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Beta-core fragment (beta-core/UGF/UGP), a tumor marker: a 7-year report
1Department of Obstetrics and Gynecology, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Gynecologic Oncology
|February 1, 1996
Summary
Urine beta-core/UGF/UGP shows promise as a stage-dependent tumor marker for gynecological cancers, with sensitivity increasing with malignancy stage in both retrospective and prospective studies.
Area of Science:
- Gynecology
- Oncology
- Biochemistry
Background:
- Urine beta-core fragment, also known as beta-core/UGF/UGP, has been investigated as a potential biomarker for gynecological cancers since 1988.
- Three commercial immunoassays are currently available for its detection.
Purpose of the Study:
- To compare three commercial immunoassays for urine beta-core/UGF/UGP.
- To establish cutoff limits for the marker.
- To evaluate the marker's sensitivity and specificity in retrospective and prospective studies of gynecological cancer patients.
Main Methods:
- A retrospective study analyzed 486 urine samples from gynecological cancer patients and controls.
- A prospective study monitored 548 new patients at a Gynecology Oncology Clinic over 16 months.
- The Ciba-Corning kit was used to measure beta-core/UGF/UGP levels in all samples.
Main Results:
- Elevated beta-core/UGF/UGP levels (>1.9 ng/ml) were found in 11% of healthy individuals and 11% with benign gynecological disease.
- In retrospective and prospective studies, elevated levels were detected in 50% and 48% of gynecological cancer samples, respectively.
- Sensitivity increased with advancing cancer stage, ranging from 28-29% for stage I to 68-77% for stage IV.
Conclusions:
- Urine beta-core/UGF/UGP demonstrates potential as a general, stage-dependent tumor marker for gynecological cancers.
- The marker's sensitivity is higher for advanced-stage malignancies.
- Findings from both retrospective and prospective studies confirm its utility and suggest a definitive false-positive rate and sensitivity.