Tumor Antigens are Most Useful for Monitoring
Tumor antigens are most useful for monitoring disease response to treatment and detecting recurrence, rather than for diagnosis, screening, or classification of cancers. 1, 2
Evidence Supporting Monitoring as Primary Use
Colorectal Cancer
- The American Society of Clinical Oncology (ASCO) recommends carcinoembryonic antigen (CEA) as the marker of choice for monitoring response of metastatic colorectal cancer to systemic therapy 1
- CEA should be measured every 3 months for stage II and III disease for at least 3 years if the patient is a potential candidate for surgery or chemotherapy of metastatic disease 1
- For patients with metastatic disease, CEA should be measured every 1-3 months during active treatment 2
- Two consecutive rising CEA values above baseline suggest disease progression, even without radiographic confirmation 2
Breast Cancer
- CA 15-3 and CA 27.29 levels correlate with disease response during treatment for metastatic breast cancer 1
- Measurement of CA 15-3 during treatment follow-up in patients with metastatic disease is useful in evaluating treatment response 1
- Changes in marker levels of more than 50% correlate with clinical changes in disease status 3
- In 87.5% of cases with clinically progressive disease, one or both marker levels increased by more than 50% from previous levels 3
Limitations for Other Uses
Diagnosis
- CA 15-3 should not be used as a diagnostic test due to low sensitivity 1
- With the exception of PSA, tumor markers do not have sufficient sensitivity or specificity for use in diagnosis 4
- The sensitivity of tumor markers in the diagnosis of local recurrence is poor 1
Screening
- Tumor markers generally lack sufficient sensitivity or specificity for screening purposes 4
- The early detection of metastatic disease using tumor markers alone does not benefit the patient in terms of overall survival or time to the appearance of clinical signs 1
Classification
- While tumor markers may help identify the tissue of origin in some cases (like AFP for hepatocellular carcinoma), they are not reliable enough for definitive cancer classification 4
- There is no justification for routinely measuring multiple markers for classification purposes 1
Clinical Application Algorithm
Baseline measurement: Obtain tumor marker levels before initiating treatment to establish a reference value 1, 2
Regular monitoring during treatment:
Interpretation of results:
Response to elevated levels:
- Confirm with imaging studies
- Consider treatment modification if confirmed progression
Caveats and Pitfalls
- Tumor marker elevation can occur in benign conditions (inflammation, organ dysfunction) 2
- Transient elevations may occur during the first 4-6 weeks of chemotherapy 2
- Clinical examination and imaging should not be replaced by tumor marker monitoring alone 1
- Different markers have varying sensitivities and specificities for different cancer types 4
Tumor markers serve as valuable tools primarily for monitoring disease status and treatment response, with limited utility for diagnosis, screening, or classification of cancers.