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AetnaCommercial · Coverage · Medical Policy · Oncology, HematologyMedium impact

Decitabine (CPB 0868, reviewed 2026-06-10)

Effective date
Not stated in the notice
Identified
Aug 13, 2026

Summary

Aetna considers decitabine medically necessary for accelerated or blast phase myeloproliferative neoplasm, acute myeloid leukemia, blastic plasmacytoid dendritic cell neoplasm when used with venetoclax, classic Hodgkin lymphoma when used with pembrolizumab and refractory to at least three prior lines of therapy, myelodysplastic syndromes, and myelodysplastic syndrome/myeloproliferative neoplasm overlap neoplasms. Continuation of decitabine is considered medically necessary for those indications when there is no evidence of unacceptable toxicity or disease progression on the current regimen. Aetna considers decitabine experimental, investigational, or unproven for all other indications, including colon, lung, melanoma, ovarian and other solid tumors, multiple myeloma, sickle cell disease, and use in combination with azacitidine.

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What to do

Action · 6 steps
01Confirm the diagnosis is one of the covered indications before billing decitabine.
02For BPDCN, confirm decitabine is used with venetoclax.
03For classic Hodgkin lymphoma, confirm decitabine is used with pembrolizumab and the disease is refractory to at least three prior lines of therapy.
04Bill HCPCS J0893, which covers decitabine (sun pharma) not therapeutically equivalent to J0894 per 1 mg, only when the selection criteria are met.
05Do not bill decitabine for the experimental indications listed in this policy, including use in combination with azacitidine, since Aetna considers those experimental, investigational, or unproven.
06For continuation claims, document that there is no evidence of unacceptable toxicity or disease progression on the current regimen.

Codes mentioned

J0893J0894J9271C92.20C94.6D46.AD46.BD46.CD46.ZD47.1G61.0C54.1

Original notice

Decitabine (CPB 0868, reviewed 2026-06-10)
aetna.com · Always check the source before changing claims.
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