Single Gene and Molecular Biomarker Testing for Solid Tumors - Medicare Advantage (Revised)
Effective date
Oct 12, 2026
Identified
Oct 15, 2026
Summary
Humana Medicare Advantage revised its policy on Single Gene and Molecular Biomarker Testing for Solid Tumors, effective 10/12/2026. The policy now applies to testing such as FGFR, KIT, KRAS, MET, NRAS, NTRK, PDGFRA, PIK3CA, RET, ROS1, TERT, TP53, PD-L1, FOLR1, and related molecular biomarker tests (including IHC, MGMT promoter methylation, MSI/MMR). Billing teams must verify current coverage determinations and coding requirements under the revised policy and associated MAC LCDs/LCAs referenced for their geographic jurisdiction.
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01Already effective 10/12/2026: Billing team should verify that the practice's current billing workflows, prior authorization processes, and coding submissions for single gene and molecular biomarker testing align with Humana's revised HUM-1236-004 policy.
02Review the specific MAC LCD/LCA documents applicable to your geographic jurisdiction (listed in the Related CMS Documents section by state and contractor) to confirm which tests require prior authorization, which CPT/HCPCS codes are covered, and any documentation requirements.
03Update internal billing guidelines and prior authorization submission templates as needed to reflect coverage determinations in the revised policy.
04Recommend confirming current applicability with Humana directly, as the source document does not specify what substantive coverage changes were made in the revision from the original 05/01/2025 effective date.
Original notice
Single Gene and Molecular Biomarker Testing for Solid Tumors - Medicare Advantage (Revised)
mcp.humana.com · Always check the source before changing claims.
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