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Cancer Antigen (CA) 125

Code:10004|CPT:86304|LOINC:10334-1

Synonyms
CA 125Second Generation Assay
IncludesCancer Antigen (CA) 125

Analysis details

Methodology

  • Electrochemiluminescence immunoassay (ECLIA)

Expected Turnaround Time

1 day

Special Instructions

  • Do not smoke during the 30 minutes before the blood draw.
  • For serial follow‑up, use the same assay methodology each time; avoid comparing results produced by different methods.
  • If taking high‑dose biotin supplements, stop for at least 72 hours before specimen collection.

How to use

Cancer Antigen (CA) 125, also referred to as CA‑125, is used to aid diagnosis of epithelial ovarian cancer in the appropriate clinical context, to monitor disease course and therapeutic response, and to detect ovarian cancer recurrence. When combined with other tumor markers such as CA 72‑4 or HE4, overall diagnostic sensitivity may be higher.

Limitations

Ovarian cancer represents approximately 4% to 6% of female malignancies and frequently presents without specific early symptoms. Tumor markers complement physical examination and imaging in this setting. CA 125 is a high–molecular‑weight glycoprotein present on ovarian epithelial tumor cells and also found in normal tissues, including pericardium, pleura, peritoneum, endometrium, and testes. Marked serum elevations are common in ovarian malignancy and occur less often with other cancers (eg, endometrial, colorectal, lung, breast, pancreatic). Because expression and serum increases are also seen in healthy women and in benign or inflammatory disorders—such as benign ovarian and uterine conditions, endometriosis, peritonitis, pleuritis, chronic hepatitis or cirrhosis, and chronic pancreatitis—interpretation requires clinical context. Persistent elevation in postmenopausal women is more strongly associated with malignant epithelial ovarian tumors. CA 72‑4 can be elevated in mucinous ovarian carcinoma and in other adenocarcinomas; assessing CA 125 together with CA 72‑4 has been reported to raise diagnostic sensitivity to approximately 73%.

Reference interval
MaleFemale
0–200–35
IndicationsWorkup of a possible ovarian tumor, Assisting in distinguishing benign from malignant ovarian masses, Postoperative evaluation of therapeutic effectiveness, Assessment when metastatic spread is suspected, Testing in individuals with high‑risk human papillomavirus identified by PCR

Possible Causes of Abnormal Results

Decreased levels

  • biotin

Specimen Requirements

SpecimenSerum
ContainerGold/Tiger Top (SST, Gel Separator)
Volume1 mL (min 0.7 mL)
Storage InstructionsRoom temperature, Refrigerated, Frozen

References

Kozachenko VP. Treatment of patients with ovarian cancer. Russian Medical Journal. 2003;26:1458.

Urmanceeva AF, Meshkova IE. Issues of epidemiology and diagnosis of ovarian cancer. Medical Academy of Postgraduate Education, N.N. Petrov Research Institute of Oncology, St. Petersburg.

Cancer Incidence in Five Continents. IARC Scientific Publications. Lyon; 1997; Vol. 7:143.