Mc. Pike et al., A HORMONAL CONTRACEPTIVE APPROACH TO REDUCING BREAST AND OVARIAN-CANCER RISK - AN UPDATE, Endocrine-related cancer, 4(1), 1997, pp. 125-133
Epidemiological studies have consistently found that bilateral oophore
ctomy at a young age substantially reduces breast cancer risk. Such su
rgical menopause around age 35 has been found to reduce risk by 60 to
75%. A reversible medical oophorectomy using an agent such as a gonado
tropin-releasing hormone agonist (GnRHA) should achieve a similar redu
ction in risk. Although the use of GnRHA alone is unacceptable because
of the associated hypoestrogenic side-effects, these can be satisfact
orily prevented by add-back low-dose estrogen treatment with intermitt
ent progestin to protect the endometrium. It is estimated that a regim
en of GnRHA plus add-back ultra low-dose estrogen and progestin would
prevent some two-thirds of current breast cancer if used from age 30.
If used from age 20 almost nine out of ten current breast cancer cases
would be avoided. If, as is likely, these estimates also apply to wom
en at high genetic risk of breast cancer because of possession of a BR
CA1 or BRCA2 gene, their breast cancer risk would be reduced to below
that of 'normal' women. The protective effects on ovarian cancer are c
alculated to be greater than the protective effects on breast cancer.
Practical chemoprevention of breast and ovarian cancer using this appr
oach should be possible within 5 years.