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Updated: Jun 6, 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
Acute myeloid leukemia stem cells: seek and destroy
1Weill Medical College of Cornell University, The New York Presbyterian Hospital, 520 East 70th Street, New York, NY 10021, USA. gar2001@med.cornell.edu
Most adult patients with acute myeloid leukemia (AML) die from their disease, often due to relapses. Research suggests leukemic stem cells (LSCs) drive AML and its recurrence, necessitating new therapeutic strategies.
Area of Science:
- Hematology
- Oncology
- Cancer Biology
Background:
- Acute myeloid leukemia (AML) remains a fatal disease for most adult patients.
- Frequent relapses occur despite intensive chemotherapy and stem cell transplantation.
- AML exhibits significant biological heterogeneity, including genetic mutations and molecular aberrations.
Purpose of the Study:
- To review current research on leukemic stem cells (LSCs) in AML.
- To discuss the role of LSCs in disease persistence and relapse.
- To guide the development of novel therapeutics and clinical trials targeting LSCs.
Main Methods:
- Review of bench and translational research findings on LSCs.
- Analysis of the biological characteristics of LSCs, including self-renewal and differentiation capabilities.
- Synthesis of data to inform future therapeutic strategies.
Main Results:
- Evidence suggests AML originates from a rare population of LSCs.
- LSCs possess self-renewal and differentiation potential.
- LSCs may persist post-treatment, leading to disease relapse.
Conclusions:
- LSCs are critical drivers of AML pathogenesis and relapse.
- Targeting LSCs offers a promising avenue for improving AML treatment outcomes.
- Future AML therapeutics and clinical trials should focus on LSC-directed strategies.
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09:57Comprehensive Protocol to Sample and Process Bone Marrow for Measuring Measurable Residual Disease and Leukemic Stem Cells in Acute Myeloid Leukemia
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