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Last updated: 11/24/2009

Normal results

Reference ranges for tumor markers will vary from one laboratory to another because different antibodies and calibrators are used by various test systems. The values below are representative of normal values or cutoffs for commonly measured tumor markers.

  • Alpha-fetoprotein...

    (AFP): Less than 15 ng/L in men and nonpregnant women. Levels greater than 1,000 ng/L indicate malignant disease (except in pregnancy).
  • CA125: Less than 35 U/mL.
  • Carcinoembryonic antigen (CEA): Less than 3 ?g/L for nonsmokers and less than 5 ?g/L for smokers.
  • Estrogen receptor: Less than 6 fmol/mg protein is negative; greater than 10 fmol/mg protein is positive.
  • Human chorionic gonadotropin (HCG): Less than 20 IU/L for males and non-pregnant females. Greater than 100,00 IU/L indicates trophoblastic tumor.
  • Progesterone receptor: Less than 6 fmol/mg protein is negative. Greater than 10 fmol/mg protein is positive.
  • Prostate specific antigen (PSA): Less than 4 ng/L.

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Other Information

A tumor marker is a substance found in the blood, urine, or body tissues that can be elevated in cancer, among other tissue types. There are many different tumor markers, each indicative of a particular disease process, and they are used in oncology to help detect the presence of cancer. An elevated level of a tumor marker can indicate cancer; however, there can also be other causes of the elevation.

The hook effect (also known as high dose hook effect) is an artifact of tumor marker immunoassay kits, that causes the reported quantity of tumor marker to be incorrectly low when the quantity is high. An undetected hook effect may cause delayed recognition of a tumor. The hook effect can be detected by analyzing serial dilutions. Absent hook effect, reported quantities of tumor marker in a serial dilution should be proportional to the dilution.

If repeated measurements of tumor marker are needed, some clinical testing laboratories provide a special reporting mechanism, a serial monitor, that links test results and other data pertaining to the person being tested. This requires a unique identifier for the person. In the United States commonly a Social Security number is used for this. One important function of this mechanism is to ensure that each test is performed using the same assay kit. For example, for AFP many different commercial assay kits, based on different technologies, are available. AFP measurements obtained using different assay kits are not comparable unless special calculations are performed.

Interlaboratory proficiency testing for tumor marker tests, and for clinical tests more generally, is an emerging field.In the United States, New York state is prominent in advocating such research.


From http://en.wikipedia.org/wiki/Tumor_marker#Application_and_Interpretation

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