The OncoLife - Myeloma Panel is an advanced genomic profiling test designed to identify clinically significant genetic alterations associated with multiple myeloma. Using next-generation sequencing (NGS), the panel helps oncologists make informed decisions regarding diagnosis, prognosis, targeted therapy selection, and disease monitoring.
Why is this test done?
Supports accurate molecular characterization of multiple myeloma
Identifies actionable genetic mutations linked to targeted therapies
Assists in risk stratification and prognosis
Helps guide personalized treatment decisions
Can support disease monitoring and therapy planning
Who should consider this test?
Patients newly diagnosed with multiple myeloma
Individuals with relapsed or refractory myeloma
Patients being evaluated for targeted or precision oncology treatments
Cases requiring comprehensive genomic assessment
Sample Required
Bone marrow aspirate or other clinically appropriate specimen (as advised by the treating oncologist).