Aetna modified CPB 0871 covering hematopoietic cell transplantation (HCT) for inherited metabolic disorders and genetic diseases, effective January 5, 2026. Here's what billing teams need to know.
Aetna, a CVS Health company, updated this coverage policy to clarify which conditions qualify for allogeneic HCT and which procedures remain experimental or non-covered. The policy governs CPT codes 38204 through 38243 and HCPCS codes S2142 and S2150. If your team bills transplant preparation, harvesting, or infusion codes for diagnoses like Hurler's syndrome (E76.1), Krabbe disease (E75.23), or metachromatic leukodystrophy (E75.25), this update affects your claims.
Quick-Reference Table
| Field | Detail |
|---|---|
| Payer | Aetna, a CVS Health company |
| Policy | Hematopoietic Cell Transplantation for Inherited Metabolic Disorders and Genetic Diseases |
| Policy Code | CPB 0871 Aetna |
| Change Type | Modified |
| Effective Date | January 5, 2026 |
| Impact Level | High — transplant programs and pediatric specialty centers |
| Specialties Affected | Hematology/oncology, pediatric subspecialties, transplant programs, metabolic disease centers |
| Key Action | Audit active prior authorization requests and charge capture for allogeneic vs. autologous transplant codes before billing against this policy |
Aetna HCT Coverage Criteria and Medical Necessity Requirements 2026
The Aetna HCT coverage policy under CPB 0871 draws a hard line between allogeneic and autologous transplant. Allogeneic HCT is covered for a defined list of inherited metabolic disorders. Autologous HCT is not covered for any of the indications in this policy. That distinction drives most of the claim denial risk here.
To meet medical necessity under CPB 0871, allogeneic HCT must be used for one of these confirmed diagnoses:
| # | Covered Indication |
|---|---|
| 1 | Alpha-mannosidosis (E77.1) |
| 2 | Childhood-onset adrenoleukodystrophy (E71.511) |
| 3 | Erythropoietic protoporphyria with severe hepatopathy (E80.0) |
| 4 | Fucosidosis (E77.1) |
| 5 | Globoid cell leukodystrophy — Krabbe disease (E75.23) |
| 6 | Metachromatic leukodystrophy (E75.25) |
| 7 | Mucolipidoses (E77.0, E77.1) |
| 8 | Mucopolysaccharidosis — including Hunter's, Hurler's, Sanfilippo's, Maroteaux-Lamy, Morquio, and Sly syndromes (E76.1, E76.2, E76.3, E76.8, E76.9) |
| 9 | Wolman disease (E75.5) |
Each of these has specific ICD-10-CM codes. Map them correctly. Billing 38240 (allogeneic HPC transplantation per donor) against the wrong diagnosis code will trigger a denial even when the clinical case is solid.
Fanconi anemia has its own criteria. Allogeneic HCT is medically necessary for children and adolescents with Fanconi anemia who meet any one of the following: they have failed supportive care, androgens, and hematopoietic growth factors; they cannot tolerate those approaches; or they have developed severe bone marrow failure, myelodysplasia, or acute myeloid leukemia. Documentation of any one of these pathways is sufficient — you don't need all three.
Infantile malignant osteopetrosis also has specific criteria. Allogeneic HCT is covered when the diagnosis is confirmed by both bone biopsy and radiographic imaging, and when the patient does not show irreversible neurologic impairment or multi-organ failure. Miss either of those documentation elements and you're exposed on prior auth.
CPB 0871 does not state specific prior authorization requirements. Contact Aetna directly to confirm PA requirements for your specific plan and member contract.
Aetna HCT Exclusions and Non-Covered Indications
Aetna's experimental and non-covered list under this coverage policy is worth reading carefully. These are the claims most likely to get denied — and some of the diagnoses may look clinically similar to covered ones.
Barakat syndrome (HDR syndrome): Aetna classifies allogeneic HCT for this condition as experimental. The source policy does not address autologous HCT for Barakat syndrome separately.
Autologous HCT: Codes 38206 (autologous blood-derived harvesting), 38232 (autologous bone marrow harvesting), and 38241 (autologous HPC transplantation) are not covered for any indication listed in CPB 0871. If you're billing autologous transplant codes for mucopolysaccharidosis or childhood-onset adrenoleukodystrophy, expect a denial.
HCT — autologous, allogeneic, or cord blood — for these conditions is experimental:
| # | Excluded Procedure |
|---|---|
| 1 | Hereditary corneal defects (see full policy for complete ICD-10 code list) |
| 2 | Huntington's disease (G10) |
| 3 | TRNT1 enzyme deficiency (E88.09) |
The Huntington's disease exclusion catches people off guard. The ICD-10 code G10 shows up in this policy's code set, but it's listed as a non-covered indication. If a patient has G10 and a team requests HCT, the claim dies on arrival under this policy.
The TRNT1 exclusion is newer and worth flagging. This is a rare mitochondrial disorder, and some centers have been exploring HCT as a treatment. Aetna is not covering it under CPB 0871.
Coverage Indications at a Glance
| Indication | Status | Relevant ICD-10 | Notes |
|---|---|---|---|
| Alpha-mannosidosis | Covered (allogeneic only) | E77.1 | Confirm PA requirements with Aetna |
| Childhood-onset adrenoleukodystrophy | Covered (allogeneic only) | E71.511 | Confirm PA requirements with Aetna |
| Fanconi anemia | Covered (allogeneic only) | D61.09 | Document any one of: failure of or inability to tolerate supportive care/androgens/growth factors; OR severe BM failure/MDS/AML |
| Erythropoietic protoporphyria with severe hepatopathy | Covered (allogeneic only) | E80.0 | "Severe hepatopathy" must be documented |
| Fucosidosis | Covered (allogeneic only) | E77.1 | Confirm PA requirements with Aetna |
| Krabbe disease (Globoid cell leukodystrophy) | Covered (allogeneic only) | E75.23 | Confirm PA requirements with Aetna |
| Metachromatic leukodystrophy | Covered (allogeneic only) | E75.25 | Confirm PA requirements with Aetna |
| Mucolipidoses | Covered (allogeneic only) | E77.0, E77.1 | Confirm PA requirements with Aetna |
| Mucopolysaccharidosis (all subtypes) | Covered (allogeneic only) | E76.1, E76.2, E76.3, E76.8, E76.9 | Includes Hunter's, Hurler's, Sanfilippo's, Maroteaux-Lamy, Morquio, Sly syndromes |
| Wolman disease | Covered (allogeneic only) | E75.5 | Confirm PA requirements with Aetna |
| Infantile malignant osteopetrosis | Covered (allogeneic only) | — | Requires bone biopsy + radiographic confirmation; no irreversible neuro impairment or multi-organ failure |
| Barakat syndrome (HDR syndrome) | Experimental — Not Covered | — | Allogeneic HCT classified as experimental; policy does not address autologous separately |
| Infantile malignant osteopetrosis (autologous) | Not Covered | — | Autologous HCT only |
| Mucopolysaccharidosis (autologous) | Not Covered | — | Autologous HCT only |
| Childhood-onset adrenoleukodystrophy (autologous) | Not Covered | — | Autologous HCT only |
| Hereditary corneal defects | Experimental — Not Covered | See full policy for complete code list | All HCT types excluded |
| Huntington's disease | Experimental — Not Covered | G10 | All HCT types excluded |
| TRNT1 enzyme deficiency | Experimental — Not Covered | E88.09 | All HCT types excluded |
Aetna HCT Billing Guidelines and Action Items 2026
The effective date for this updated policy is January 5, 2026. Review open claims and active prior authorizations before submitting new requests.
| # | Action Item |
|---|---|
| 1 | Audit every pending HCT prior auth for allogeneic vs. autologous designation. Autologous codes 38206, 38232, and 38241 are not covered under CPB 0871 for any indication. If any open auth was submitted with these codes for diagnoses in this policy, pull it and resubmit or redirect. |
| 2 | Lock down your Fanconi anemia documentation before billing 38240. Aetna requires evidence of any one of the following: failure of or inability to tolerate supportive care, androgens, and hematopoietic growth factors; or documented bone marrow failure, myelodysplasia, or AML. Any single pathway is sufficient — but it must be in the record before you bill. Missing documentation is a clean denial. |
| 3 | Verify ICD-10 specificity on all MPS claims. Mucopolysaccharidosis maps to E76.1, E76.2, E76.3, E76.8, and E76.9. Unspecified or wrong-subtype coding will flag on edit. Confirm the subtype with your clinical team and use the most specific available code. |
| 4 | Remove G10 (Huntington's disease) from any HCT charge capture templates. It's in the policy's ICD-10 list as a non-covered indication. If a template has it bundled with covered diagnoses, you'll generate phantom authorizations that won't pay. |
| 5 | For osteopetrosis cases, document bone biopsy and radiographic imaging in the prior auth. Aetna's criteria require both. Radiographic imaging alone isn't enough. If the record only shows imaging, the auth will likely fail regardless of the clinical picture. |
| 6 | Confirm cord blood and allogeneic stem cell claims use HCPCS S2142 or S2150. These are covered when selection criteria are met. Make sure your HCPCS capture is active in your billing system for these codes — they're easy to miss in transplant workflows that default to CPT. |
| 7 | Cross-check CPB 0871 with related Aetna policies if your team also handles lysosomal storage disorders. CPB 0442 (Lysosomal Storage Disorders Treatments) and CPB 0626 (HCT for Thalassemia Major and Sickle Cell Anemia) have overlapping diagnosis territory. If you're billing for Gaucher's disease or thalassemia, the coverage determination may be in a different CPB. |
If you treat a high volume of these rare diagnoses and you're not sure how this policy intersects with your payer mix, loop in your compliance officer before the January 5, 2026 effective date passes without a review.
| Previous Version | Current Version |
|---|---|
| Coverage is considered experimental and investigational for all indications | Coverage is considered medically necessary when specific criteria are met |
| Prior authorization is not required | Prior authorization is required for initial treatment |
| Documentation must include clinical history | Documentation must include clinical history |
| Re-review every 24 months | Re-review every 12 months with updated clinical documentation |
CPT, HCPCS, and ICD-10 Codes for HCT Under CPB 0871
Covered CPT Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| 38204 | CPT | Management of recipient hematopoietic progenitor cell donor search and cell acquisition |
| 38205 | CPT | Blood-derived hematopoietic progenitor cell harvesting for transplantation, per collection; allogeneic |
| 38207 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38208 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38209 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38210 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38211 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38212 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38213 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38214 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38215 | CPT | Transplant preparation of hematopoietic progenitor cells |
| 38230 | CPT | Bone marrow harvesting for transplantation; allogeneic |
| 38240 | CPT | Hematopoietic progenitor cell (HPC); allogeneic transplantation per donor |
| 38242 | CPT | Allogeneic lymphocyte infusions |
| 38243 | CPT | Hematopoietic progenitor cell (HPC); HPC boost |
| S2142 | HCPCS | Cord blood-derived stem-cell transplantation, allogeneic |
| S2150 | HCPCS | Bone marrow or blood-derived stem cells (peripheral or umbilical), allogeneic or autologous, harvest |
Not Covered / Experimental Codes
| Code | Type | Description | Reason |
|---|---|---|---|
| 38206 | CPT | Blood-derived hematopoietic progenitor cell harvesting for transplantation, per collection; autologous | Not covered for indications listed in CPB 0871 |
| 38232 | CPT | Bone marrow harvesting for transplantation; autologous | Not covered for indications listed in CPB 0871 |
| 38241 | CPT | Hematopoietic progenitor cell (HPC); autologous transplantation | Not covered for indications listed in CPB 0871 |
Key ICD-10-CM Diagnosis Codes
| Code | Description | Coverage Status |
|---|---|---|
| D61.09 | Other constitutional aplastic anemia | Covered (Fanconi anemia pathway) |
| E71.511 | Neonatal adrenoleukodystrophy (childhood-onset adrenoleukodystrophy) | Covered |
| E75.23 | Krabbe disease | Covered |
| E75.25 | Metachromatic leukodystrophy | Covered |
| E75.5 | Other lipid storage disorders (Wolman's disease) | Covered |
| E76.1 | Disorders of glycosaminoglycan metabolism (Mucopolysaccharidosis) | Covered |
| E76.2 | Disorders of glycosaminoglycan metabolism (Mucopolysaccharidosis) | Covered |
| E76.3 | Disorders of glycosaminoglycan metabolism (Mucopolysaccharidosis) | Covered |
| E76.8 | Disorders of glycosaminoglycan metabolism (Mucopolysaccharidosis) | Covered |
| E76.9 | Disorders of glycosaminoglycan metabolism (Mucopolysaccharidosis) | Covered |
| E77.0 | Defects in post-translational modification of lysosomal enzymes (Mucolipidosis II, Mucolipidosis III) | Covered |
| E77.1 | Defects in glycoprotein degradation (Alpha-mannosidosis, Fucosidosis, Mucolipidosis I) | Covered |
| E80.0 | Hereditary erythropoietic porphyria | Covered (with severe hepatopathy) |
| E88.09 | Other disorders of plasma-protein metabolism (TRNT1 enzyme deficiency) | Experimental — Not Covered |
| G10 | Huntington's disease | Experimental — Not Covered |
| H18.501–H18.539+ | Hereditary corneal dystrophies | Experimental — Not Covered — See full policy for complete code list; source includes additional codes beyond H18.539 |
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