Test Code LAB1211 Alpha-Fetoprotein (AFP) Tumor Marker
Additional Codes
Test Name in EPIC | EPIC Test Code | Mnemonic |
---|---|---|
ALPHA-FETOPROTEIN TUMOR MARKER | LAB1211 | AFP TM |
Test Alias
AFP
Useful For/Utility
Follow-up management of patients undergoing cancer therapy, especially for testicular and ovarian tumors and for hepatocellular carcinoma
Often used in conjunction with human chorionic gonadotropin.
This test is not recommended as a screening procedure for cancer detection in the general population.
This test is not intended for the detection of neural tube defects.
This test is not useful for patients with pure seminoma or dysgerminoma.
Methodology
Chemiluminescent Microparticle Immunoassay (CMIA)
Clinical Information
It has been shown that elevation of serum AFP above values typically found in healthy individuals occurs in several malignant diseases, most notably nonseminomatous testicular cancer and primary hepatocellular carcinoma. In the case of nonseminomatous testicular cancer, a direct relationship has been observed between the incidence of elevated AFP levels and the stage of disease. Elevated AFP levels have also been observed in patients diagnosed as having seminoma with nonseminomatous elements but have not been observed in patients with pure seminoma. Human chorionic gonadotropin (hCG) and AFP are also important prognostic indicators of survival rate among patients with advanced nonseminomatous germ cell testicular tumors.
For patients in clinical remission following treatment of nonseminomatous testicular cancers, AFP levels generally decrease. Post-operative AFP values which fail to return to normal strongly suggest the presence of residual tumor. Tumor recurrence is often accompanied by a rise in AFP before progressive disease is clinically evident. Greater than 70% of patients with primary hepatocellular carcinoma have been reported to have elevated levels of serum AFP. Elevated AFP levels have occasionally been found in association with gastrointestinal tract cancers with and without liver metastases and only rarely in other malignancies. Serum AFP has been found to be elevated during pregnancy, in diseases such as ataxia telangiectasia, hereditary tyrosinemia, teratocarcinoma and in benign hepatic conditions such as acute viral hepatitis, chronic active hepatitis and cirrhosis. Elevation of serum AFP in benign hepatic diseases is usually transient.
AFP testing is not recommended as a screening procedure to detect cancer in the general population.
Specimen Requirements
Preferred:
Specimen Type: Serum
Container/Tube: Serum gel SST
Specimen Volume: 0.5 mL
Specimen Minimum Volume: 0.5 mL
Collection Instructions:
1. Hemolyzed specimen is not acceptable.
2. Separate plasma from cells within 2 hours of draw.
Additional Information:
1. Avoid repeated freeze/thaw cycles.
2. Label specimen appropriately (serum).
Alternate:
Specimen Type: Serum
Container/Tube: Serum gel
Specimen Volume: 0.5 mL
Specimen Minimum Volume: 0.15 mL
Collection Instructions:
1. Hemolyzed specimen is not acceptable.
2. Separate plasma from cells within 2 hours of draw.
Additional Information:
1. Avoid repeated freeze/thaw cycles.
2. Label specimen appropriately (serum).
Specimen Transport Temperature
Refrigerate 5 days/Ambient 3 days OK/Frozen OK
Day(s) Test Set Up
Monday through Sunday
Performing Laboratory
Chemistry -
SMDC Clinical Lab
Test Classification and CPT Coding
82105
Reference Values
0-8.8 ng/mL
Reference values are for non-pregnant subjects only; fetal production of AFP elevates values in pregnant women.