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Flow Cytometric MRD Detection in Selected Mature B-Cell Malignancies
Robby Engelmann1, Sebastian Böttcher2
1Rostock University Medical Center, Division of Internal Medicine, Medical Clinic III - Hematology, Oncology and Palliative Medicine, Special Hematology Laboratory, Rostock, Germany.
Methods in Molecular Biology (Clifton, N.J.)
|October 18, 2024
Summary
Flow cytometry standardization is crucial for accurately measuring minimal residual disease (MRD) in blood cancers. This method offers prognostic insights for mature B-cell malignancies like chronic lymphocytic leukemia and multiple myeloma.
Area of Science:
- Hematology
- Immunology
- Clinical Diagnostics
Background:
- Minimal residual disease (MRD) quantification post-therapy shows prognostic value in mature B-cell malignancies.
- Advancements in flow cytometry, including multi-color analysis and standardization, position it as a preferred MRD assessment tool for certain lymphomas.
Purpose of the Study:
- To outline general principles of flow cytometry standardization for MRD detection.
- To illustrate technical standardization strategies using chronic lymphocytic leukemia (CLL) and multiple myeloma (MM) as examples.
- To focus on MRD data acquisition and analysis in MM and CLL based on EuroFlow strategies.
Main Methods:
- Description of general aspects of flow cytometric standardization.
- Application of EuroFlow strategies for technical standardization in MRD detection.
- Detailed explanation of MRD data acquisition and analysis protocols for CLL and MM.
Main Results:
- Standardization of flow cytometry enables reliable MRD quantification.
- EuroFlow strategies provide a framework for consistent MRD assessment.
- Specific protocols for MM and CLL facilitate accurate MRD detection and analysis.
Conclusions:
- Standardized flow cytometry is essential for reliable MRD assessment in B-cell malignancies.
- The described methods and strategies enhance the prognostic significance of MRD detection.
- This approach supports improved patient management and therapeutic strategies in CLL and MM.

