Literature DB >> 9741780

Tamoxifen--the treatment of choice. Why look for alternatives?

M Baum1.   

Abstract

Tamoxifen is currently established as the endocrine treatment of choice in breast cancer. In advanced breast cancer, response rates of up to 60% in women with oestrogen receptor (ER)-positive tumours have been reported. In early breast cancer, tamoxifen can produce significant benefits, both statistically and clinically, in terms of reduction in relative risk of relapse or death in all patient subgroups (i.e. ER status, aged < or > 50 years) except premenopausal women with ER-negative tumours. The major benefit, however, is seen in women over 50 years old with ER-positive tumours. The results of randomized trials suggest that the optimum duration of tamoxifen therapy is at least 5 years. Two large pragmatic trials (aTTom and ATLAS) are under way to determine whether additional benefit can be gained from continuing tamoxifen treatment beyond 5 years. Recent data also suggest possible synergism between tamoxifen and chemotherapy in the treatment of early breast cancer in post-menopausal women. Other benefits of tamoxifen treatment include reduction in the risk of developing contralateral breast cancer. Included among the non-breast cancer benefits of tamoxifen are reduced risk of cardiovascular disease and protection against bone loss in post-menopausal women. These benefits must be weighed against the possible increased incidence of endometrial cancer. Notwithstanding its undoubted success, there is a need for agents to improve upon tamoxifen. Newer agents, such as the luteinizing hormone-releasing hormone analogue goserelin and the new-generation aromatase inhibitors, such as anastrozole, will add new life to the search for an improved endocrine therapy for early breast cancer.

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Year:  1998        PMID: 9741780      PMCID: PMC2062753          DOI: 10.1038/bjc.1998.753

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  15 in total

1.  Long term effects of tamoxifen on blood lipid values in breast cancer.

Authors:  J A Dewar; J M Horobin; P E Preece; R Tavendale; H Tunstall-Pedoe; R A Wood
Journal:  BMJ       Date:  1992-07-25

2.  Five versus more than five years of tamoxifen therapy for breast cancer patients with negative lymph nodes and estrogen receptor-positive tumors.

Authors:  B Fisher; J Dignam; J Bryant; A DeCillis; D L Wickerham; N Wolmark; J Costantino; C Redmond; E R Fisher; D M Bowman; L Deschênes; N V Dimitrov; R G Margolese; A Robidoux; H Shibata; J Terz; A H Paterson; M I Feldman; W Farrar; J Evans; H L Lickley
Journal:  J Natl Cancer Inst       Date:  1996-11-06       Impact factor: 13.506

3.  A randomised study to compare the effect of the luteinising hormone releasing hormone (LHRH) analogue goserelin with or without tamoxifen in pre- and perimenopausal patients with advanced breast cancer.

Authors:  W Jonat; M Kaufmann; R W Blamey; A Howell; J P Collins; A Coates; W Eiermann; F Jänicke; B Njordenskold; J F Forbes
Journal:  Eur J Cancer       Date:  1995       Impact factor: 9.162

4.  Effects of tamoxifen on bone mineral density in postmenopausal women with breast cancer.

Authors:  R R Love; R B Mazess; H S Barden; S Epstein; P A Newcomb; V C Jordan; P P Carbone; D L DeMets
Journal:  N Engl J Med       Date:  1992-03-26       Impact factor: 91.245

Review 5.  Endocrine therapy for advanced breast cancer: a review.

Authors:  H B Muss
Journal:  Breast Cancer Res Treat       Date:  1992       Impact factor: 4.872

Review 6.  Tamoxifen-associated eye disease. A review.

Authors:  S G Nayfield; M B Gorin
Journal:  J Clin Oncol       Date:  1996-03       Impact factor: 44.544

7.  Changes in incidence of and mortality from breast cancer in England and Wales since introduction of screening. United Kingdom Association of Cancer Registries.

Authors:  M Quinn; E Allen
Journal:  BMJ       Date:  1995-11-25

8.  Effects of tamoxifen on cardiovascular risk factors in postmenopausal women after 5 years of treatment.

Authors:  R R Love; D A Wiebe; J M Feyzi; P A Newcomb; R J Chappell
Journal:  J Natl Cancer Inst       Date:  1994-10-19       Impact factor: 13.506

9.  Anastrozole, a potent and selective aromatase inhibitor, versus megestrol acetate in postmenopausal women with advanced breast cancer: results of overview analysis of two phase III trials. Arimidex Study Group.

Authors:  A Buzdar; W Jonat; A Howell; S E Jones; C Blomqvist; C L Vogel; W Eiermann; J M Wolter; M Azab; A Webster; P V Plourde
Journal:  J Clin Oncol       Date:  1996-07       Impact factor: 44.544

Review 10.  Use of tamoxifen for breast cancer: twenty-eight years later.

Authors:  I A Jaiyesimi; A U Buzdar; D A Decker; G N Hortobagyi
Journal:  J Clin Oncol       Date:  1995-02       Impact factor: 44.544

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  5 in total

1.  GAS6 is an estrogen-inducible gene in mammary epithelial cells.

Authors:  Rigen Mo; Yiwei Tony Zhu; Zhongyi Zhang; Sambasiva M Rao; Yi-Jun Zhu
Journal:  Biochem Biophys Res Commun       Date:  2006-12-11       Impact factor: 3.575

Review 2.  Comparative tolerability of first-generation selective estrogen receptor modulators in breast cancer treatment and prevention.

Authors:  M G Curtis
Journal:  Drug Saf       Date:  2001       Impact factor: 5.606

Review 3.  The value of adjuvant treatment in young women with breast cancer.

Authors:  Sally Clive; J Michael Dixon
Journal:  Drugs       Date:  2002       Impact factor: 9.546

4.  IGF status is altered by tamoxifen in patients with breast cancer.

Authors:  M J Campbell; J V Woodside; J Secker-Walker; A Titcomb; A J Leathem
Journal:  Mol Pathol       Date:  2001-10

5.  Tumorigenic effects of tamoxifen on the female genital tract.

Authors:  Kaei Nasu; Noriyuki Takai; Masakazu Nishida; Hisashi Narahara
Journal:  Clin Med Pathol       Date:  2008-03-01
  5 in total

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