SERUM ALPHA-L-FUCOSIDASE ENZYME-ACTIVITY IN OVARIAN AND OTHER FEMALE GENITAL-TRACT TUMORS

Citation
H. Abdelaleem et al., SERUM ALPHA-L-FUCOSIDASE ENZYME-ACTIVITY IN OVARIAN AND OTHER FEMALE GENITAL-TRACT TUMORS, International journal of gynaecology and obstetrics, 55(3), 1996, pp. 273-279
Citations number
11
Categorie Soggetti
Obsetric & Gynecology
ISSN journal
00207292
Volume
55
Issue
3
Year of publication
1996
Pages
273 - 279
Database
ISI
SICI code
0020-7292(1996)55:3<273:SAEIOA>2.0.ZU;2-N
Abstract
Objectives: To assess the value of serum alpha-L-fucosidase as a tumor marker in the diagnosis of ovarian and other female genital tract tum ors. Methods: One-hundred fifty-one patients were studied; 101 had dif ferent genital tract tumors (malignant ovarian tumors (48), carcinoma of the cervix (13), endometrial carcinoma (6), carcinoma of the vulva (6) and benign tumors (28)), A control group of 50 healthy female pati ents was included. Serum alpha-L-fucosidase activity was determined in all patients and controls. Serum CA 125 level was also determined in patients with malignant ovarian tumors. Results: Patients with maligna nt ovarian tumors showed the lowest level of alpha-L-fucosidase activi ty in comparison to other malignant and benign tumors of the female ge nital tract and also in comparison to control group. The majority of o varian carcinoma patients (90%) had a serum level of < 275 u/ml of alp ha-L-fucosidase activity, while more than 90% of the control group and other genital tumors had a serum level of > 275 u/ml. The sensitivity and specificity of serum alpha-L-fucosidase activity in diagnosing ep ithelial ovarian tumors were 88.5% and 98%, respectively (using a cut- off level of < 275 u/ml). The corresponding figures for CA 125 were 96 .2% and 100% (using a cut-off level of > 35 u/ml). Conclusions: Serum alpha-L-fucosidase enzyme activity can be useful as a tumor marker in diagnosing advanced malignant epithelial ovarian tumors. Its sensitivi ty and specificity are comparable to CA 125. However, there is lack of data to support its usefulness in the diagnosis of early stage diseas e (Stage 1). The cost of doing the test is one-third that of CA 125 an d the test can be more widely applied in developing countries. Copyrig ht (C) 1996 International Federation of Gynecology and Obstetrics.