Kf. Mcgonigle et al., DEVELOPMENT OF ENDOMETRIAL CANCER IN WOMEN ON ESTROGEN AND PROGESTIN HORMONE REPLACEMENT THERAPY, Gynecologic oncology, 55(1), 1994, pp. 126-132
The presenting symptoms, hormonal regimens, treatment modalities, tumo
r pathology, and follow-up of 25 women developing endometrial cancer w
hile receiving postmenopausal estrogen and progestin therapy were inve
stigated retrospectively. Patients were interviewed and hormone therap
ies were confirmed through medical records. Pathology specimens were r
eviewed. Patients received conjugated estrogens (n = 20) or another es
trogen (n = 5). For those on conjugated estrogens, the mean daily dose
was 0.68 mg, monthly duration was 24.9 days, and monthly dose was 17.
0 mg. Women also received medroxyprogesterone acetate (n = 23) or nore
thindrone acetate (n = 2). The most common regimen was sequential medr
oxyprogesterone acetate, at a mean daily dose of 7.5 mg, monthly durat
ion of 9.3 days, and monthly dose of 68 mg (mean duration = 5.7 years)
. Most tumors were low stage and grade, with few demonstrating grade 3
disease (n = 2) or greater than 50% myometrial invasion (n = 2). Twen
ty-three (92%) had disease limited to the uterus, while two had stage
IIIA disease. All are alive and disease-free after a median follow-up
of 26 months. Estrogen and progestin therapy does not prevent endometr
ial cancer in all patients. Women who developed this tumor on sequenti
al therapy in general received less than the recommended guidelines fo
r daily dosage and monthly duration of progestin. Most patients had ea
rly-stage and low-grade disease. Continued vigilance in the care of wo
men on hormone replacement therapy is necessary even when combination
therapy is prescribed. (C) 1994 Academic Press, Inc.