Related Experiment Video
Updated: Jun 11, 2025

09:01
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
13.9K
Classification and risk stratification in T-lineage acute lymphoblastic leukemia
Petri Pölönen1, Charles G Mullighan1, David T Teachey2,3
1Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN.
Blood
|October 2, 2024
Summary
Risk stratification for acute lymphoblastic leukemia (ALL) is improving, but T-ALL remains challenging. Recent genomic profiling identifies new biomarkers to guide T-ALL treatment and improve patient outcomes.
Area of Science:
- Hematology
- Oncology
- Genetics
Background:
- Acute lymphoblastic leukemia (ALL) cure rates have significantly improved due to risk stratification.
- While effective for B-lineage ALL, risk stratification for T-lineage ALL (T-ALL) remains a challenge.
- Established T-ALL prognostic factors include age, CNS involvement, and MRD response.
Purpose of the Study:
- To review current challenges in T-ALL risk stratification.
- To highlight recent advances in identifying prognostic biomarkers for T-ALL.
- To underscore the potential of genomics in guiding future T-ALL treatment.
Main Methods:
- Review of clinical trials and real-world data in T-ALL.
- Analysis of immunophenotype and its association with T-ALL outcomes.
- Incorporation of recent large-scale genomic profiling data.
Main Results:
- Genomic profiling has identified multiple genetic subtypes and alterations in T-ALL.
- These genetic alterations are associated with outcomes independent of measurable residual disease (MRD).
- Immunophenotype, while used for classification, lacks consistent association with T-ALL outcomes in multivariable models.
Conclusions:
- Genomic classification holds significant potential for guiding future T-ALL treatment strategies.
- Ongoing efforts focus on identifying reliable prognostic biomarkers for T-ALL.
- Advances in genomics are crucial for refining risk stratification and improving T-ALL patient care.
Related Concept Videos
Lineage Commitment
3.0K
Commitment is the process whereby stem cells:
3.0K
Classification of Leukocytes
1.7K
Leukocytes are classified into two groups based on the presence or absence of cytoplasmic granules. Granular leukocytes, which contain granules, belong to the myeloid lineage and are divided into three subtypes: neutrophils, eosinophils, and basophils. These cells are roughly spherical and characterized by the granules in their cytoplasm.
Neutrophils are the most abundant type of granular leukocytes, comprising 50-70% of all leukocytes. They feature small, evenly distributed granules and a...
Neutrophils are the most abundant type of granular leukocytes, comprising 50-70% of all leukocytes. They feature small, evenly distributed granules and a...
1.7K
Disorders of Leukocytes
902
Leukocyte disorders can lead to either leukopenia, characterized by an abnormally low leukocyte count, or leukocytosis, marked by a very high leukocyte number.
Leukopenia may result from bone marrow disorders, autoimmune diseases, and infectious diseases. For example, conditions such as multiple myeloma and aplastic anemia can impair the bone marrow's ability to produce adequate leukocytes. Similarly, autoimmune diseases like lupus and viral infections such as HIV can prompt the immune...
Leukopenia may result from bone marrow disorders, autoimmune diseases, and infectious diseases. For example, conditions such as multiple myeloma and aplastic anemia can impair the bone marrow's ability to produce adequate leukocytes. Similarly, autoimmune diseases like lupus and viral infections such as HIV can prompt the immune...
902

