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Effects of Raloxifene Combined with Low-dose Conjugated Estrogen on the Endometrium in Menopausal Women at High Risk for Breast Cancer
Author(s) -
Andrea Lúcia Bastos Carneiro,
Ana Paula Curi Spadella,
Fabiola Souza,
Karen Borelli Ferreira Alves,
Joaquim Teodoro de Araujo-Neto,
Mauro Abi Haidar,
Rita de Cássia de Maio Dardes
Publication year - 2021
Publication title -
clinics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.618
H-Index - 61
eISSN - 1980-5322
pISSN - 1807-5932
DOI - 10.6061/clinics/2021/e2380
Subject(s) - raloxifene , medicine , endometrium , endometrial cancer , gynecology , endometrial biopsy , urology , selective estrogen receptor modulator , atypia , breast cancer , menopause , estrogen , endometrial polyp , cancer , tamoxifen , pathology
OBJECTIVES: To compare the effects of low-dose conjugated estrogen (CE), raloxifene, and the combination thereof on the endometrium of postmenopausal women. METHODS: Postmenopausal women between 45 and 60 years of age, with Gail score≥1.67 and no endometrial disorders, were randomly assigned to receive low-dose CE (0.3 mg), raloxifene (60 mg), or combined therapy for 1 year. Transvaginal ultrasound was performed at baseline and every 3 months; the Kupperman Index was assessed at baseline and every 6 months. Endometrial biopsies were performed if endometrial thickness (ET) was ≥5 mm or if vaginal bleeding occurred. The primary outcome was the occurrence of ET≥5 mm over the one-year period. RESULTS: Seventy-three women were randomly assigned and analyzed on an intent-to-treat basis. Eight, three, and four women in the CE, raloxifene, and combination groups, respectively, exhibited ET≥5 mm. No genital bleeding was reported in the combination group. Endometrial biopsy revealed atrophy or polyps in all groups, with one patient in the CE group exhibiting a proliferative endometrium without atypia. At 6 months, there was a progressive increase in mean ET in the CE group, but not in the other two groups, with statistically significant differences at 6, 9, and 12 months. Mean scores for vasomotor symptoms and Kupperman Index favored the CE and combination groups over raloxifene. CONCLUSION: Combined raloxifene and low-dose CE decreased the severity of menopausal symptoms to a similar extent as CE alone and had similar effects as raloxifene alone on the endometrium.

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