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Test Directory

FISH, MET Amplification

Test Summary

The proto-oncogene MET (c-MET) product is the hepatocyte growth factor receptor and encodes tyrosine-kinase activity. Overexpression of MET has been observed in variety of neoplasms such as kidney, lung, head and neck, ovary, breast, thyroid, brain, stomach, pancreas and colon. MET gene amplification, detected by FISH, has been associated with an unfavorable prognosis in non-small cell lung cancer (NSCLC) and resistance to EGFR inhibitors.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

Formalin-fixed, paraffin-embedded tissue block

Minimum Volume

N/A

Instructions

For MET determination in solid tumors, only biopsies with histologically proven tumor involvement should be tested.
Samples that can be tested include tumor biopsy in tissue culture media, formalin fixed paraffin-embedded block or a minimum of 4 charged/ (+)slides from formalin fixed paraffin embedded tissue. Specimen MUST be fixed in 10% neutral buffered formalin. Fixation between 6 and 48 hours is recommended.

Pathology report must accompany paraffin block or slides.

Specimen viability decreases in transit. Send specimen to testing lab for viability determination. Do not reject.

Note: 100 interphase cells are microscopically scored for the copy number of MET and centromere 7 to detect amplification.
If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: See instructions
  • Refrigerated: See instructions
  • Frozen: See instructions

Limitations

N/A

Other Acceptable Specimens

5 x5mm tumor tissue collected in culture transport medium, or 5 micron (4 micron minimum) sections collected on each of (x5) charged slides

Unacceptable Specimens

N/A

Order Code

METFSH

EPIC (Premier) Code

LAB5315

Includes

N/A

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 671080
  • 671081

CPT Statement

Methodology

Fluorescence In Situ Hybridization (FISH)

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
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 - 7 days

Specimen Collection

Special Instructions

N/A

Preferred Specimen

Formalin-fixed, paraffin-embedded tissue block

Minimum Volume

N/A

Instructions

For MET determination in solid tumors, only biopsies with histologically proven tumor involvement should be tested.
Samples that can be tested include tumor biopsy in tissue culture media, formalin fixed paraffin-embedded block or a minimum of 4 charged/ (+)slides from formalin fixed paraffin embedded tissue. Specimen MUST be fixed in 10% neutral buffered formalin. Fixation between 6 and 48 hours is recommended.

Pathology report must accompany paraffin block or slides.

Specimen viability decreases in transit. Send specimen to testing lab for viability determination. Do not reject.

Note: 100 interphase cells are microscopically scored for the copy number of MET and centromere 7 to detect amplification.
If results are not possible, the test order may be canceled and replaced with a Cytogenetics Communication.

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: See instructions
  • Refrigerated: See instructions
  • Frozen: See instructions

Limitations

N/A

Other Acceptable Specimens

5 x5mm tumor tissue collected in culture transport medium, or 5 micron (4 micron minimum) sections collected on each of (x5) charged slides

Unacceptable Specimens

N/A

Billing

CPT Code

  • 88271 (x2)
  • 88275

Billing Code

  • 671080
  • 671081

CPT Statement

Result Information

Methodology

Fluorescence In Situ Hybridization (FISH)

Testing Laboratory

N/A

Reference Range

See Laboratory Report

Setup Schedule / Expected Turnaround Time

Daily; Report available: 5 - 7 days