Summary & Overview
CPT 81419: Genomic Sequence Analysis Panel for Solid Organ Neoplasms
CPT code 81419 represents a genomic sequence analysis panel for solid organ neoplasms, focusing on DNA analysis of 5 to 50 genes. This advanced laboratory service is pivotal in cancer diagnostics, offering detailed genetic insights that inform treatment strategies and support precision medicine. The code is widely recognized across major national payers, including Aetna, Blue Cross Blue Shield, Cigna Health, and UnitedHealthcare, reflecting its importance in clinical and reimbursement settings.
This publication provides a comprehensive overview of 81419, covering payer coverage, clinical context, and relevant policy updates. Readers will gain insight into benchmarks for utilization, the role of independent laboratories, and the significance of this code in the evolving landscape of molecular pathology. The analysis also highlights associated modifiers, taxonomies, and related CPT codes, offering a clear understanding of how 81419 fits within broader oncology testing protocols. The summary is designed for healthcare professionals, administrators, and policy stakeholders seeking up-to-date information on genomic testing for solid organ cancers.
CPT Code Overview
CPT code 81419 is used for genomic sequence analysis panels targeting solid organ neoplasms. This procedure involves DNA analysis of 5 to 50 genes, providing critical information for the diagnosis and management of various cancers. The service falls under Pathology and Laboratory, with the typical site of service being an Independent Laboratory (Place of Service 81). This code enables comprehensive genetic profiling, supporting precision medicine approaches in oncology.
Clinical & Coding Specifications
Clinical Context
A patient diagnosed with a solid organ malignancy, such as lung, breast, colon, prostate, or pancreatic cancer, is referred for advanced molecular testing. The treating physician requests a genomic sequence analysis panel to identify DNA mutations across 5-50 genes relevant to the neoplasm. The specimen, typically a tissue biopsy from the affected organ, is sent to an independent laboratory (Place of Service 81) specializing in molecular pathology. The laboratory performs the analysis using CPT code 81419, generating a report that assists the oncology team in determining targeted therapies or prognostic information. The workflow involves specimen collection, laboratory processing, genomic sequencing, and interpretation by a pathologist or molecular genetic specialist.
Coding Specifications
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Modifiers:
- Modifier
26: Used to indicate the professional component, when only the interpretation of the test is performed by the provider. - Modifier
59: Used to denote a distinct procedural service, when the procedure is separate from other services performed on the same day.
- Modifier
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Provider Taxonomies:
Code Specialty Name 207ZP0102XPathology - Clinical Pathology/Laboratory Medicine 207ZP0007XPathology - Molecular Genetic Pathology 207Q00000XFamily Medicine Physician
These taxonomies represent providers qualified to order, interpret, or perform genomic sequence analysis panels.
Related Diagnoses
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C34.90: Malignant neoplasm of unspecified part of unspecified bronchus or lung- Relevant for patients with lung cancer undergoing genomic analysis to guide therapy.
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C50.919: Malignant neoplasm of unspecified site of unspecified female breast- Used for breast cancer cases where molecular profiling informs treatment decisions.
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C18.9: Malignant neoplasm of colon, unspecified- Applicable for colon cancer patients, as genomic panels help identify actionable mutations.
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C61: Malignant neoplasm of prostate- For prostate cancer, genomic sequencing may reveal mutations affecting prognosis or therapy.
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C25.9: Malignant neoplasm of pancreas, unspecified- Pancreatic cancer patients benefit from genomic analysis to determine targeted treatment options.
Each diagnosis code represents a solid organ neoplasm for which CPT code 81419 is clinically indicated.
Related CPT Codes
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81445: Targeted genomic sequence analysis panel, solid organ neoplasm, DNA analysis, 5-50 genes- Closely related to
81419, often used as an alternative depending on panel specifics.
- Closely related to
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88342: Immunohistochemistry, per specimen; initial single antibody stain procedure- Used to assess protein expression in tumor tissue, commonly performed alongside genomic sequencing.
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88341: Immunohistochemistry, per specimen; each additional single antibody stain procedure- Used for additional antibody stains, often in conjunction with
88342and genomic analysis.
- Used for additional antibody stains, often in conjunction with
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81210: BRAF gene analysis, V600E variant- Specific gene analysis that may be included in the panel for certain neoplasms, sometimes ordered separately if not covered by the panel.
These codes are frequently used together in comprehensive cancer diagnostics or as alternatives based on clinical needs.
National Reimbursement Benchmarks
For CPT code 81419, national mean rates among commercial payers (BUCA average) are $1,962.02, which are substantially higher than typical Medicare rates, though Medicare data is not available in the input for comparison. Among individual commercial payers, Cigna has the highest mean rate at $2,117.23, while Aetna is the lowest at $1,863.85.
Rate dispersion, measured by the difference between the 75th and 25th percentiles, varies significantly across payers. Blue Cross Blue Shield (BCBS) shows the widest spread at $1,060.60, indicating greater variability in contracted rates. In contrast, Aetna has the tightest range at $725.75, suggesting more consistent reimbursement levels. Cigna also exhibits a wide range of $1,686.50, reflecting substantial rate variability.
The table and chart below present a detailed breakdown of national mean rates and percentile distributions for each payer.
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