Measurable Residual Disease (MRD) Assessment Testing 2.02.54
Summary
Excellus policy 2.02.54 considers the ClonoSEQ Assay medically appropriate for measurable residual disease assessment only for acute lymphoblastic leukemia, chronic lymphocytic leukemia and multiple myeloma, the FDA approved indications. Flow cytometry is considered medically necessary to detect MRD in patients with leukemia, lymphoma or multiple myeloma, and MRD assessment is considered investigational for all other indications when using tests including Signatera, MyMRD, Guardant Reveal, Northstar Response, Invitae PCM MRD Monitoring, PCM Tissue Profiling and MRD Monitoring, HPV-SEQ and UroAmp MRD. The 08/20/26 annual review removed codes 0450U and 0451U and states that policy intent is unchanged.
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