML.
- Accurate MRD assessment via MFC is vital for AML prognosis and clinical management.
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