Banner Image

Test Directory

T-Cell Clonality Panel (TCRB, TCRG), PCR

Test Summary

This test, which interrogates both the T-cell receptor beta (TCRB) locus and the T-cell receptor gamma (TCRG) locus by a PCR method based on the BIOMED-2 consensus, is useful in patients with suspected T-cell malignancies or to evaluate for residual disease after treatment. Several published studies have demonstrated that the combination of TCRB and TCRG PCR using the BIOMED-2 method can detect virtually all clonal T-cell populations.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

5 mL whole blood or 3 mL bone marrow aspirate collected in an EDTA (lavender-top) tube • 8 unstained positively charged slides

Minimum Volume

3 mL whole blood • 1 mL bone marrow aspirate • 4 slides • 1 block

Instructions

Do not reject specimens, send to laboratory for screening.

8 unstained sections on glass slides labeled with surgical case number (pathology report required, indicate if fixative is not formalin) Please include pathology report for frozen tissue and FFPE cases (partial/preliminary reports acceptable).

Needle washings (acceptable): in alcohol based fixative (eg. CytoLyt) are acceptable.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Fresh tissue: Frozen
All other specimens: Room temperature

Specimen Stability

  • Whole blood and bone marrow aspirate
  • Room temperature: 7 days
  • Refrigerated: 7 days
  • Frozen: Unacceptable
  • FFPE/Slides
  • Room temperature: 5 years
  • Refrigerated: 5 years
  • Fro

Limitations

N/A

Other Acceptable Specimens

Whole blood or bone marrow aspirate collected in a sodium heparin (green-top) tube • Formalin-fixed, paraffin-embedded tissue • Fresh Tissue

Unacceptable Specimens

N/A

Order Code

TCCP

EPIC (Premier) Code

LAB5397

Includes

Pathologist Interpretation

CPT Code

  • 81340
  • 81342
  • 84999 (HCPCS: G0452)

Billing Code

  • 670802
  • 670803
  • 670804

CPT Statement

Methodology

Polymerase Chain Reaction (PCR) • Fragment Analysis

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
33608 Ortega Highway
San Juan Capistrano CA, 92675

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

5 mL whole blood or 3 mL bone marrow aspirate collected in an EDTA (lavender-top) tube • 8 unstained positively charged slides

Minimum Volume

3 mL whole blood • 1 mL bone marrow aspirate • 4 slides • 1 block

Instructions

Do not reject specimens, send to laboratory for screening.

8 unstained sections on glass slides labeled with surgical case number (pathology report required, indicate if fixative is not formalin) Please include pathology report for frozen tissue and FFPE cases (partial/preliminary reports acceptable).

Needle washings (acceptable): in alcohol based fixative (eg. CytoLyt) are acceptable.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Fresh tissue: Frozen
All other specimens: Room temperature

Specimen Stability

  • Whole blood and bone marrow aspirate
  • Room temperature: 7 days
  • Refrigerated: 7 days
  • Frozen: Unacceptable
  • FFPE/Slides
  • Room temperature: 5 years
  • Refrigerated: 5 years
  • Fro

Limitations

N/A

Other Acceptable Specimens

Whole blood or bone marrow aspirate collected in a sodium heparin (green-top) tube • Formalin-fixed, paraffin-embedded tissue • Fresh Tissue

Unacceptable Specimens

N/A

Billing

CPT Code

  • 81340
  • 81342
  • 84999 (HCPCS: G0452)

Billing Code

  • 670802
  • 670803
  • 670804

CPT Statement

Result Information

Methodology

Polymerase Chain Reaction (PCR) • Fragment Analysis

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 days