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FISH, MET Amplification
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Test Code
METFSH
CPT Codes
88271 (x2), 88275
Preferred Specimen
Formalin-fixed, paraffin-embedded tissue block
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
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.
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.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: See instructions
Refrigerated: See instructions
Frozen: See instructions
Refrigerated: See instructions
Frozen: See instructions
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. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Daily; Report available: 5-7 days
Reference Range
See Laboratory Report
Clinical Significance
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.
Performing Laboratory
Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly, VA 20153
Last Updated: November 24, 2021