Carcinoembryonic Antigen
Also known as: CEA
Use
Measurement of CEA has been shown to be clinically relevant in the management of patients with colorectal, breast, lung, prostatic, pancreatic, and ovarian carcinomas. CEA levels can assist in monitoring disease progression or response to therapy. It is important to note that smokers may exhibit slightly elevated levels of CEA. However, the CEA assay value, irrespective of the level, should not be taken as evidence for the presence or absence of malignant disease and is not recommended for use as a screening test for detecting cancer in the general population.
Special Instructions
Specimen should be allowed to clot completely at room temperature. Serum must be separated from cells as soon as possible or within 2 hours of collection, and transferred to an ARUP Standard Transport Tube.
Limitations
Results from different test methods or kits cannot be used interchangeably. The CEA assay should not be used as a standalone diagnostic tool for cancer presence or absence and is not recommended for screening the general population for cancer.
Methodology
Immunoassay (ECLIA)
Biomarkers
LOINC Codes
- 2039-6
Result Turnaround Time
1 day
Related Documents
For more information, please review the documents below
Specimen
Serum
Volume
1 mL
Minimum Volume
0.6 mL
Container
ARUP Standard Transport Tube
Collection Instructions
Allow specimen to clot completely at room temperature. Separate serum from cells ASAP or within 2 hours of collection. Transfer to an ARUP Standard Transport Tube.
Causes for Rejection
Body Fluid (refer to Carcinoembryonic Antigen, Fluid, ARUP test code 0020742).
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | 7 days |
| Refrigerated | 2 weeks |
| Frozen | 6 months |
