Oral contraceptives and risk of breast cancer and ovarian cancer in women with a BRCA1 or BRCA2 mutation: A meta-analysis of observational studies

Author:

Park Junli12,Huang Dan34,Chang Yoon Jung356,Lim Myong Cheol578,Myung Seung-Kwon6910ORCID

Affiliation:

1. Center for Cancer Prevention and Detection, Hospital, National Cancer Center, Goyang, Korea

2. Department of Family Medicine, Myongji Hospital, Goyang, Korea

3. Division of Cancer Control & Policy, National Cancer Control Institute, National Cancer Center, Goyang, Korea

4. Department of Preventive Medicine, Seoul National University College of Medicine, Seoul, Korea

5. Department of Cancer Control and Population Health, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, Korea

6. Department of Family Medicine, Hospital, National Cancer Center, Goyang, Korea

7. Center for Gynecologic Cancer, Hospital, National Cancer Center, Goyang, Korea

8. Division of Tumor Immunology, Research Institute, National Cancer Center, Goyang, Korea

9. Department of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, Korea

10. Division of Cancer Epidemiology and Management, Research Institute, National Cancer Center, Goyang, Korea

Abstract

Abstract It remains inconclusive whether the use of oral contraceptives (OCs) alters the risks of breast or ovarian cancer in women with a BRCA1 or BRCA2 mutation. We investigated the association between OC use and the risks of breast or ovarian cancer in this group by using a meta-analysis. PubMed and EMBASE were searched using keywords until February 2021 to identify relevant studies that evaluated the association between OC ever use and the risks of breast or ovarian cancer in women with a BRCA1 or BRCA2 mutation. Twelve studies for breast cancer and eight studies for ovarian cancer were identified. In the random-effects meta-analysis, the ever use of OCs was significantly associated with an increased risk of breast cancer [odds ratio (OR), relative risk (RR), or hazard ration (HR) = 1.24; 95% confidence interval (CI) 1.08 – 1.41] and a decreased risk of ovarian cancer (OR/RR/HR = 0.53, 95% CI 0.41 – 0.67). Consistent findings were observed, when BRCA1 and BRCA2 mutation carriers were analyzed separately. The increased risk of breast cancer was observed only in the long-term (>5 years) users of OCs, while the decrease risk of ovarian cancer was observed regardless of the duration of OC use. The current study suggests that the ever use of OCs in BRCA mutation carriers is significantly associated with an increased risk of breast cancer and a decreased risk of ovarian cancer. Therefore, the use of OCs as chemoprevention of ovarian cancer should be cautious in BRCA mutation carriers.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,General Medicine

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