Analysis interpretation and preparation

The accuracy of tumor markers: a modern scientific view

Laboratory diagnostics of tumor marker accuracy

In modern oncology, laboratory diagnostics plays an extremely important role, and tumor markers have become one of the key tools in the early detection and monitoring of malignant neoplasms. However, the question of their accuracy remains debatable. None of the known markers is completely specific or sensitive, which creates the need to combine these tests with other methods - imaging, histological and molecular genetic.

Scientific determination of tumor marker accuracy

Accuracy in diagnostic tests is understood as an integrative indicator that combines:

  • Sensitivity — the probability of getting a positive result in a patient with cancer.

  • Specificity — the probability of obtaining a negative result in a healthy patient.

  • Predictive value (PPV/NPV) — the extent to which the results can be extrapolated to clinical practice, depending on the prevalence of the disease in the population.

International clinical guidelines (NCCN, ESMO, WHO) state that tumor markers are of limited value for primary screening, but are valuable in monitoring treatment and detecting relapses.

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Accuracy of basic tumor markers: clinical data

Tumor markerMain localization of tumorsMedium sensitivityAverage specificityScientific comments
PSA (prostate-specific antigen)Prostate cancer60–80%50–70%Also increases in benign hyperplasia; therefore, used in screening along with digital rectal examination and MRI
CA-125Ovarian cancer70–85%50–60%High values are possible with endometriosis and pelvic inflammatory disease.
CEA (carcinoembryonic antigen)Colorectal cancer, lung cancer40–70%60–80%Often elevated in smokers; not recommended for mass screening
AFP (alpha-fetoprotein)Hepatocellular carcinoma50–70%80–90%When combined with liver ultrasound, accuracy increases
CA 19-9Pancreatic cancer70–80%65–75%Often elevated in pancreatitis or cholestasis, so diagnostic value is limited

These data are summarized based on studies published in Journal of Clinical Oncology and recommendations Mayo Clinic.

Factors affecting the accuracy of tumor markers

  1. Biological variations — levels can vary depending on age, gender, and hormonal status.

  2. Comorbidities — inflammatory processes, infections, liver and kidney diseases can increase the indicators.

  3. Pharmacological effects — certain medications can change the levels of tumor markers.

  4. Methodological errors — sample collection, transportation and storage.

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Schematic diagram of tumor marker accuracy

Scientific discussions and perspectives

Modern oncology increasingly turning to multigene and molecular genetic tests, which, in combination with tumor markers, can increase diagnostic accuracy. Use biomarker panels, as well as liquid biopsy (analysis of circulating tumor DNA in the blood) may become a more promising method for early cancer detection in the future.

Practical conclusions for clinical practice

  • Tumor markers should not be used as the sole diagnostic tool.

  • The greatest value is in monitoring the course of the disease and assessing the effectiveness of therapy.

  • To increase accuracy, it is recommended to use combined diagnostic strategies (imaging + laboratory + histology).

  • Patients should understand: an elevated marker level is not a diagnosis, but a reason for further examination.

The accuracy of tumor markers has clear limitations, but when combined with modern diagnostic methods, they remain an important element of evidence-based medicine.

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