Summary & Overview
CPT 81341: T‑cell Receptor Beta (TCRB) Clonality Analysis, Direct Probe
CPT code 81341 represents a specialized molecular diagnostic laboratory procedure that detects abnormal clonal T‑cell populations by analyzing the T‑cell antigen receptor beta (TCRB/TRB@) using direct probe methods such as Southern blot. This test is clinically important because detection of T‑cell clonality can support the diagnosis and classification of certain leukemias and lymphomas, informing prognosis and downstream diagnostic pathways.
Key payers in the national coverage landscape include Aetna, Blue Cross Blue Shield, Cigna Health, UnitedHealthcare, and Medicare. Readers will find an overview of clinical context for use of this assay, common sites of service (clinical and reference laboratories), and a summary of billing and coding considerations relevant to laboratory and pathology departments. The publication also outlines available benchmarks for utilization and reimbursement patterns where available, highlights policy updates affecting molecular and pathology testing, and explains how this code fits within molecular diagnostic service lines.
This summary is written for a national audience and focuses on clinical relevance, payer coverage contours, and the operational implications for laboratory services. Data not available in the input: associated taxonomies, ICD‑10 diagnoses, related codes, and specific utilization benchmarks.
Billing Code Overview
CPT code 81341 describes a laboratory test that detects abnormal clonal T‑cell populations by analyzing the T‑cell antigen receptor, beta (TCRB or TRB@) using direct probe methods such as Southern blot. The service is a molecular pathology / specialized diagnostic laboratory procedure performed by a lab analyst or molecular technologist to identify clonal T‑cell populations that may indicate certain leukemias or lymphomas.
Service Type: Specialized molecular diagnostic laboratory test (direct probe T‑cell receptor analysis)
Typical Site of Service: Clinical laboratory or reference molecular pathology laboratory
Clinical & Coding Specifications
Clinical Context
A 62-year-old patient with persistent lymphadenopathy, unexplained cytopenias, and B symptoms (fever, night sweats, weight loss) is referred by hematology-oncology for molecular clonality testing to evaluate suspected T-cell lymphoma. Peripheral blood and/or lymph node tissue is submitted to the molecular diagnostics laboratory. The laboratory technologist performs DNA extraction and applies 81341 testing using direct probe methods (for example, Southern blot) to detect abnormal clonal T‑cell populations involving the T‑cell receptor beta locus (TCRB/TRB@). The laboratory issues a report describing presence or absence of clonal rearrangements, which contributes to diagnostic classification, staging, and treatment planning. Typical site of service is an independent or hospital-based clinical molecular pathology laboratory or reference lab. The service type is molecular pathology / targeted clonality testing. The clinical workflow includes specimen accessioning, nucleic acid extraction, probe hybridization (Southern blot or equivalent direct probe method), autoradiography or chemiluminescent detection, result interpretation by a molecular pathologist, and final reporting to the ordering hematologist/oncologist.
Coding Specifications
| Modifier | Description | When to Use |
|---|---|---|
26 | Professional component | Use when billing only the professional interpretation and report by the pathologist or molecular physician. |
TC | Technical component | Use when billing only the technical component (laboratory processing and testing) performed by the facility or reference lab. |
90 | Reference (outside) laboratory | Use when the service was performed by an outside laboratory and billed by the ordering provider as paid to another lab. |
59 | Distinct procedural service | Data not available in the input. |
77 | Repeat procedure by another physician | Data not available in the input. |
52 | Reduced services | Use when the service is partially reduced or limited compared with full 81341 testing. |
53 | Discontinued procedure | Use if testing was started but discontinued due to technical failure or insufficient specimen. |
QX | Ordering/performing laboratory correct coding modifier | Use when the ordering/performing laboratory relationship is reported under applicable CLIA rules (when applicable vendor-specific modifiers are required). |
QY | Ordering/servicing laboratory link | Use where an ordering/servicing laboratory relationship is documented under local coverage rules. |
90 | Duplicate of above; reference lab maintained | Data not available in the input. |
| Taxonomy Code | Specialty | Notes |
|---|---|---|
| 207RH0000X | Hematopathology | Hematopathologists interpret clonality testing and integrate results with morphologic and flow cytometry data. |
| 2080P0227X | Molecular Genetic Pathology | Laboratories specializing in molecular diagnostic testing for hematologic malignancies. |
| 2085R0201X | Clinical Laboratory | Technical laboratories performing molecular assays and Southern blot techniques. |
| 207K00000X | Anatomic and Clinical Pathology | Pathologists responsible for ordering and interpreting specialized clonality studies. |
Related Diagnoses
| ICD-10 Code | Description | Clinical Relevance |
|---|---|---|
C84.0 | Mycosis fungoides | T‑cell clonality testing supports diagnosis when cutaneous T‑cell lymphoma is suspected. |
C84.4 | Peripheral T‑cell lymphoma, unspecified | Molecular evidence of clonal T‑cell receptor rearrangement aids in confirming peripheral T‑cell lymphoma. |
C91.0 | Acute lymphoblastic leukemia, T‑cell type | Clonality testing can identify T‑cell lineage and support diagnosis and minimal residual disease assessment. |
C83.3 | Diffuse large B‑cell lymphoma, immunoblastic type | Included when evaluating differential diagnoses; T‑cell clonality testing helps exclude T‑cell origin. |
R59.0 | Localized enlarged lymph nodes | Indication for biopsy and subsequent clonality testing when malignant etiology is suspected. |
Related CPT Codes
| CPT Code | Description | Relationship to This Procedure |
|---|---|---|
81275 | Immunoglobulin heavy chain (IGH) gene rearrangement analysis; for clonality assessment | Performed alongside T‑cell receptor tests to evaluate B‑cell clonality when differential includes B‑cell lymphoma. |
81445 | Oncology (hematologic/somatic) gene analysis by NGS, larger panels | May be ordered subsequently for broader mutational profiling if clonality testing supports malignancy. |
88312 | Special stains (e.g., immunohistochemistry) | Used on tissue biopsy specimens to correlate molecular clonality with immunophenotype. |
86336 | Immunoassay for tumor markers (e.g., flow cytometry panels reported separately) | Flow cytometry is commonly performed before or alongside molecular clonality testing to define immunophenotype. |
81273 | T-cell receptor gamma (TCRG) gene rearrangement analysis | Frequently ordered with 81341 to increase sensitivity for detecting clonal T‑cell populations. |