Breast cancer is the most common cancer in women in the Westernworld. Because breast cancer is estrogen-dependent, reducingestrogen secretion by oophorectomy, hypophysectomy, or adrenalectomycan cause the cancer to regress. The need for these surgicalprocedures was reduced by the introduction of tamoxifen, whichacts as an antiestrogen by inhibiting the binding of estrogento estrogen receptors. Tamoxifen was approved by the Food andDrug Administration in 1977 for the treatment of women withadvanced breast cancer and several years later for adjuvanttreatment of primary breast cancer.1
Benefits in Women with and Women without Metastases to the Axillary Lymph Nodes
Benefits in Elderly Women
Tamoxifen in Combination with Adjuvant Chemotherapy
Treatment of Metastatic Breast Cancer
Treatment of Men with Breast Cancer
Resistance
Ancillary Benefits
Serum Lipoproteins and Mortality from Cardiovascular Causes
Changes in Bone Mineral Density
Prevention of Contralateral Breast Cancer and of Breast Cancer in Women at High Risk
Toxicity
Menopausal Symptoms
Ocular, Thromboembolic, and Hematologic Effects
Endometrial Cancer
Conclusions
Source Information
From the Department of Medicine, Division of Medical Oncology, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Dr., San Antonio, TX 78284-7884, where reprint requests should be addressed to Dr. Osborne.
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Weatherman, R. V., Chang, C.-Y., Clegg, N. J., Carroll, D. C., Day, R. N., Baxter, J. D., McDonnell, D. P., Scanlan, T. S., Schaufele, F.
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McDonnell, D. P., Connor, C. E., Wijayaratne, A., Chang, C.-y., Norris, J. D.
(2002). Definition of the Molecular and Cellular Mechanisms Underlying the Tissue-selective Agonist/Antagonist Activities of Selective Estrogen Receptor Modulators. Recent Prog Horm Res
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Dardes, R. C., Bentrem, D., O'Regan, R. M., Schafer, J. M., Jordan, V. C.
(2001). Effects of the New Selective Estrogen Receptor Modulator LY353381.HCl (Arzoxifene) on Human Endometrial Cancer Growth in Athymic Mice. Clin. Cancer Res.
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Jordan, V. C., Gapstur, S., Morrow, M.
(2001). Selective Estrogen Receptor Modulation and Reduction in Risk of Breast Cancer, Osteoporosis, and Coronary Heart Disease. JNCI J Natl Cancer Inst
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Greenberger, L. M., Annable, T., Collins, K. I., Komm, B. S., Lyttle, C. R., Miller, C. P., Satyaswaroop, P. G., Zhang, Y., Frost, P.
(2001). A New Antiestrogen, 2-(4-Hydroxy-phenyl)-3-methyl-1-[4-(2-piperidin-1-yl-ethoxy)-benzyl]-1H-indol-5-ol hydrochloride (ERA-923), Inhibits the Growth of Tamoxifen-sensitive and -resistant Tumors and Is Devoid of Uterotropic Effects in Mice and Rats. Clin. Cancer Res.
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Robertson, J. F., Nicholson, R. I., Bundred, N. J., Anderson, E., Rayter, Z., Dowsett, M., Fox, J. N., Gee, J. M. W., Webster, A., Wakeling, A. E., Morris, C., Dixon, M.
(2001). Comparison of the Short-Term Biological Effects of 7{alpha}-[9-(4,4,5,5,5-pentafluoropentylsulfinyl)-nonyl]estra-1,3,5, (10)-triene-3,17{beta}-diol (Faslodex) versus Tamoxifen in Postmenopausal Women with Primary Breast Cancer. Cancer Res.
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Fong, K., Kung, R., Lytwyn, A., Trudeau, M., Chapman, W., Nugent, P., Glanc, P., Manchul, L., Szabunio, D., Myhr, T.
(2001). Endometrial Evaluation with Transvaginal US and Hysterosonography in Asymptomatic Postmenopausal Women with Breast Cancer Receiving Tamoxifen. Radiology
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Hann, L. E., Gretz, E. M., Bach, A. M., Francis, S. M.
(2001). Sonohysterography for Evaluation of the Endometrium in Women Treated with Tamoxifen. Am. J. Roentgenol.
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Schafer, J. M., Lee, E.-S., Dardes, R. C., Bentrem, D., O'Regan, R. M., De Los Reyes, A., Jordan, V. C.
(2001). Analysis of Cross-Resistance of the Selective Estrogen Receptor Modulators Arzoxifene (LY353381) and LY117018 in Tamoxifen-stimulated Breast Cancer Xenografts. Clin. Cancer Res.
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