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HCPCS Level II · Medical services and quality measures

M1412Patients with metastatic nsclc with epidermal growth factor receptor (egfr) mutations, alk genomic tumor aberrations, or other targetable genomic abnormalities with approved first-line targeted therapy, such as nsclc with ros1 rearrangement, braf v600e mutation, ntrk 1/2/3 gene fusion, met ex14 skipping mutation, and ret rearrangement

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Source: CMS HCPCS quarterly update, October 2026. Page updated September 29, 2026.

About M1412

M1412 is an HCPCS Level II code in the M series (medical services and quality measures), describing patients with metastatic nsclc with epidermal growth factor receptor (egfr) mutations, alk genomic tumor aberrations, or other targetable genomic abnormalities with approved first-line targeted therapy, such as nsclc with ros1 rearrangement, braf v600e mutation, ntrk 1/2/3 gene fusion, met ex14 skipping mutation, and ret rearrangement.

It was added to HCPCS effective 01/01/2025.

Its Medicare coverage code is "C", meaning coverage is left to the Medicare contractor's judgment.

Details

Short description
Met nsclc w/ egfr alk oth ab
Date added
01/01/2025
Action effective
01/01/2025
BETOS
Z2

Related M14xx codes

Common questions about M1412

Is HCPCS M1412 still valid?

Yes. M1412 is active in the CMS October 2026 HCPCS file.

Does Medicare cover M1412?

Its coverage code is "C": coverage is left to the Medicare contractor's judgment. Check the local coverage determination for your region.