Multiple Myeloma Test

What is Multiple Myeloma?

Multiple Myeloma is the cancer of plasma cells, a type of white blood cell found in the bone marrow that produces antibodies. In multiple myeloma, abnormal plasma cells multiply uncontrollably and produce an excess monoclonal protein (M protein), leading to complications such as bone damage, anaemia, kidney dysfunction, and immune suppression. It is often preceded by precursor conditions like MGUS or smouldering myeloma. Diagnosis involves a combination of blood and urine tests, bone marrow analysis, and advanced genetic tools such as FISH and NGS for risk stratification and treatment planning.

Disease Staging and Risk Stratification Systems for Multiple Myeloma

StageInternational Staging System (ISS)Revised ISS (R-ISS)
ISerum beta-2 microglobulin < 3.5 mg/L
Serum albumin ≥ 3.5 g/dL.
ISS stage I and standard-risk
chromosomal abnormalities by FISH and
serum LDH ≤ upper limit of normal.
IINot ISS stage I or III.Not ISS stage I or III.
IIISerum beta-2 microglobulin ≥ 5.5 mg/L..ISS stage III and either high-risk
chromosomal abnormalities by FISH or
serum LDH > upper limit of normal.

Diagnostic Criteria of Multiple Myeloma as per NCCN, 2025 Guidelines

  • History and physical examination.
  • CBC, differential, and platelet count.
  • Peripheral blood smear.
  • Serum BUN/creatinine, electrolytes, liver function tests, albumin, calcium, serum uric acid, serum LDH, and beta-2 microglobulin.
  • Creatinine clearance (calculated or measured directly).
  • Serum quantitative immunoglobulins, serum protein electrophoresis (SPEP), and serum immunofixation electrophoresis (SIFE).
  • 24-hour urine for total protein, urine protein electrophoresis (UPEP), and urine immunofixation electrophoresis (UIFE).
  • Serum-free light chain (FLC) assay.
  • Whole-body low-dose CT scan or FDG PET/CT Bone marrow aspirate and biopsy, including immunohistochemistry (IHC) and/or multiparameter flow cytometry.
  • FISH panel on bone marrow for chromosomal abnormalities: del(13), del(17p13), t(4;14), t(11;14), t(14;16), t(14;20), 1q21 gain/1q21 amplification, 1p deletion.
  • Natriuretic Peptide Tests (BNP, NT-proBNP).

Methodologies & Technologies Used

  • SPEP & SIFE: Serum Protein Electrophoresis & Immunofixation.
  • UIFE & UPEP: Urine Electrophoresis & Immunofixation.
  • FLC : Free Light Chain Assay.
  • FC MRD: Flow Cytometric Minimal Residual Disease.
  • FISH Panel: Fluorescence in Situ Hybridization.
  • BMA: Bone Marrow Analysis.
  • NGS Panel : Next-Generation Sequencing.
  • CBC: Complete Blood Count & Biochemistry.

Multiple Myeloma Tests Offered by MedGenome

Key Highlights of MedGenome's Multiple Myeloma Test

Rapid Results for Critical Parameters

Test results are available within 8 hours to 5–7 working days, depending on the type of test.

Advanced MRD Sensitivity

Multiparameter flow cytometry detects residual disease with a sensitivity of 0.005%.

Covers All Plasma Cell Dyscrasias

Suitable for MGUS, smouldering myeloma, symptomatic MM, and non-secretory variants.

What is Multiple Myeloma?

Multiple myeloma is a type of blood cancer that affects plasma cells, the white blood cells found in bone marrow that produce antibodies to fight infections. In multiple myeloma, abnormal plasma cells multiply uncontrollably and produce a single type of protein (M protein), which can damage bones, kidneys, and the immune system. Early detection and regular monitoring are crucial for effective treatment and long-term management.

How Is the Multiple Myeloma Test Done?

StepDescription
1. Blood TestsEvaluates proteins, calcium, LDH, kidney function, and free light chains.
2. Urine Analysis24-hour collection used to detect Bence-Jones proteins (light chains).
3. Bone Marrow AspirationChecks for abnormal plasma cells and helps with immunotyping and FISH studies.
4. Imaging TestsLow-dose CT or PET scans to identify bone damage or lesions.
5. Genetic Testing (FISH/NGS)Detects chromosomal abnormalities and gene mutations linked to multiple myeloma.
Why Do You Need a Multiple Myeloma Test?

A Multiple Myeloma Test is essential for diagnosing, staging, and monitoring this complex condition. It helps detect the presence of abnormal M protein, assess bone marrow involvement, and identify genetic abnormalities that influence prognosis and treatment. Timely testing can guide in choosing the most effective therapy and tracking disease progression or response to treatment.

How Does the Multiple Myeloma Test Work?
Who Should Consider the Multiple Myeloma Test?

You should consider a Multiple Myeloma Test if you have:

  • Persistent bone pain, especially in the back or ribs.
  • Fatigue, weakness, or frequent infections.
  • High calcium levels or kidney dysfunction.
  • A family history of plasma cell disorders.
  • An unexplained rise in protein levels in blood or urine.
  • Symptoms that suggest monoclonal gammopathy, MGUS, or smouldering myeloma.

Testing is also recommended for ongoing monitoring in patients already diagnosed with Multiple Myeloma.

What Do Multiple Myeloma Test Results Mean?
When is the Best Time to Get a Multiple Myeloma Test?

The best time to get a multiple myeloma test is:

  • When you have symptoms or blood work suggesting plasma cell disorders.
  • After a diagnosis of MGUS or smouldering myeloma, monitor the progression.
  • At diagnosis, for risk stratification and treatment planning.
  • After treatment, to assess minimal residual disease (MRD) and prevent relapse.

Clinical correlation and regular testing is recommended.

Why Choose MedGenome for Multiple Myeloma Testing?

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