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Drugs| Volume 9, ISSUE 4, P229-234, December 1999

Selective oestrogen receptor modulators

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      Abstract

      The relevance of hormone-replacement therapy (HRT) in the treatment of the short- and long-term complications of the menopause has become clearly evident. This treatment, however, has been associated with the emergence of complications, namely breast cancer and endometrial neoplasia.
      These side effects have led to research in the direction of tissue-specific effects leading to the evolution of selective oestrogen receptor modulators (SERMs). Tamoxifen was the first SERM employed in the prevention of breast cancer recurrence. Although anti-oestrogenic to the breast tissue, tamoxifen was found to maintain bone mass and preserve a favourable lipoprotein profile. Tamoxifen, however, led to endometrial stimulation with consequent polyp formation and hyperplasia.
      Raloxifene, a more recent SERM appears to have similar effects as tamoxifen on breast tissue, bone density and the lipoprotein profile. However, unlike tamoxifen, raloxifene does not appear to stimulate the endometrium – on the contrary it appears to be anti-oestrogenic to the endometrial epithelium. A more recent SERM, droloxifene appears to have a more anti-oestrogenic effect to the endometrium with bone sparing effects.
      Raloxifene has not been shown to improve on the short-term effects of the menopause, such as hot flushes and sweats. Similar to HRT, there appears to be a slight risk for deep vein thrombosis with raloxifene treatment.
      Tibolone is a SERM-like compound with beneficial effects on both the short- and the long-term complications of the menopause. Tibolone appears to have a beneficial influence of hot flushes, bone density and the lipoprotein profile. Conversely, tibolone does not appear to stimulate significantly either breast or endometrial tissue.
      SERMS and SERM-like compounds appear to have a promising future for the treatment and prevention of menopausal complications. Clinical proof for the affectiveness is still required. Possibly with further pharmacological manipulation more modern SERMS may be able to reduce both the short- and long-term complications of the menopause and simultaneously reduce the incidence of neoplasia such as breast and uterine carcinoma.
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      References

      REFERENCES

        • Diczfalusy E.
        • Fraser I.
        The discovery of reproduction steroid hormone and recognition of the physiological role.
        in: Fraser I. Jansen R. Lobo R. Whitehead M. Oestrogens & Progesterone in Clinical Practice. Churchill Livingstone,, London1998: 3-11
        • Baum M.
        Tamoxifen-Treatment of choice, why look for alternatives.
        British Journal Cancer. 1998; 78: 124-127
        • Delmas F.D.
        • Bjarnason N.H.
        • Mitlak B.H.
        Effects of raloxifene on bone mineral density, serum cholesterol concentrations and uterine endometrium in postmenopausal women.
        NEJM. 1997; 337: 1641-1647
        • Bryant Hu
        • Dere W.H.
        Selective estrogen receptor modulators. An alternative to hormone replacement therapy.
        Proc Soc Exp Biol Med. 1998; 217(1): 45-52
        • Henderson V.W.
        • Hill P.
        Estrogen & Alzheimer’s disease.
        in: Asch R. Studd J. Progress in Reported Medicine. Parthenon Publishing,, New York,1995: 185-193
        • Ravnikar V.A.
        Compliance with hormone replacement therapy.
        Are women receiving the full impact of hormone replacement therapy’s preventative health benefits. Women’s health issues. 1992; 2: 75-82
        • Brincat M.
        • Galea R.
        • Baron Y.M.
        • Xuereb A.
        Changes in bone collagen markers and in bone density in hormone treated and untreated postmenopausal women.
        Maturitas. 1997; 2: 171-177
        • Gambrell R.
        • Teran A.
        Changes in lipids and lipoproteins with long term estrogen deficiency and hormone replacement therapy.
        Am J Obstet Gynaecol. 1999; 165: 307-315
        • Panay N.
        • Studd J.
        Progesterone intolerance and compliance with hormone replacement therapy in menopausal women.
        Hum Reprod Update. 1997; 2: 159-171
        • Whitecroft S.
        • Crook D.
        • Marsh M.
        Long term effects of oral and transdermal hormone replacement therapy on serum lipids and lipoprotein concentrations.
        Obstet Gynaecol. 1994; 84: 1-5
        • Farrish E.
        • Fletcher C.
        • Hart D.
        Lipoproteins and apoprotein levels in postmenopausal women during treatment with norethisterone.
        Clin Chem Acta. 1996; 159: 147-151
        • Psaty B.M.
        • Heckbert S.R.
        • Atkins D.
        The risk of myocardial infarction associated with the combined use of estrogens and progestins in postmenopausal women.
        Arch Intern Med. 1994; 154(2): 1333-1339
        • Nabulsi A.
        • Folsom A.
        • White A.
        Association of hormone replacement therapy with various cardiovascular risk factors in postmenopausal women.
        NEJM. 1993; 328: 1069-1075
      1. Lancet. 1997; 350: 1047-1059
        • Sillero Arenas M.
        • Delgado Rodriguez M.
        • Rodigues Canteras R.
        • Bueno Cavanillas A.
        • Galvez Vargas R.
        Menopausal hormone replacement therapy and breast cancer: a meta-analysis.
        Obstet Gynecol. 1992; 79(2): 286-294
        • Kedar R.P.
        • Bourne T.H.
        • Powles T.J.
        Effects of tamoxifen on uterus and ovaries of postmenopausal women in a randomised breast cancer prevention trial.
        Lancet. 1994; 343: 1321-1328
        • Naeven P.
        • Muylder X.
        • Van Belle Y.
        • Vanderlick G.
        • De Muylder E.
        Hysteroscopic follow up during tamoxifen treatments.
        Eur J Obstet Gynaecol Reprod Biol. 1990; 35: 235-238
        • Fuchs Young R.
        • Glase Brrok A.L.
        Raloxifene is a tissue agonist/antagonist that functions through the estrogen receptor.
        Ann NY Acad Sci. 1995; 761: 355-360
        • Cummings S.R.
        • Eckert S.
        • Krueger K.A.
        The effect of raloxifene on risk of breast cancer in postmenopausal women: results from the MORE randomized trial, Multiple Outcomes of Raloxifene Evaluation.
        JAMA. 1999; 28(23): 2189-2197
        • Christiansen C.
        • Christiansen M.S.
        • Transbul I.
        Bone mass in postmenopausal women after withdrawal of oestrogen/gestagen replacement therapy.
        Lancet. 1981; 1: 459-461
        • Love R.
        • Mazess R.
        • Bardenh H.S.
        Effects of tamoxifen on bone mineral density in postmenopausal women with breast cancer.
        N Engl J Med. 1992; 326(1): 852-856
        • Grey A.
        • Stapleton J.
        • Evans M.
        • Tatnell M.
        • Ames R.
        • Reid E.
        The effect of the antioestrogen tamoxifen on bone mineral density in normal late postmenopausal women.
        JAMA. 1995; 99: 636-641
        • Turken S.
        • Siris E.
        • Seldin D.
        • Flaster E.
        • Hyman G.
        • Lindsay R.
        Effects of tamoxifen on spinal bone density in women with breast cancer.
        J Nat Cancer Inst. 1989; 81: 1086-1088
        • Powles T.
        • Hickish T.
        • Kanis J.
        • Tidy A.
        • Ashley S.
        Effect of Tamoxifen on bone mineral density measured by dual-energy X-ray absorptiometry in healthy pre-menopausal and postmenopausal women.
        J Clin Oncol. 1996; 14: 78-84
        • Ke H.
        • Chen H.
        • Qi H.
        Effects of droloxifene on prevention of cancellous bone loss and bone turnover in the axial skeleton of aged, ovariectomised rats.
        Bone. 1995; 17: 491-496
        • Chen H.
        • Ke H.
        • Jee W.
        Droloxifene prevents ovariectomy induced bone loss in tibia and femora of aged female rats.
        A dual energy X-ray absorptiometric and histomorphometric study. J Bone Miner Res. 1995; 10: 1256-1262
        • Grasser W.
        • Pan L.
        • Thompson D.
        • Paralkar V.
        Common mechanism for the estrogen agonist and antagonist activities of droloxifene.
        J Cell Biol. 1997; 65: 159-171
        • McDonald C.C.
        • Stewart H.J.
        Fatal mycocardial infarction in the Scottish adjuvant tamoxifen trial.
        Br Med J. 1991; 303: 435-437
      2. Rutguist, L. E. Mattsson, A. 1993, Cardiac and thromboembolic morbidity amongst postmenopausal women with early-stage breast cancer in a randomised trial of adjuvant tamoxifen, J National Cancer Institute, 1993, 85, 1398, 1406

        • Rymer J.
        • Crook D.
        • Sidhu M.
        • Chapman M.
        • Stevenson J.C.
        Effects of tibolone on serum concentrations of lipoprotein(a) in postmenopausal women.
        Acta Endocrinol. 1993; 128(3): 259-262
        • Stevenson J.C.
        • Crook D.
        • Godsland I.F.
        • Collins P.
        • Whitehead M.I.
        Hormone replacement therapy and the cardiovascular system. Non lipid effects.
        Drugs. 1994; 47(suppl 2): 35-41
        • Clarkson T.B.
        • Anthony M.S.
        • Jerome C.P.
        Lack of effect of raloxifene on coronary artery atherosclerosis of postmenopausal monkeys.
        J Clin Endocrinol Metab. 1998; 83: 721-726
        • Fisher B.
        • Redrono C.
        Systemic therapy in mode-negative patients. Updated findings from NSABP clinical trials.
        J Nat Cancer Inst Monogr. 1990; : 105-116
        • Veronesi U.
        • Mainsonneuve P.
        • Costa A.
        Prevention of breast cancer with tamoxifen: Preliminary findings from the Italian randomized trial among hysterectomised women.
        Lancet. 1998; 352: 98-101
        • Powles T.
        • Eeles R.
        • Ashley S.
        Interim analysis of the incidence of breast cancer in the Royal Marsden Hospital tamoxifen randomised chemoprevention trial.
        Lancet. 1998; 352: 98-101
        • Butterweck A.
        • Brincat M.
        • Galea R.
        The effect of an extract of a phyeophycac alga (EPP) on human breast carcinoma cells related to tamoxifen and oestradiol.
        Poster presentation at the Meeting of the Menopause Society, Edinburgh,. 1998;
        • Pagannini-Hill A.
        • Henderson V.W.
        Estrogen deficiency and risk of Alzheimer’s disease in women.
        Am J Epidemiology. 1994; 140: 256-261
      3. Hallstrom, T. Mental disorder and sexuality in the climacteric. A study in psychiatric epidemiology. Scandinavian University Books, Gothenburg, Sweden, 1973

        • Bangay G.T.
        • Vassey M.P.
        • McPherson C.
        Study of symptoms in middle life with special reference to the menopause.
        Br Med J. 1980; 281: 181-183
        • Fillit H.
        • Weinrub H.
        • Cholst I.
        • Lume V.
        • McEwan B.
        • Amador R.
        • Zabriskie J.
        Observations in a preliminary open trial of estradiol therapy for senile dementia.
        Alzheimer’s type. Psychoneuroendocrinology. 1986; 11: 337-345
        • Honjo H.
        • Ogenio Y.
        • Naltoh K.
        In vivo effects by estrone sulphate on the central nervous system – senile dementia (Alzheimer’s type).
        Journal of steroid biochemistry. 1989; 34: 521-525
        • Crook D.
        Effects of estrogens and progestogens on plasma lipids and lipoproteins.
        in: Fraser I. Jansen R.P.S. Lobo R.A. Whitehead A.I. Estrogens and progestogens in clinical pratice. (Churchill Livingstone),, New York1998: 787-798
        • Lindsay P.C.
        • Shaw R.W.
        • Bennink H.J.
        • Kicovic P.
        The effect of add-back treatment with tibolone (livial) on patients treated with the gonadotropin-releasing hormone agonist triptorelin (decapeptyl).
        Fertil Steril. 1996; 65(2): 342-348
        • Lippuner K.
        • Haenggi W.
        • Birkaeuser M.H.
        • Casez J.P.
        • Jaeger P.
        Prevention of postmenopausal bone loss using tibolone or conventional peroral or transdermal hormone replacement therapy with 17 beta-estradiol and dydrogesterone.
        J Bone Miner Res. 1997; 12(5): 806-812
        • Zanberg P.
        • Peter J.
        • Demarcker P.
        • Smit M.
        • de Reeder F.
        • Meuleman D.
        Tibolone prevents atherosclerotic lesion formation in cholesterol fed, ovariectomised rats.
        Arteriosclero Thromb Vasc Biol. 1998; 18: 1844-1854
        • Beardsworth S.A.
        • Kearney C.E.
        • Purdie D.W.
        Prevention of postmenopausal bone loss at lumbar spine and upper femur with tibolone: a two year randomised controlled trial.
        Br J Obstet Gynaecol. 1999; 106(7): 678-683
        • Kloosterboer H.J.
        • Deckers G.I.I.
        • de Gooyer M.E.
        • Dijkema R.
        • Orlemans F.O.
        • Schoonen W.G.
        Pharmacological properties of a new selective antiprogestagen: Org 33628.
        Ann N Y Acad Sci. 1995; 761: 192-201