J 2011

Oral contraceptives and risk of ovarian and breast cancers in BRCA mutation carriers: a meta-analysis

CIBULA, David; Michal ZIKÁN; Ladislav DUŠEK and Ondřej MÁJEK

Basic information

Original name

Oral contraceptives and risk of ovarian and breast cancers in BRCA mutation carriers: a meta-analysis

Authors

CIBULA, David (203 Czech Republic, guarantor); Michal ZIKÁN (203 Czech Republic); Ladislav DUŠEK (203 Czech Republic, belonging to the institution) and Ondřej MÁJEK (203 Czech Republic, belonging to the institution)

Edition

Expert Review of Anticancer Therapy, 2011, 1473-7140

Other information

Language

English

Type of outcome

Article in a journal

Field of Study

30200 3.2 Clinical medicine

Country of publisher

United Kingdom of Great Britain and Northern Ireland

Confidentiality degree

is not subject to a state or trade secret

Impact factor

Impact factor: 2.652

RIV identification code

RIV/00216224:14110/11:00053296

Organization unit

Faculty of Medicine

UT WoS

000294978600012

Keywords in English

breast cancer; BRCA1; BRCA2; combined oral contraceptives; ovarian cancer

Tags

International impact, Reviewed
Changed: 27/6/2012 17:14, RNDr. Ondřej Májek, Ph.D.

Abstract

V originále

Prophylactic salpingo-oophorectomy is currently the only effective strategy available for decreasing ovarian cancer risk in BRCA1/2 mutation carriers. Significantly decreased risk of ovarian cancer associated with the use of combined oral contraceptives (COCs) was shown in the general population, which could be an alternative approach for those who do not accept risk-reducing surgery. Cohort, case–control and case–case studies published in English up to December 2009 reporting the association of ovarian or breast cancer risk with the use of COCs and presenting BRCA status were selected for meta-analysis. Meta-analysis of three case–control studies showed a significant risk reduction of ovarian cancer in BRCA1/2 mutation carriers who were associated with any past COC use and significant trend by duration of COC use (OR: 0.95; 95% CI: 0.93–0.97). No significant increase in breast cancer risk associated with COC use has been found in case–control studies in BRCA1 (OR: 1.08; p = 0.250), in BRCA2 (OR: 1.03; p = 0.788) mutation carriers or in case–case studies in BRCA1/2 carriers (OR: 0.80; p = 0.147). Significantly increased risk of breast cancer was only shown on a subset of cohort studies in BRCA1 mutation carriers (OR: 1.48; 95% CI: 1.14–1.92). In conclusion, meta-analysis confirmed significantly decreased ovarian cancer risk in BRCA1/2 mutation carriers associated with the use of COCs comparable to the relative extent shown in the general population. Data on the risk of breast cancer associated with COC use in BRCA mutation carriers are heterogeneous and results are inconsistent. COCs can be considered as an alternative strategy in the chemoprevention of ovarian cancer in BRCA1 mutation carriers who do not accept prophylactic salpingo-oophorectomy above the age of 30 years.