Test Code CEA Carcinoembryonic Antigen (CEA)
Additional Codes
Cerner |
NextGen |
Carcinoembryonic Antigen (CEA) |
Carcinoembryonic Antigen (CEA) |
Alternate Name(s)
Embryonic Carcinoma Antigen
Methodology
(Ortho) Chemiluminescence-Immunometric
Patient Preparation
None
Collection Instructions
Standard phlebotomy practices.
Centrifuge specimens and remove serum from cells within 2 hours of collection.
Specimen Requirements
Container |
|
||||||||||||
Stability |
|
||||||||||||
Rejection Criteria |
Lipemic or Turbid Specimens |
Result Reporting and Reference Values
Reported in ng/mL
Category |
Low |
High |
Nonsmokers |
0 |
3.0 |
Smokers |
0 |
5.0 |
Reflex Testing
None
Limitations
- Values obtained with different assay methods may be different and cannot be used interchangeably.
- Test results cannot be interpreted as absolute evidence for the presence or absence of malignant disease.
Useful For
To aid in the prognosis and management of cancer patients in whom changing concentrations of CEA are observed.
Increased levels may be found in patients with primary colorectal cancer or other malignancies including medullary thyroid carcinoma and breast, gastrointestinal tract, liver, lung, ovarian, pancreatic, and prostatic cancers.
Serial monitoring of CEA should begin prior to therapy to verify post therapy decrease in concentration and to establish a baseline for evaluating possible recurrence. Levels generally return to normal within 1 to 4 months after removal of cancerous tissue.