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Updated: Apr 28, 2026

Flow Cytometry to Estimate Leukemia Stem Cells in Primary Acute Myeloid Leukemia and in Patient-derived-xenografts, at Diagnosis and Follow Up
Published on: March 26, 2018
Immunophenotypic Heterogeneity and Clonal Sweep in Acute Myeloid Leukemia Revealed by Flow Cytometry: A Case Series
Angela Bertolini1, Marisa Gorrese1, Serena Luponio1
1Hematology and Transplant Center, University Hospital "San Giovanni di Dio e Ruggi d'Aragona", 84131 Salerno, Italy.
Flow cytometry reveals complex clonal heterogeneity in acute myeloid leukemia (AML), identifying small phenotypic subclones missed by molecular profiling. These subclones predict poorer survival, suggesting a new prognostic factor for AML.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Clonal evolution in acute myeloid leukemia (AML) is typically defined by mutations and cytogenetic changes.
- Limited research has explored immunophenotypic heterogeneity via flow cytometry and its impact on AML progression.
Purpose of the Study:
- To investigate immunophenotypic heterogeneity in AML using flow cytometry.
- To identify phenotypic subclones and assess their relationship with disease progression and survival.
Main Methods:
- Flow cytometry immunophenotyping was performed on 24 AML patients.
- Phenotypic profiles were correlated with molecular alterations detected by next-generation sequencing.
Main Results:
- Flow cytometry identified more complex clonal heterogeneity than molecular profiling at diagnosis and relapse.
- Small phenotypic subclones, undetectable by molecular methods, were identified and some expanded over time.
- The presence of small clones correlated with shorter progression-free and overall survival.
Conclusions:
- Flow cytometric clonal heterogeneity, particularly small clones (2-30% antigen expression), offers a novel prognostic factor in AML.
- Integrating immunophenotyping with molecular data can enhance risk stratification and personalized monitoring for AML patients.
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