Literature DB >> 8845586

Estrogen replacement therapy in survivors of breast cancer: a risk-benefit assessment.

J A Eden1.   

Abstract

The use of hormone replacement therapy (HRT) after breast cancer is controversial. For a minority of such women, menopausal symptoms such as hot flushes can be so severe as to compromise quality of life. Moderate doses of progestogens alone are an effective therapy for hot flushes in around two-thirds of patients and poorly absorbed topical estrogens are well tolerated and effective for vaginal dryness. However, for a small number of women, the only effective therapy for hot flushes is estrogen replacement. Women with early stage breast cancer are unlikely to die from this disease and will be more likely to be affected by age-related diseases such as heart disease, strokes and osteoporotic fractures. These women may also benefit from estrogen replacement. Prospective trials are currently under way to determine the safety of HRT after breast cancer.

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Year:  1996        PMID: 8845586     DOI: 10.2165/00002512-199608020-00006

Source DB:  PubMed          Journal:  Drugs Aging        ISSN: 1170-229X            Impact factor:   3.923


  26 in total

1.  Combined oestrogen-progestogen replacement and breast cancer risk.

Authors:  I Persson; J Yuen; L Bergkvist; H O Adami; R Hoover; C Schairer
Journal:  Lancet       Date:  1992-10-24       Impact factor: 79.321

Review 2.  Hormone therapy to prevent disease and prolong life in postmenopausal women.

Authors:  D Grady; S M Rubin; D B Petitti; C S Fox; D Black; B Ettinger; V L Ernster; S R Cummings
Journal:  Ann Intern Med       Date:  1992-12-15       Impact factor: 25.391

Review 3.  Progestin regulation of cellular proliferation.

Authors:  C L Clarke; R L Sutherland
Journal:  Endocr Rev       Date:  1990-05       Impact factor: 19.871

4.  A meta-analysis of the effect of estrogen replacement therapy on the risk of breast cancer.

Authors:  K K Steinberg; S B Thacker; S J Smith; D F Stroup; M M Zack; W D Flanders; R L Berkelman
Journal:  JAMA       Date:  1991-04-17       Impact factor: 56.272

5.  Progestins both stimulate and inhibit breast cancer cell cycle progression while increasing expression of transforming growth factor alpha, epidermal growth factor receptor, c-fos, and c-myc genes.

Authors:  E A Musgrove; C S Lee; R L Sutherland
Journal:  Mol Cell Biol       Date:  1991-10       Impact factor: 4.272

6.  Oestrogen therapy after the menopause--boon or bane?

Authors:  B K Armstrong
Journal:  Med J Aust       Date:  1988-03-07       Impact factor: 7.738

7.  Relative risks and benefits of long-term estrogen replacement therapy: a decision analysis.

Authors:  R D Gorsky; J P Koplan; H B Peterson; S B Thacker
Journal:  Obstet Gynecol       Date:  1994-02       Impact factor: 7.661

8.  Long-term adjuvant tamoxifen in early breast cancer: effect on bone mineral density in postmenopausal women.

Authors:  T Fornander; L E Rutqvist; H E Sjöberg; L Blomqvist; A Mattsson; U Glas
Journal:  J Clin Oncol       Date:  1990-06       Impact factor: 44.544

9.  Fatal myocardial infarction in the Scottish adjuvant tamoxifen trial. The Scottish Breast Cancer Committee.

Authors:  C C McDonald; H J Stewart
Journal:  BMJ       Date:  1991-08-24

10.  A link between breast cancer and local estrogen biosynthesis suggested by quantification of breast adipose tissue aromatase cytochrome P450 transcripts using competitive polymerase chain reaction after reverse transcription.

Authors:  S E Bulun; T M Price; J Aitken; M S Mahendroo; E R Simpson
Journal:  J Clin Endocrinol Metab       Date:  1993-12       Impact factor: 5.958

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  1 in total

Review 1.  Clodronate: a review of its use in breast cancer.

Authors:  M Hurst; S Noble
Journal:  Drugs Aging       Date:  1999-08       Impact factor: 3.923

  1 in total

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