MLH1 Methylation

Test Code
39782


CPT Codes
81288

Preferred Specimen
5 mL whole blood collected in an EDTA (lavender-top) tube or ACD (yellow-top) tube or
100 ng extracted DNA from CLIA-certified laboratory collected in TE or sterile water or
Formalin-fixed paraffin-embedded tissue block or
1 H&E slide and 5 (2) unstained, non-baked slides with 5-10 um thick tumor sections


Minimum Volume
Formalin-fixed paraffin-embedded tissue: 1 Block Extracted DNA from CLIA-certified laboratory: 10 ng Whole blood: 3 mL


Other Acceptable Specimens
Whole blood collected in sodium heparin (green-top) tube (not recommended)


Instructions
Whole blood is shipped ambient (18°C to 26°C). Do not freeze whole blood.
Extracted DNA is shipped refrigerated (2°C to 8°C).
Paraffin-embedded tissue is shipped ambient.
Section (slides): Room temperature
Extracted DNA: 100 ng (10 ng) or more in TE or sterile water. Please send Pathology report.


Transport Temperature
Room temperature


Specimen Stability
Whole blood
Room temperature: 8 days
Refrigerated: 8 days
Frozen: Unacceptable

FFPE
Room temperature: 5 years
Refrigerated: 5 years
Frozen: Unacceptable

Extracted DNA
Room temperature: 5 years
Refrigerated: 5 years
Frozen: 10 years

Slides
Room temperature: 5 years
Refrigerated: Unacceptable
Frozen: Unacceptable


Reject Criteria (Eg, hemolysis? Lipemia? Thaw/Other?)
Baked slide


Methodology
Real-Time Polymerase Chain Reaction

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
A.M. Sets up 1 day a week.


Report Available
Reports in 7 to 14 days.


Clinical Significance
The MLH1 methylation assay is designed to target methylated CpG residues in the “C region of the MLH1 promoter. The target patients are the people with colorectal cancer who have positive MLH1 IHC or MSI high results. Promoter methylation of MLH1 can help to rule out Lynch syndrome in colorectal cancer patients, as well as women with endometrial cancer. Lynch syndrome is most frequently caused by inherited germline mutation of one or more of the DNA mismatch repair (MMR) genes (MLH1, MSH2, MSH6, PMS2). The current NCCN guideline recommended testing for loss of protein expression of these MMR genes using immunohistochemistry (IHC) or microsatellite instability by PCR. MLH1 is the protein most often found to be downregulated or completely absent, often in combination with PMS2. This loss of expression of MLH1 can either be the result of a germline mutation(s) in the MLH1 gene (indicating Lynch syndrome), or due to promoter methylation (indicating a sporadic CRC). Few cases exist MLH1 germline methylation in Lynch syndrome. Usually there is 27.7-77.2% of concordance between BRAF mutation and MLH1 methylation confirming sporadic CRC.




The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.