Test Code LAB3215 Human Epididymis Protein 4, Serum
Useful For
Aiding in monitoring patients with treated epithelial ovarian cancer for recurrence or progression
This test should not be used as a screening test for ovarian cancer.
Reporting Name
HE4, SSpecimen Type
SerumSpecimen Required
Patient Preparation: For 12 hours before specimen collection, patient should not take multivitamins or dietary supplements (eg, hair, skin, and nail supplements) containing biotin (vitamin B7).
Supplies: Sarstedt Aliquot Tube, 5 mL (T914)
Collection Container/Tube:
Preferred: Serum gel
Acceptable: Red top
Submission Container: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Minimum Volume
0.75 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum | Frozen (preferred) | 84 days |
Refrigerated | 7 days |
Reject Due To
Gross hemolysis | Reject |
Gross lipemia | OK |
Reference Values
Females: ≤140 pmol/L
Males: Not applicable
Cautions
Results cannot be interpreted as absolute evidence of the presence or absence of malignant ovarian disease, because mild elevations of human epididymis protein 4 (HE4) might also be present in individuals with benign gynecologic conditions (ovarian cysts, cystadenomas, leiomyomas, myomas, fibromas, and endometriosis), hypertension, congestive heart failure, and kidney or liver disease.
Serial testing for patient HE4 results should be used in conjunction with other clinical methods for monitoring ovarian cancer.
The use of this test in disease states other than ovarian cancer has not been clinically validated.
Serum markers are not specific for malignancy and values may vary by method. Values obtained with different assay methods cannot be used interchangeably. Correlation studies between this method and the previous enzyme-linked immunosorbent assay method show good correlation (correlation coefficient =0.92). However, this method will, on average, give 28% higher HE4 concentrations and individual patient results may vary more than would be calculated from the correlation equation.
Ideally, when changing methods, parallel testing using the old and new method allows for establishing the patient's HE4 baseline levels with the new method (rebaseline).
In rare cases, some individuals can develop antibodies to mouse or other animal antibodies (often referred to as human anti-mouse antibodies [HAMA] or heterophile antibodies), which may cause interference in some immunoassays. The presence of antibodies to streptavidin or ruthenium can rarely occur and may also interfere in this assay. Caution should be used in interpretation of results, and the laboratory should be alerted if the result does not correlate with the clinical presentation.
Day(s) Performed
Monday through Saturday
Report Available
1 to 3 daysPerforming Laboratory

Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.CPT Code Information
86305
LOINC Code Information
Test ID | Test Order Name | Order LOINC Value |
---|---|---|
HE4 | HE4, S | 55180-4 |
Result ID | Test Result Name | Result LOINC Value |
---|---|---|
HE4 | HE4, S | 55180-4 |
NY State Approved
YesMethod Name
Electrochemiluminescence Immunoassay (ECLIA)
Secondary ID
62137Forms
If not ordering electronically, complete, print, and send an Oncology Test Request (T729) with the specimen.