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Your Breast Cancer Risk Checklist: 3 Steps

Based on U.S. Preventive Services Task Force, BRCA-Related Cancer: Risk Assessment, Genetic Counseling and Genetic Testing

How family history changes breast cancer screening, who should consider genetic counseling, who counts as high risk, and what dense breasts mean.

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In this guide

Questions for Relatives

  • Who had cancer, and which kind?
  • How old were they at diagnosis?
  • Did anyone test for BRCA changes?

Easy to Overlook

  • Your father's side counts too
  • Ovarian, tubal and peritoneal cancer
  • Past radiation to your chest

Questions for Your Provider

  • Do I need a risk assessment?
  • What does dense tissue mean for me?
  • Should I see a genetic counselor?

What the guideline says

  • About 1 in 8 U.S. women will be diagnosed with breast cancer in her lifetime, according to the American Cancer Society.
  • For women at average risk, the current guideline is a mammogram every two years from age 40 through 74.
  • The U.S. Preventive Services Task Force recommends a brief risk assessment for women with a personal or family history of breast, ovarian, tubal or peritoneal cancer, or with ancestry linked to BRCA1 or BRCA2 gene changes.
  • If that assessment points to higher risk, the next step is genetic counseling and, if appropriate, genetic testing; women without those histories do not need routine genetic testing.
  • For women at high risk, the American Cancer Society recommends a breast MRI and a mammogram every year, typically starting at age 30.
  • Dense breast tissue makes cancer harder to see and slightly raises risk, so ask your provider whether more imaging makes sense for you.

Source: U.S. Preventive Services Task Force, BRCA-Related Cancer: Risk Assessment, Genetic Counseling and Genetic Testing

Read the full article: Breast Cancer: Family History, Genetic Testing and When to Start Screening Early →

This guide is general health information and does not replace advice from your own provider.

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