Clare Scott, Walter and Eliza Hall Institute
Following her 2013 announcement in the op-ed pages of The New York Times that she was having a double mastectomy, US actress Angelina Jolie Pitt has published another piece this week discussing her decision to have her ovaries and fallopian tubes removed to mitigate her high genetic risk of cancer.
Jolie Pitt carries a faulty BRCA1 gene, which predisposes women to developing breast and ovarian cancer. Three women in her family – her mother, aunt and grandmother – were diagnosed with breast or ovarian cancer while still under the age of 60. All three died of their illness.
The publicity surrounding her double mastectomy led to what researchers and the media have dubbed the “Jolie effect”. An Australian study published six months after Jolie Pitt’s disclosure found referrals to familial cancer centres in Victoria more than doubled, and 64% involved people with a high risk of breast cancer. A similar UK study showed that in the year following her May 2013 announcement, referrals to 12 family history clinics increased over twofold.
But ovarian cancer, as you will see, is very different to breast cancer in that it’s very rare. So those of us who work in the field actually hope there’s no Jolie effect in this instance because it’s likely to cause a lot of worry to women who don’t need to be concerned and to divert resources away from those who do.
BRCA and cancer risk
The genes known as BRCA1 and BRCA2 usually help prevent cancers. Everyone has two copies of both but, in some people, one of the copies of either has an error or fault so it doesn’t work properly. The result is a high risk of developing breast and ovarian cancer at younger ages than usual.
The lifetime risk of ovarian cancer for a woman with a faulty BRCA1 gene is about 40% to 60%. This risk increases from her late 30s and continues on an upward trajectory with age. Breast cancer risk is also higher for these women and can be up to 80% depending on family history.