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Department

Biochemistry

Preferred Sample Type

Carcino Embryonic Antigen (CEA)

Suitable Specimen Types

  • Serum
  • EDTA Plasma
  • Li Hep Plasma
5-10 mL vacutainer (minimum sample volume 200 uL)

Sample Processing in Laboratory

Usual

Sample Preparation

Centrifuge

Turnaround Time

7 days

Sample Stability

Stable at 4 ºC for up to seven days. For longer periods store the serum at -20 ºC.

Carcino Embryonic Antigen (CEA)

General Information

Carcino Embryonic Antigen (CEA) is a 200 kDa glycoprotein which appears to have a role in cell adhesion and inhibition of apoptosis. It can be elevated in any advanced adenocarcinoma, i.e., where distant metastases are present. CEA is almost never elevated in early malignancy.

In addition, slight to moderate elevations (i.e. > 10 ug/L) of CEA can be seen in 20-50% of benign diseases of the intestine, the pancreas, the liver, the kidney and the lungs (e.g. hepatitis, cirrhosis, alcoholic liver disease, obstructive jaundice, ulcerative colitis, Crohn’s disease, pancreatitis, bronchitis, emphysema and renal disease). Slight elevations may also occur in apparently healthy individuals who smoke.

CEA is primarily used for the monitoring of patients with colorectal carcinoma. Specifically:

  • In surveillance following curative resection of colorectal cancer.
  • In monitoring therapy in advanced colorectal cancer. This is especially important when disease cannot be evaluated by standard criteria.

 

Caution should be used when interpreting increasing CEA concentrations during the early phase of systemic treatment as certain treatments (e.g., 5-fluorouracil and levamisole; oxaliplatin) can cause transient elevations in CEA levels in the absence of disease progression.

CEA should not be used to screen for colorectal cancer.

Patient Preparation

Samples from patients receiving high biotin doses (i.e. >5 mg/day) should be taken at least 8 hours post dose.

Please inform the laboratory if the patient has been treated with monoclonal mouse antibodies or may have received them for diagnostic purposes.

Notes

Samples should be clot free and free of red blood cells or other particulate matter. The presence of fibrin may cause erroneous results.

 

Pathology Harmony have recently issued guidance on appropriate tumour marker requesting.  For information please click on the following link:

http://www.pathologyharmony.co.uk/harmony-bookmark-v7.pdf


If you would like some copies of the bookmark please contact the Duty Biochemist (bleep 2506).

Reference Range

Reference Range < 5 ug/L

Specifications

  • EQA Scheme?: Yes
  • EQA Status: NEQAS