Selective estrogen receptor modulators and breast câncer risk reduction: tamoxifen and raloxifene

Authors

  • Juliana Oliveira Divisão Médica Eli Lilly do Brasil, São Paulo-SP.
  • Oswaldo Luís Bracco Divisão Médica Eli Lilly do Brasil, São Paulo-SP.
  • Márcia Jehá Kayath Divisão Médica Eli Lilly do Brasil, São Paulo-SP.
  • Ezio Novais Presidente da Sociedade Brasileira de Mastologia (sbm); Serviço de Ginecologia e Mastologia do Hospital São Rafael, Salvador-BA.
  • Almir Urbanetz Ambulatório de Climatério do Serviço de Ginecologia da Universidade Federal do Paraná (ufpr), curitiba-PR
  • Maurício Magalhães Costa Setor de Ginecologia Oncológica do Hospital Universitário clementino Fraga Filho/Universidade Federal do Rio de laneiro (HUCFF/UFRi), Rio de |aneiro-R|.

Keywords:

Raloxifene, Breast câncer, SERM

Abstract

Serms (selective estrogen receptor modulators) are agents that blnd to estrogen receptors
and act as estrogen agonlsts In some tissues (bone), and as estrogen antagonists In other
tissues (uterus and breast). Because they act as estrogen-receptors In breast, SERMs have
shown to be effectlve in reducing the risk of breast câncer. The use of tamoxifen in breast
câncer prevention was evaluated in four major clinicai trials and it has been demonstrated that
tamoxifen, used for 5 years, significantly decreases the incidence of breast câncer in high-risk women. The increase in the incidence ofendometrial câncer makes it important to select correctly
the patients who will benefit from tamoxifen therapy. Raloxifene is a second-generation SERM
that binds to estrogen receptors with high affinity. It has estrogen antagonistic activity on the
breast and uterus, and estrogen-like activity on bone. In the More study, the main clinicai trial
done using raloxifeno, a significant reduction in the relative risk of breast câncer of 76% was
demonstrated, in postmenopausal women with osteoporosis, after three years of follow-up.
These results were confirmed after four years of follow-up. The breast câncer risk reduction with raloxifene supports a new perspective in reducing the risk of breast câncer and optimize women's health.

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References

1.ABE O, ABE R, ENOMOTO K et al.

Tamoxifen for early breast câncer:

an overview of the randomised

trials. Early Breast Câncer Trialists'

Collaborative Group. Lancet 1998; 351:

1451-67.

2.BEATSON 6T. On the treatment of

inoperable cases of the carcinoma of

the mamma: suggestions for a new method of treatment with illustrative

cases. Lancet 1896; ii: 104-7.

3.BENTREM DJ, CRAIG J. Tamoxifen,

raloxifene and the prevention of breast

câncer. Minerva Endocrinol 2002; 27:

127-39.

4.BOYD NF, DITE GS, STONE J et al. Heritability of mammographic density,

a risk factor for breast câncer. N Engl J Med 2002; 347: 886-94.

5.CAULEY J, LUCAS FL, KULLER LH et

al. Elevated serum estradiol and

testosterone concentrations are

associated with a high risk for breast

câncer. Ann Intern Med 1999; 130:

270-7.

6.CAULEY J, NORTON L, LIPPMAN M et al. Continued breast câncer risk reduction

in postmenopausal women treated

with raloxifene: four-year results from

the More trial. Breast Câncer Res Treat

2001; 65: 125-34.

7.CUMMINGS SR, ECKERT S, KRUEGER KA. The effect of raloxifene on risk of breast

câncer in postmenopausal women:

results from the More randomized trial.

JAMA 1999; 281: 2189-97.

8.DALTON RR, KALLAB AM. Chemoprevention

of breast câncer. South Med J 2001; 94:

7-15.

9.DELMAS PD, ENSRUD KE, ADACHIJD et

al. Efficacy of raloxifene on vertebral

fracture risk reduction in postmenopausal women with osteoporosis: four-year

results from a randomized clinicai trial.

J Clin Endocrinol Metab 2002; 87:

3609-17.

10.DELMAS PD, GENANT HK, CRANS GG

et al. Severity of prevalent vertebral

fractures and the risk of subsequent

vertebral and nonvertebral fractures:

results from the More trial. Bone 2003;

33: 522-32.

11.DUNN BK, FORD L. From adjuvant

therapy to breast câncer prevention: BCPT and Star. Breast J 2001; 7:

144-57.

12.FISHER B, CONSTANTINOJP, WICKERHAM

DL et al. Tamoxifen for prevention of

breast câncer: report of the National

Surgical Adjuvant Breast and Bowel

Project: P-l study. J Natl Câncer Inst

1998; 90: 1371-88.

13.GOTTARDIS MM, JORDAN C. Antitumor

actions of keoxifeno and tamoxifen in

the N-nitrosimethylurea-induced rat mammary câncer model. Câncer Res

1987; 48: 4020-4.

14.JACKSON VP, SAN MARTIN J, SECREST RJ et al. Comparison of the effect of

raloxifene and continuous-combined

hormone therapy on mammographic

breast density and breast tenderness

in postmenopausal women. Am J Obstet Gynecol 2003; 188: 389-94.

15.JOLLY EE, BJARNASON NH, NEVEN P. Prevention of osteoporosis and uterine

effects in postmenopausal women taking

raloxifene for five years. Menopause

2003; 10: 337-44.

16.LACASSAGNE A. Hormonal pathogenesis

of adenocarcinoma of the breast. Am J Câncer 1935; 27: 217-25.

17.LIPPMAN ME, BOLAN G. Oestrogenresponsive human breast câncer in

long-term tissue culture. Nature 1975;

256: 592-3.

18.MARICIC M, ADACHI JD, SARKAR S, WU W, WONG M, HARPER KD. Early

effects of raloxifene on clinicai

vertebral fractures at twelve months

in postmenopausal women with

osteoporosis. Arch Intern Med 2002;

162: 1140-3.19.OSBORNE CK. Stèroid hormone

receptors in breast câncer management.

Breast Câncer Res Treat 1998; 51:

227-38.

20.PARK W-C, JORDAN C. Selective estrogen

receptor modulators (Serms) and their

roles in breast câncer prevention. Trends Mol Med 2002; 8: 82-8.

21.PRITCHARD K. Breast câncer prevention with selective estrogen receptor

modulators: a perspective. Ann N Y

Acad Sei 2001; 949: 89-98.

22.SMITH RE, GOOD BC. Chemoprevention

of breast câncer and the trials of the

National Surgical Adjuvant Breast and

Bowel Project and others. Endocr Relat

Câncer 2003; 10: 347-57.

23.STRASSER-WEIPPL K, GOSS PE.

Prevention of breast câncer using Serms

and aromatase inhibitors. Journal of Mammary Gland Biology and Neoplasia

2003; 8: 5-18.

24.VERONESI U, MAISONNEUVE P, COSTA

A et al. Prevention of breast câncer

with tamoxifen: preliminary findings

from the italian randomised trial among

hysterectomised women. Lancet 1998;

352: 93-7.

Published

2026-07-29

How to Cite

Oliveira, J., Bracco, O. L., Kayath, M. J., Novais, E., Urbanetz, A., & Costa, M. M. (2026). Selective estrogen receptor modulators and breast câncer risk reduction: tamoxifen and raloxifene. Mastology, 14(1). Retrieved from https://mastology.org/journal/article/view/2106

Issue

Section

Review Articles