familial breast cancer

Last reviewed 11/2023

Up to 10% of breast cancer in western countries is due to genetic predisposition. Susceptibility to breast cancer appears to be inherited as an autosomal dominant with limited penetrance and may thus be inherited from either father or mother. About 5% of breast cancer is due to highly penetrant dominant genes.

More than five genes are thought to be involved. The most important appears to be the BRCA1 gene located on chromosome 17q. This has recently been cloned and thought to have mutations present at different regions. Other genes identified include BRCA2 on 13q and the p53 gene on 17p.

• BRCA1 carriers have a lifetime risk approaching 80% of developing breast cancer and an increased risk of ovarian cancer (40-60%) (1)
• BRCA2 confers a lower risk of ovarian cancer (20-30%) but is associated with an increased risk of a wider spectrum of other cancers including prostate cancer, pancreatic cancer, and an increased risk of male breast cancer
• in the UK general caucasian population - frequency of mutations in BRCA1 or BRCA2 is approximately 1/400; in the Ashkenazim population the frequency of these mutations is about 2% (1)
• management of breast cancers in BRCA1 and BRCA2 carriers is currently the same as for sporadic cases, except that bilateral mastectomy may be offered at the time of primary surgery because of the increased risk of development of breast cancer in the contralateral breast (about 4% per year) (1)

Characteristics of familial breast cancer include:

• early age of presentation
• several relatives are affected
• bilateral involvement is common
• history of related cancers - colorectal, ovary, endometrium

If a first-degree relative has breast carcinoma, the relative risk of developing breast carcinoma is 1.7 to 2.5. If a second-degree relative is affected, the relative risk is 1.5.

DNA tests are possible for a few suitable families.

Mutations in the CHEK2 gene may increase the risk of breast cancer two-fold (1).

Mutations in the TP53 gene increase the risk of a wide spectrum of tumours, including sarcomas, adrenocortical carcinomas, brain cancer, and very early onset breast cancer.

NICE suggest (4):

• Carrier probability at which genetic testing should be offered

  When available in secondary care, use a carrier probability calculation method with demonstrated acceptable performance (in calibration and discrimination), as well as family history, to determine who should be offered referral to a specialist genetic clinic. Examples of acceptable methods include BOADICEA and the Manchester scoring system
  

  • offer genetic testing in specialist genetic clinics to a relative with a personal history of breast and/or ovarian cancer if that relative has a combined BRCA1 and BRCA2 mutation carrier probability of 10% or more
  • offer genetic testing in specialist genetic clinics to a person with no personal history of breast or ovarian cancer if their combined BRCA1 and BRCA2 mutation carrier probability is 10% or more and an affected relative is unavailable for testing

  Breast cancer risk category

  	Near population risk	Moderate risk	High Risk *
  Lifetime risk from age 20	Less than 17%	Greater than 17% but less than 30%	30% or greater
  Risk between ages 40 and 50	Less than 3%	3-8%	Greater than 8%

  *This group includes known BRCA1, BRCA2 and TP53 mutations and rare conditions that carry an increased risk of breast cancer such as Peutz-Jegher syndrome (STK11), Cowden (PTEN) and familial diffuse gastric cancer (E-Cadherin)

• Surveillance for women with no personal history of breast cancer
  • Offer annual mammographic surveillance to women:
    • aged 40-49 years at moderate risk of breast cancer
    • aged 40-59 years at high risk of breast cancer but with a 30% or lower probability of being a BRCA or TP53 carrier
    • aged 40-59 years who have not had genetic testing but have a greater than 30% probability of being a BRCA carrier
    • aged 40-69 years with a known BRCA1 or BRCA2 mutation
      
      
  • Offer annual MRI surveillance to women:
    • aged 30-49 years who have not had genetic testing but have a greater than 30% probability of being a BRCA carrier
    • aged 30-49 years with a known BRCA1 or BRCA2 mutation
    • aged 20-49 years who have not had genetic testing but have a greater than 30% probability of being a TP53 carrier
    • aged 20-49 years with a known TP53 mutation
      
      
• Surveillance for women with a personal and family history of breast cancer
  • offer annual mammographic surveillance to all women aged 50-69 years with a personal history of breast cancer who:
    • remain at high risk of breast cancer (including those who have a BRCA1 or BRCA2 mutation), and
    • do not have a TP53 mutation
• offer annual MRI surveillance to all women aged 30-49 years with a personal history of breast cancer who remain at high risk of breast cancer, including those who have a BRCA1 or BRCA2 mutation
  
  
• Chemoprevention for women with no personal history of breast cancer
  • offer either tamoxifen or raloxifene for 5 years to postmenopausal women with a uterus and at high risk of breast cancer unless they have a past history or may be at increased risk of thromboembolic disease or endometrial cancer
    
    
• Risk-reducing mastectomy for women with no personal history of breast cancer
  • all women considering bilateral risk-reducing mastectomy should be able to discuss their breast reconstruction options (immediate and delayed) with a member of a surgical team with specialist oncoplastic or breast reconstructive skills

Reference:

1. Pulse (2005); 65(14):55-60.
2. Evans DGR et al. (1994). Familial breast cancer. BMJ; 308:183-7
3. McPherson et al. (1994). BMJ;309: 1004
4. NICE (June 2013). Familial breast cancer - Classification and care of people at risk of familial breast cancer and management of breast cancer and related risks in people with a family history of breast cancer