It has been suggested that oestrogen replacement therapy is associated with
risk of epithelial ovarian cancer of the endometrioid type. Using data fro
m an Australian population-based case-control study, the relation between u
nopposed oestrogen replacement therapy and epithelial ovarian cancer, both
overall and according to histological type, was examined. A total of 793 el
igible incident cases of epithelial ovarian cancer diagnosed from 1990 to 1
993 among women living in Queensland, New South Wales and Victoria were ide
ntified. These were compared with 855 eligible female controls selected at
random from the electoral roll, stratified by age and geographic region. Tr
ained interviewers administered standard questionnaires to obtain detailed
reproductive and contraceptive histories, as well as details about hormone
replacement therapy and pelvic operations. No clear associations were obser
ved between use of hormone replacement therapy overall and risk of ovarian
cancer. Unopposed oestrogen replacement therapy was, however, associated wi
th a significant increase in risk of endometrioid or clear cell epithelial
ovarian tumours (odds ratio (OR) 2.56; 95% confidence interval (CI) 1.32-4.
94). In addition, the risk associated with oestrogen replacement therapy wa
s much larger in women with an intact genital tract (OR 3.00; 95% CI 1.54-5
.85) than in those with a history of either hysterectomy or tubal ligation.
Post-menopausal oestrogen replacement therapy may, therefore, be a risk fa
ctor associated with endometrioid and clear cell tumours in particular. Add
itionally, the risk may be increased predominantly in women with an intact
genital tract. These associations could reflect a possible role of endometr
iosis in the development of endometrioid or clear cell ovarian tumours. (C)
1999 Cancer Research Campaign.