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Human tissue polypeptide antigen in breast cancer.
Journal of the National Cancer Institute
|December 1, 1979
Summary
Tissue polypeptide antigen (TPA) and carcinoembryonic antigen (CEA) show similar effectiveness as breast cancer tumor markers. Both markers were frequently elevated in patients with metastatic breast cancer, with TPA also showing elevated levels in some benign breast disease cases.
Area of Science:
- Oncology
- Biochemistry
- Medical Diagnostics
Background:
- Breast cancer diagnosis and monitoring rely on accurate tumor markers.
- Tissue polypeptide antigen (TPA) and carcinoembryonic antigen (CEA) are established tumor markers.
- Evaluating the comparative efficacy of TPA and CEA in breast cancer is crucial for clinical application.
Purpose of the Study:
- To simultaneously measure serum TPA and plasma CEA levels in breast cancer patients and control groups.
- To compare the diagnostic utility of TPA and CEA as tumor markers for breast cancer.
- To assess the correlation of TPA and CEA levels with disease stage, metastasis, and clinical course.
Main Methods:
- Simultaneous measurement of serum TPA and plasma CEA.
- Study population included 108 breast cancer patients, 40 healthy women, and 26 women with benign breast disease.
- Analysis of marker levels in primary, metastatic, and recurrent breast cancer, as well as benign conditions and healthy controls.
Main Results:
- TPA elevation observed in 53% of primary and 70% of metastatic breast cancer cases; CEA in 21% of primary and 61% of metastatic cases.
- TPA was elevated in 27% of benign breast disease cases, while CEA was not elevated.
- TPA elevation was more frequent in visceral metastasis. Both markers showed limited correlation with clinical course during palliative therapy.
Conclusions:
- Serum TPA and plasma CEA demonstrate comparable efficacy as tumor markers in breast cancer.
- TPA exhibits a higher rate of elevation in benign breast disease compared to CEA.
- TPA and CEA are valuable tools for monitoring breast cancer, particularly in metastatic disease.