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Published on: June 6, 2025
Immunophenotypic, cytogenetic and clinical features of 192 AML patients in China
Haixia Tong1, Chunwei Lu, Jihong Zhang
1Laboratory of Hematology, Shengjing Hospital of China Medical University, Tiexi District, 110022 Shenyang, China. tonghaixia18@yahoo.com.cn
Insights
Immunophenotypic analysis aids in diagnosing and classifying acute myeloid leukemia (AML). Specific antigen expressions correlate with AML subtypes and abnormal cytogenetic changes, improving patient stratification.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Immunophenotypic characterization is crucial for diagnosing, classifying, and determining the prognosis of leukemia.
- Flow cytometry using monoclonal antibodies is a standard method for this analysis.
Purpose of the Study:
- To investigate the utility of immunophenotyping in the diagnosis and classification of acute myeloid leukemia (AML) in a Chinese population.
- To correlate immunophenotypic findings with cytogenetic abnormalities and clinical features.
Main Methods:
- Immunophenotyping by flow cytometry was performed on 192 Chinese AML patients using a panel of monoclonal antibodies.
- Karyotype analysis by G-banding was conducted on 125 of these patients.
Main Results:
- CD33, CD13, MPO, and CD117 were the most frequently expressed antigens in AML.
- Specific antigen combinations were identified for diagnosing M3 and M5 subtypes.
- Lymphoid markers (CD56, CD7) were expressed in 47.9% of cases, with higher CD34 positivity in the lymphoid antigen-positive group.
- Abnormal karyotypes were detected in 60.8% of cases.
Conclusions:
- Immunophenotype analysis is valuable for AML diagnosis and classification.
- Immunophenotypic profiles correlate with abnormal cytogenetic changes and clinical features in AML patients.
Abstract:
Immunophenotypic characterization of the leukemic cells has been widely used as a tool for diagnosis, classification and prognosis of leukaemia. A total of 192 Chinese patients with acute myeloid leukemia (AML) were immunophenotyped by flow cytometry using a panel of monoclonal antibodies. Among the 192 patients enrolled in this study, 125 cases were also subjected to karyotype analysis by G-banding technology. We found that CD33, CD13, MPO and CD117 were the most commonly expressed antigens in AML. A combination of intensive autofluorescence, both CD34(-) and HLA-DR(-), and high expression of CD13, CD33 and MPO had significant value for M3 diagnosis. CD14 was expressed only in M4 and M5, and both intensive positivity of CD64 and CD15 with high expression of HLA-DR may suggest great possibility for diagnosis of M5. Lymphoid markers expression was documented in 47.9% of the 192 AML cases analyzed. CD56 (26.0%) and CD7 (20.8%) were the most commonly expressed lymphoid markers in AML patients. Abnormal karyotypes were detected in 76 out of 125 (60.8%). Higher CD34 positivity was found in LymAg(+) group (77.2%) than in LymAg(-) group (48.0%). Our results indicate that immunophenotype analysis was useful for AML diagnosis and classification and the immunophenotype did have relevance to the abnormal cytogenetic changes and clinical features in AML.
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