Does the use of Oral Contraceptive Pills (OCPs) increase the risk of breast cancer?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: December 15, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Oral Contraceptive Pills and Breast Cancer Risk

Current or recent use of oral contraceptive pills (OCPs) is associated with a small increase in breast cancer risk (relative risk 1.2-1.6), but this risk disappears completely within 10 years of discontinuation, and the absolute risk remains very low in young women. 1

Magnitude and Timing of Risk

  • Current users have a relative risk of 1.24 (95% CI, 1.15-1.33) for breast cancer, though more recent analyses show a lower relative risk of 1.08 (95% CI, 1.00-1.17). 1

  • The elevated risk is confined to active hormonal exposure and resolves within 10 years after stopping OCPs, suggesting this is not a permanent carcinogenic effect. 1

  • Women using OCPs for more than 5 years show relative risks of 1.33-1.56, indicating a duration-dependent relationship. 2

  • The highest relative risk occurs in women under 34 years, but their baseline breast cancer incidence is so low that the absolute risk increase remains minimal. 1

Special Populations: Family History and BRCA Carriers

Women with a family history of breast cancer or BRCA1/2 mutations do not appear to have significantly amplified breast cancer risk from OCP use compared to women without such history. 1, 3

  • Meta-analyses show no significant association between OCP use and breast cancer risk in BRCA1/2 carriers overall. 2

  • One case-control study found modest increased risk in BRCA1 carriers (OR 1.20) with 5 or more years of use, particularly before age 40 (OR 1.38), while another found increased risk in BRCA2 carriers (OR 2.06). 2

  • Conversely, one study found low-dose OCPs decreased breast cancer risk in BRCA1 carriers (OR 0.22). 2

  • A systematic review of 12 studies concluded that women with family history of breast cancer do not significantly increase their disease risk by using OCPs, though some women who took OCPs prior to 1975 (higher-dose formulations) may have been at greater risk. 4

  • One historical cohort study found elevated risk among sisters and daughters of breast cancer probands who used OCPs (RR 3.3), particularly for use during or prior to 1975, but this was not seen with more recent formulations. 5

Critical Benefit: Ovarian Cancer Risk Reduction

OCPs provide substantial ovarian cancer risk reduction of 40-60%, which is particularly important for BRCA1/2 carriers who face high ovarian cancer risk. 6

  • This protective effect increases with longer duration of use and persists long after discontinuation. 6

  • For BRCA1/2 carriers specifically, ovarian cancer risk is reduced by 45-60%. 2

  • The ovarian cancer risk reduction benefit often outweighs the small breast cancer risk increase, especially in high-risk populations. 3, 2

Absolute Contraindications

OCPs are Category 4 (unacceptable health risk) in women with current breast cancer because breast cancer is hormonally sensitive and prognosis may worsen with hormonal exposure. 1

  • Past breast cancer with no evidence of disease for 5 years is Category 3 (risks usually outweigh benefits). 1

Clinical Decision-Making Algorithm

Step 1: Exclude Absolute Contraindications

  • Current or recent (<5 years) breast cancer diagnosis → Do not prescribe OCPs 1
  • Age ≥35 with smoking → Do not prescribe combined OCPs (cardiovascular risk exceeds breast cancer concerns) 1

Step 2: Assess Family History and Genetic Status

  • If strong family history exists, provide genetic counseling and testing before OCP initiation. 3, 2
  • For confirmed BRCA1/2 carriers, OCPs are acceptable for contraception given the substantial ovarian cancer risk reduction and lack of consistent evidence for increased breast cancer risk. 2
  • Consider low-dose formulations which may have more favorable risk profiles. 2

Step 3: Counsel on Risk-Benefit Balance

  • Emphasize that any breast cancer risk elevation is temporary and disappears within 10 years of stopping. 1
  • Highlight the 40-60% ovarian cancer risk reduction, which is permanent and increases with duration of use. 6
  • For young women, explain that relative risk increases translate to minimal absolute risk given low baseline breast cancer incidence. 1

Step 4: Ensure Appropriate Monitoring

  • Regular breast cancer screening is essential regardless of OCP use in women with family history or BRCA mutations. 3, 2
  • This should follow standard high-risk screening protocols, not be modified based on OCP use. 3

Common Pitfalls to Avoid

  • Do not overestimate absolute risk in young women: A relative risk of 1.5 in a 25-year-old represents minimal absolute risk increase given breast cancer rarity at that age. 1

  • Do not assume past OCP use permanently increases risk: Risk elevation resolves within 10 years of discontinuation. 1

  • Do not unnecessarily restrict OCPs in women with family history: Current evidence does not support significantly amplified risk in this population. 1, 4

  • Do not overlook the substantial ovarian cancer risk reduction benefit when focusing solely on breast cancer risk, especially in BRCA carriers. 3, 2

  • Do not apply data from pre-1975 high-dose formulations to modern low-dose OCPs: Historical studies showing elevated risk used formulations no longer available. 4, 5

References

Guideline

COCP and Breast Cancer Risk

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Estrogen-Based Birth Control with Family History of Breast Cancer

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Birth Control Pills in Patients with a Strong Family History of Breast Cancer

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.