Test ID SCCA Squamous Cell Carcinoma Antigen, Serum
Specimen Required
Collection Container/Tube: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 0.5 mL
Collection Information: Centrifuge and aliquot serum into a plastic vial. Do not submit in original tube.
Secondary ID
610033Useful For
Aiding in the evaluation and monitoring of squamous cell carcinoma of the head and neck, lung, and cervix
This test should not be used to screen for carcinoma or other disorders including those of the liver, lung, or skin.
Method Name
Immunofluorescent Assay (IFA)
Reporting Name
Squamous Cell Carcinoma Antigen, SSpecimen Type
Serum SSTSpecimen Minimum Volume
0.2 mL
Specimen Stability Information
Specimen Type | Temperature | Time |
---|---|---|
Serum SST | Frozen (preferred) | 90 days |
Ambient | 7 days | |
Refrigerated | 7 days |
Clinical Information
Squamous cell carcinoma (SCC) of the skin is the second most common form of skin cancer, characterized by abnormal, accelerated cellular growth. SCC antigen (SCCA) represents a subfraction of tumor-associated antigens related to squamous cell carcinoma and is used as a serum tumor marker for squamous cell carcinoma of the head and neck, lung (including esophagus), and other types of SCC. Additionally, associations between serum SCCA concentrations and tumor stage, size, and progression have been observed in SCCs of the cervix and esophagus. SCC is the most common histological type of cervical cancer, accounting for more than 70% of cervical cancer cases in the United States.
SCCA is a cytoplasmic glycoprotein found in normal squamous epithelia and elevated concentrations in serum from patients with SCCs. SCCA exists as two isoforms, SCCA1 and SCCA2, which are 91% identical at the amino acid level. Total SCCA assays (which measure both SCCA 1 and 2), like this assay, may be used in conjunction with clinical evaluation in the follow-up/monitoring of patients with SCC of the cervix, lung, head and neck, and esophagus.
SCCA serum concentrations may be used for monitoring response to treatment in patients with cervical cancer. Notably, in 46% to 92% of patients who experience recurrence, an elevated level of SCCA after treatment was observed before the clinical manifestation of relapse, with a median lead time of 2 to 8 months. While pretreatment serum SCCA concentrations in patients with cervical cancer are more correlated with tumor burden and prognosis, there is some evidence that it may also help to differentiate patients with and without risk for lymph node metastasis. Furthermore, it has been shown that SCCA is a useful marker in follow-up and therapy monitoring, and increasing SCCA levels may predict relapse.
Increased serum SCCA values have also been associated with benign inflammatory diseases, including various skin disorders, such as psoriasis and atopic dermatitis, in addition to inflammatory disorders, such as asthma. In one report, 70% of patients with psoriasis and dermatitis had SCCA concentrations greater than 2.4 ng/mL (radioimmunoassay reference value), with some patients having SCCA concentrations between 20 and 60 ng/mL. Another study found that median concentrations of SCCA2 were higher in psoriasis (2.7 ng/mL, interquartile range: 1.25-7.75 ng/mL) than in controls (0.7 ng/mL, interquartile range: 0.40-0.80 ng/mL).
Reference Values
Males: ≤2.00 mcg/L
Females: ≤1.67 mcg/L
Reference values have not been established for patients younger than 18 years old.
Cautions
Do not interpret serum squamous cell carcinoma antigen (SCCA) concentrations as absolute evidence of the presence or the absence of malignant disease. Use serum SCCA results in conjunction with information from the clinical evaluation of the patient and other diagnostic procedures.
Elevated concentrations may also occur in cases of kidney insufficiency, skin disorders such as psoriasis, or inflammatory lung disease such as asthma.
Specimens with extremely elevated SCCA concentrations (>2200 mcg/L) have the potential to exhibit a "hook effect" and appear to have markedly lower SCCA concentrations in the absence of specimen dilution.
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. Caution should be used in interpretation of results, and the laboratory should be alerted if the result does not correlate with the clinical presentation.
SCCA concentration determinations are method dependent. Values obtained with different assay methods or kits may be different and cannot be used interchangeably.
Day(s) Performed
Tuesday
Report Available
Same day/1 day to 7 daysPerforming Laboratory

Test Classification
This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.CPT Code Information
86316