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NEXTGEN ALL RISK STRATIFICATION GENE PANEL BY NGS B ALL, EDTA BLOOD

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 NABL Cap Accredited 
The NextGen ALL Risk Stratification Gene Panel for B-ALL at Metropolis Healthcare provides a comprehensive genomic evaluation to identify key mutations that influence prognosis and treatment outcomes in B-cell Acute Lymphoblastic Leukemia. This advanced NGS-based test helps clinicians categorize patients into appropriate risk groups, ensuring more personalized and effective therapy planning. Metropolis Healthcare uses high-resolution sequencing to detect clinically significant variants associated with relapse risk, drug resistance, and targeted therapy eligibility. This panel is especially valuable for newly diagnosed, relapsed, or treatment-refractory B-ALL cases.

  • 17 Crores+ Samples Processed
  • World Class Technology Labs
  • 25+ Years of Trust & Experience
  • Free Home Collection

Price: Rs. 21,000.00

Sample Type: EDTA Blood

Fasting Not Required


Notes:N8277

Frequently Asked Questions (FAQ's):

 What does the NextGen B-ALL Risk Stratification Panel include?

It assesses multiple leukemia-associated genes to detect mutations that impact prognosis, treatment response, and disease aggressiveness.

Why is this test important?
It helps determine patient-specific risk levels, enabling oncologists to choose optimal treatment intensity and targeted therapies.

Who should take this test?
Patients diagnosed with B-cell Acute Lymphoblastic Leukemia who are beginning treatment, undergoing reassessment, or experiencing relapse may need this panel.

How does Metropolis Healthcare perform this test?
Metropolis Healthcare utilizes high-depth Next Generation Sequencing to identify single nucleotide variants, indels, and other relevant mutations.

What sample is required?
A blood sample collected in an EDTA vial is needed for genetic analysis.

Is any special preparation required?
No special preparation or fasting is needed before sample collection.

How fast are the results available?
Metropolis Healthcare provides a detailed genomic report within a clinically appropriate timeframe to guide timely decisions.

Can this test guide treatment strategies?
Yes, the results help tailor chemotherapy, immunotherapy, and targeted therapy approaches based on individual genetic risk factors

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