Tamoxifen and breast cancer risk in women harboring a BRCA1 germline mutation: computed efficacy, effectiveness and impact

Citation
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
Citations number
36
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF ONCOLOGY
ISSN journal
10196439 → ACNP
Volume
18
Issue
1
Year of publication
2001
Pages
5 - 10
Database
ISI
SICI code
1019-6439(200101)18:1<5:TABCRI>2.0.ZU;2-6
Abstract
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.