F. Eisinger et al., Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation: computed efficacy, effectiveness and impact, INT J ONCOL, 18(1), 2001, pp. 5-10
The management of breast cancer prone women remains a tough issue despite t
he release of institutional guidelines. Currently, only the anti-estrogen a
gent Tamoxifen and prophylactic surgery are claimed to decrease breast canc
er incidence. However, efficacy of Tamoxifen, particularly in BRCA1 gene ca
rriers, remains controversial and acceptability of prophylactic surgery is
low. To evaluate the expected impact of Tamoxifen in preventing hereditary
breast cancers, a modelling was ma-de according to the efficacy of the trea
tment with respect to biological predictors of response: estrogen receptor
(ER) and pS2 status of a series of 33 BRCA1-related breast cancers (BRCA1-B
Cs), and using data on BRCA1-BCs penetrance, as well as compliance and acce
ptability of the strategy. Although, 88% of BRCA1-BCs are ER negative in ou
r series, 30% of cases are pS2 positive, implying a potential hormonal sens
itivity of a proportion of these cancers. From our modelling, the expected
impact of Tamoxifen in BRCA1 gene carriers is a reduction of breast cancer
incidence of about 10% according to acceptability and compliance, close to
that of 5% and of 13.5% for prophylactic mastectomy, according to acceptabi
lity rates from US and French surveys respectively. Since autonomy of choic
e is the root of Western ethics, cancer prone women should be informed abou
t the low but valuable expected reduction of incidence of breast cancer usi
ng Tamoxifen preventive therapy.