B-ALL Minimal Residual Disease (MRD) Analysis
This test monitors minimal residual disease (MRD) in patients with B-cell acute lymphoblastic leukemia (B-ALL). It detects low levels of leukemic cells after treatment, helping assess the effectiveness of therapy. MRD analysis is important for predicting relapse and patient prognosis.
Overview of B-ALL Minimal Residual Disease (MRD) Analysis in Navi Mumbai
What is Minimal Residual Disease testing and why is it important?
MRD testing is a highly sensitive method used to detect small numbers of cancer cells that may remain in a patient's body after treatment, particularly in blood cancers like acute lymphoblastic leukemia (ALL) and multiple myeloma. Even if standard tests show no detectable cancer, MRD testing can uncover traces that could lead to relapse, making it a critical tool for evaluating treatment efficacy and long-term prognosis.
How is MRD testing performed?
MRD can be assessed through bone marrow or blood samples using advanced techniques such as flow cytometry, polymerase chain reaction (PCR), or next-generation sequencing (NGS). These technologies can identify one cancerous cell among tens of thousands or even a million normal cells, providing a more accurate measure of remission.
What do the results mean?
A positive MRD result indicates the presence of residual cancer cells and a higher risk of relapse, often prompting adjustments in treatment such as intensification of therapy or stem cell transplant consideration. A negative MRD result suggests a deeper remission and generally a better prognosis, although continued monitoring remains essential.
Is the MRD test part of standard cancer follow-up?
In many hematologic malignancies, MRD testing is becoming standard practice. It guides personalized treatment decisions, including de-escalation in some cases or more aggressive therapy in others. It is also used as an endpoint in clinical trials evaluating new cancer treatments.
Does MRD testing have any limitations?
While highly sensitive, MRD tests require precise timing, high-quality samples, and skilled interpretation. False negatives can occur if the disease is not uniformly distributed or if the markers used for detection are no longer present. Coordination with a hematologist or oncologist is essential for accurate assessment and action.
Test included
- B-all Mrd
- Comments
- Advised
- Immunophenotype At Presentation
- Stage Of Chemotherapy
- Instrument/software Used
- Cell Preparation Method
- Reagent Panel Applied
- Gating Strategy
- Sample Type
- Sample Collection Date
- Sample Analysis Time
- Total Events Acquired
- Total Nucleated Cell Events Acquired
- Cd19 Positive Events
- B-all Events
- B-all Residual Blasts
- Additional Markers Tested
Doctor information
Test code
7618
CPT and Loinc codes
Department
- Flow Cytometry
Turn around time
3 Working Days
Performing locations
2 labs across India
Specimen vol. and vacutainer information
| Specimen | Vacutainer | Volume |
|---|---|---|
| Bone Marrow | Others | 2 ML |
| Bone Marrow Heparin | Green Vacutainer | |
| Bone Marrow Smear | Slider Mail Box | |
| Edta Whole Blood | Lavender Vacutainer | 2 ML |
| Heparin Whole Blood | Green Vacutainer | 2 ML |
Specimen stability information
Bone Marrow, Bone Marrow Heparin, Bone Marrow Smear
Collection instructions
2-3 unfixed, unstained direct smears, sample to reach laboratory preferably within 24 hrs of collection. Filled history sheet, initial Immunophenotyping report/data and Flow Cytometry scatter plots reported at the time of diagnosis/presentation shall be sent along with sample and day post chemotherapy.
Package price
₹11235
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₹11235