Test Code FLCA125 Fluid Cancer Antigen 125
Specimen and Container/Tube
Specimen Type: Fluid
Preferred Specimen: Non-additive/Non-gel plastic containers with tight-fitting leak-proof lids
Other Acceptable specimens: Sterile Plastic Container, Sterile Clean Glass Container
Specimen Handling and Transport Instructions
UCMC Onsite Instructions:
Collect specimen per standard collection procedure and send to laboratory immediately.
UCMC Offsite and UC MedLab Outreach Instructions:
- Samples should be collected in sterile container.
- No preservatives or additives.
- Centrifuge specimens at >2500 x g for 10 minutes at room temperature.
- Aliquot sample into plastic transport tube containing a minimum of 1.0 mL of specimen.
- Samples must be sent refrigerated at 2-8oC.
Rejection Criteria
- Common specimen rejected situations include: incorrect specimen type, insufficient volume, missing or incomplete specimen identifiers, incorrect specimen transport, or specimens outside stability limits.
- Specimens that are clotted, viscous or grossly hemolyzed.
- Specimens that are collected with preservatives or additives.
Reference Values
Test |
Age |
Sex |
Reference Range |
CA 125 |
All |
All |
N/A |
Test method analytical performance not validated for specimen type. No reference range available. The test result must be interpreted in conjunction with the clinical context of the patient.
Critical Values
Analyte |
Unit |
Low |
High |
Age |
N/A |
N/A |
N/A |
N/A |
N/A |
CPT Codes
86304
LOINC Codes
N/A
Volume
Preferred Volume: 2.0 mL
Minimum Volume: 1.0 mL
Specimen Stability
Storage Temperature |
Stability |
Room temperature |
8 hours |
Refrigerated |
5 days |
Frozen |
30 days |
Collection Instructions
- Collect specimen per standard laboratory collection procedures.
- No preservatives or additives.
Test Components
Cancer Antigen 125
Clinical Indications
Differentiate between malignant vs. non-malignant causes of fluid accumulation.
Methodology
Electrochemiluminescence immunoassay (ECLIA) (Roche Diagnostics)
Additional Information
- No reference range avaliable. The test results should always be assessed in conjunction with patient's medical history, clinical examination and other findings.
- The measured tumor marker value of a patient's sample can vary depending on the testing procedure and method used. Tumor marker values determined on patient samples by different testing procedures or methodologies cannot be directly compared with one another and could be the cause of erroneous medical interpretations.
- Results verified by manual dilutions.
Turnaround Time
Turnaround times are relative to the time the specimen is received in the test laboratory.
STAT Turnaround Time: Not Available as STAT test
Routine Turnaround Time: up to 4 hours
Testing Schedule: 24/7
Synonyms/Keyword Search
N/A
Last Review Date
1/26/23