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Serum/Plasma Tumor Marker Panel (Cancer Ag 724) – Multiplex Immunoassay

Published: August 9, 2026Updated: August 17, 2026

This test measures multiple tumor markers in your blood to help detect or monitor certain cancers, including prostate, breast, lung, and other solid tumors. Results may assist in screening, diagnosis, or treatment planning.

Quick summary

["This blood test helps track cancer progression or response to treatment by checking for specific proteins linked to cancer cells."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 17, 2026Editorial policy

Key facts at a glance

LOINC
2015-6
Short code
CA724
Synonyms
Cancer Ag72-4 SerPl Ql
Category
chemistry
Sample
serum
Container
Serum separator tube (SST) or red-top tube without anticoagulant. Plasma may be collected in lithium heparin or EDTA tubes if serum is unavailable.
Units
N/A
Ref low
0
Ref high
6
Critical range
0.5 N/A – —
Fasting
false
Population
adult
Sex
all
Age range
18–99 years
Method
Electrochemiluminescence Immunoassay (ECLIA)
CPT
86316
SNOMED
115341000
Specimen volume
1.0 mL serum or plasma (minimum 0.5 mL)
Stability
Room temperature: 8 hours; Refrigerated (2-8°C): 7 days; Frozen (-20°C or below): 3 months. Avoid repeated freeze-thaw cycles.
Hemolysis max
50
Lipemia max
100
Icterus max
25
TAT
4–24 hours
Order
routine

This test measures specific substances, markers, or activity levels in your body that help your healthcare provider understand how well certain organs and systems are working. The results can help detect a health problem early, diagnose a condition, or monitor how well a treatment is working over time.

The Cancer Ag 724 panel includes several biomarkers detected through a multiplex immunoassay. These markers may include proteins like prostate-specific antigen (PSA), carbohydrate antigen 125 (CA-125), carcinoembryonic antigen (CEA), and others depending on the specific assay configuration. Each marker reflects different cancer types or stages, and results are interpreted by your healthcare provider in context with your medical history and symptoms.

Your healthcare provider may order this test if you have symptoms that need a closer look, if you have an ongoing condition that requires regular monitoring, or as part of a routine checkup to screen for potential health problems before symptoms appear.

Your doctor may order this test if you have a history of cancer, symptoms suggestive of cancer (e.g., unexplained weight loss, fatigue, or persistent pain), or if you’re undergoing cancer surveillance or treatment monitoring. It can also be part of a general cancer screening or follow-up for known cancer types.

The test works by analyzing a small sample from your body, such as blood, urine, or tissue, or by measuring signals from your body with specialized equipment. A laboratory or testing device then compares your results with established reference ranges to show whether your values fall within the expected range.

A blood sample is drawn, and the serum or plasma is analyzed using a highly sensitive immunoassay technique. This method detects and quantifies tumor markers with high precision, allowing for early detection or monitoring of cancer activity.

Before the test, follow any instructions from your healthcare provider, which may include fasting for a set number of hours, avoiding certain foods, medications, or supplements, or drinking extra water. Tell your provider about all medications you take and any allergies you have, and plan to arrive a little early to complete any paperwork.

No special preparation is typically needed, but you may be asked to fast for 8–12 hours before the test if instructed by your provider. Wear comfortable clothing and plan to rest after the blood draw. Avoid strenuous activity the day of the test.

Reference range

Negative: <6.0 U/mL; Equivocal: 6.0-8.0 U/mL; Positive: >8.0 U/mL (manufacturer-dependent; verify with reporting laboratory)N/A

Specimen: serum

No special patient preparation required. Fasting is not necessary. Specimen should be collected prior to administration of biotin or after a washout period of at least 8 hours if patient is on high-dose biotin therapy (>5 mg/day), as biotin may interfere with immunoassay results.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

Clinical Significance

Short name

Cancer Ag 724 Panel

Frequently asked questions

How can elevated or abnormal results affect my treatment plan?
How often should I get this test, and does the schedule depend on my age or overall health?
What if my results are abnormal?
No, this test does not replace imaging or biopsies. It provides supporting information, but your doctor may still order X-rays, CT scans, MRI, ultrasound, or a biopsy when a closer look at tissues or structures is needed to confirm a diagnosis.
Can lifestyle changes affect my test results?
Some lifestyle factors, such as diet, exercise, or medications (e.g., certain supplements), may influence marker levels. For example, high-fat diets or certain medications could temporarily alter PSA or other marker readings. Discuss your lifestyle and medications with your doctor to ensure accurate interpretation of results.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 17, 2026. · Read our editorial policy