Minimal Residual Disease (MRD) & Disease Monitoring
After treatment, some cancers may leave behind a small number of abnormal cells that cannot be detected by routine examination. Specialized laboratory techniques can be used in selected hematological malignancies to detect minimal residual disease (MRD).
MRD testing may help clinicians assess treatment response and monitor disease status in appropriate patients, offering a level of sensitivity beyond what conventional morphological examination can achieve.
At National Path Lab (NPL), MRD assessment using flow cytometry and molecular/PCR-based methods is available for selected hematological malignancies.
- Tests available
- 5
- Tests available
- Health packages
- 2
- Health packages
Tests Available at NPL
MEASURABLE RESIDUAL DISEASE MONITORING FOR ACUTE MYELOID LEUKEMIA (AML MRD)
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 7-10 DAYS
Rs. 24000
BCR-ABL QUANTITATIVE, MRD MONITOR
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 7 DAYS
Rs. 11500
MINIMAL RESIDUAL DISEASE (MRD) MONITORING FOR MULTIPLE MYELOMA
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 7 DAYS
Rs. 22000
MINIMAL RESIDUAL DISEASE (MRD) ANALYSIS FOR B- ALL
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7-10 DAYS
Rs. 19000
MINIMAL RESIDUAL DISEASE (MRD) ANALYSIS FOR T-ALL
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 10 DAY
Rs. 24000
About Minimal Residual Disease (MRD) & Disease Monitoring
Causes & Risk Factors
MRD testing is considered at specific points in a treatment and monitoring pathway, rather than being prompted by risk factors:
• Following induction or consolidation treatment for certain leukemias, to assess depth of response
• As part of scheduled monitoring during and after treatment for selected hematological malignancies
• When assessing whether a patient remains in remission or whether disease is beginning to reappear
• To help guide decisions about treatment duration, intensity, or the need for additional therapy
Symptoms & When to Test
MRD testing is a monitoring tool used in patients with a known, previously diagnosed hematological malignancy — it is not driven by new symptoms, though the disease itself may cause symptoms if MRD progresses to overt relapse.
• Performed as scheduled monitoring in patients with known hematological malignancy under treatment or in remission
• Not typically used as a first-line diagnostic test in a person without a prior diagnosis
• A rising MRD level, without necessarily causing symptoms, may prompt closer monitoring or treatment adjustment by your hematologist
When Should You Consider Testing?
MRD testing timing is determined by your treating hematologist as part of your specific treatment protocol and monitoring schedule, typically at defined milestones during and after treatment for the relevant hematological malignancy.
Why Tests Are Combined
Different MRD techniques offer different sensitivity and are suited to different diseases — flow cytometry identifies residual abnormal cells based on their surface marker profile, while molecular and PCR-based methods can detect residual disease at a much lower level by identifying specific genetic markers unique to the patient's original malignancy.
The choice of technique depends on the specific hematological malignancy and what genetic or immunophenotypic marker was identified at original diagnosis — MRD testing generally requires that a trackable marker was established at diagnosis, which is one reason thorough initial diagnostic testing (including flow cytometry and molecular studies) matters beyond just confirming the diagnosis.
Because MRD testing is far more sensitive than routine blood counts or bone marrow morphology, it can detect very low levels of residual disease that would otherwise go unnoticed — informing treatment decisions earlier than would otherwise be possible.
Tests Available at NPL
Test Code | Test | Clinical Relevance |
OS364 | MINIMAL RESIDUAL DISEASE (MRD) ANALYSIS FOR T-ALL | Detects residual abnormal cells based on their immunophenotypic (surface marker) profile, tracked against the original diagnostic profile. |
OS417 | MINIMAL RESIDUAL DISEASE (MRD) ANALYSIS FOR B- ALL | Detects residual disease at high sensitivity using specific genetic markers unique to the patient's original malignancy. |
OS533 | MEASURABLE RESIDUAL DISEASE MONITORING FOR ACUTE MYELOID LEUKEMIA (AML MRD) |
|
OS756 | BCR-ABL QUANTITATIVE, MRD MONITOR |
|
OS799 | MINIMAL RESIDUAL DISEASE (MRD) MONITORING FOR MULTIPLE MYELOMA |
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Most tumor molecular tests, histopathology, IHC, and genetic tests do not require fasting. However, some blood-based investigations ordered alongside cancer testing may have specific preparation requirements. Please follow the instructions provided by your doctor or NPL.
Home Sample Collection
MRD testing from peripheral blood can, for some hematological malignancies, be arranged through NPL's standard home sample collection service — confirm with your treating hematologist whether blood-based MRD monitoring applies to your specific disease.
For diseases where MRD assessment requires a bone marrow sample, this must be obtained by a hematologist at a hospital or clinic — this is not a home collection service.
Once your sample (blood or marrow) is obtained, NPL processes MRD testing at our accredited laboratory using the technique appropriate to your original diagnostic markers.
Reports are delivered securely to your treating hematologist, and to you, within the timeframe specified for the test ordered.
When to See a Doctor
• MRD monitoring is scheduled by your treating hematologist as part of your treatment protocol — attend all scheduled monitoring visits
• Contact your hematologist promptly if you develop new symptoms suggestive of disease relapse between scheduled monitoring visits
Medical Disclaimer MRD testing supports treatment monitoring but must be interpreted by a qualified hematologist within the context of the original diagnosis, treatment protocol, and overall clinical picture. This content is for general information only and is not a substitute for medical advice, diagnosis, or treatment. |
