Test Overview
Test Methodology

Chemiluminescent Immunoassay (CLIA)

Test Usage

Follow-up management of patients undergoing cancer therapy, especially for ovarian carcinoma. Consistently rising CA 125 results may be associated with malignant disease and poor response to therapy; declining values may be indicative of a favorable response to therapy.

Reference Range *

* Reference ranges may change over time. Please refer to the original patient report when evaluating results.

Test Limitations

CA 125 concentrations are elevated in 1-2% of healthy individuals and may be elevated in diseases other than ovarian cancer, including benign and malginant disorders. CA 125 is NOT a cancer screening test.

Test Details
Days Set Up
Daily, 24 hours
Analytic Time

4 hours

Soft Order Code
CA125
MiChart Code
CA 125
Synonyms
  • Cancer Antigen 125
  • DM70K Replacement Assay
  • Ovarian Cancer Tumor Marker
Laboratory
Chemical Pathology
Section
Automation
Specimen Requirements
Collection Instructions

Collect specimen in an SST or red top tube. Refrigerate and send intact specimen within 8 hours of collection. Alternatively, centrifuge, aliquot serum into a plastic vial and refrigerate up to 24 hours at 2-8C or freeze at -20C for longer storage.

Alternate Specimen

Red Top Tube

Normal Volume

0.5 mL serum

Minimum Volume

0.25 mL serum

Additional Information

Tested by a chemiluminescent immunoassay manufactured by Siemens Healthineers, performed on Atellica IM system. Results determined from different manufacturers and/or methods may not be comparable.

Billing
CPT Code
86304
Fee Code
32031
LOINC
10334-1
NY State Approved
No