ARUP's Laboratory Test Directory
| 0080464: Cancer Antigen-Breast (CA 15-3) |
| Test Mnemonic: CA-BREAST | |
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#ExistMethodology>
Methodology: Electrochemiluminescent Immunoassay
*ExistMethodology> #ExistPerformed> Performed: Sun-Sat *ExistPerformed> #ExistReported> Reported: Within 24 hours *ExistReported> |
| Specimen Required: | |
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#ExistCollect>
Collect: One 4 mL SST or PST. Also acceptable: green (sodium or lithium heparin), lavender (EDTA), or pink (K2EDTA).
*ExistCollect> #ExistTransport> Transport: 1 mL serum or plasma at 2-8°C. (Min: 0.5 mL) Submit specimen in an ARUP Standard Transport Tube. *ExistTransport> #ExistPedCollectTransport> Pediatric Collection/Transport: 0.2 mL serum or plasma at 2-8°C. *ExistPedCollectTransport> #ExistRemarks> Remarks: Allow specimen to clot completely at room temperature. Separate serum or plasma from cells ASAP. *ExistRemarks> #ExistStability> Stability: After separation from cells: Ambient: 8 hours; Refrigerated: 5 days; Frozen: 3 months *ExistStability> |
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| Reference Interval: |
| #ExistRefRange> 0-31 U/mL *ExistRefRange> |
| Interpretive Data: | |
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#ExistInterpData>
The Roche Modular E170 CA 15-3 electrochemiluminescent immunoassay is used. Results obtained with different methods or kits cannot be used interchangeably. The CA 15-3 assay is used to aid in the management of Stage II and III breast cancer patients. Serial testing for patient CA 15-3 assay values should be used in conjunction with other clinical methods for monitoring breast cancer. Patients with confirmed breast carcinoma frequently have CA 15-3 assay values in the same range as healthy individuals. Elevations may be observed in patients with nonmalignant disease. For these reasons, a CA 15-3 assay value, regardless of level, should not be interpreted as absolute evidence of the presence or absence of malignant disease.
*ExistInterpData> |
| CPT Code(s): | |
| 86300 |