
Multiple myeloma is diagnosed through a combination of medical history, blood tests, imaging, and bone marrow biopsy.
- Blood and Urine Tests: samples are checked to measure the amounts of certain antibodies (immunoglobulins)
- Complete Blood Count (CBC)
- Blood Chemistry Tests
- Urine Tests
- Serum Protein Electrophoresis
- Serum Free Light Chain Assays
- Imaging: Determine the size and location of cancer in your bones and other tissues
- CT (Computerized Tomography) Scan
- MRI (Magnetic Resonance Imaging) Scan
- PET (Positron Emission Tomography) Scan
- X-Ray
- Bone Marrow Biopsy: A procedure that involves collecting a small sample of bone marrow, usually from the hip bone, in order to be examined by a laboratory. Tissue included may be used for additional testing such as:
- Cytogenetics: Identifies changes in chromosomes, which can aid in diagnosis. Cytogenetics can also be used to determine treatment plans and the effectiveness of disease therapy.
- Flow Cytometry: Approach for discriminating between normal and clonal plasma cells in multiple myeloma.
- Fluorescence in Situ Hybridization (FISH) Test: A chromosome test used to identify specific genes or chromosome changes.
Related Links
Understanding Myeloma Testing and Monitoring | An Overview
What Should Patients Know About Myeloma Testing?
Questions to Ask Your Doctor About Essential Myeloma Testing
The stage of multiple myeloma is based on:
- Levels of beta-2 microglobulin and albumin in the blood
- Presence of high-risk genetic mutations
- LDH (lactate dehydrogenase) levels
Multiple Myeloma Stages
- Stage I: Low levels of beta-2 microglobulin, normal albumin, and no high-risk genetic markers
- Stage II: Intermediate levels of biomarkers and genetics
Stage III: High beta-2 microglobulin, high-risk cytogenetics, or high LDH
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