Mayo Clinic: Recent large-scale genomic analyses have uncovered dozens of common genetic variants that are associated with breast cancer. Each variant, however, contributes only a tiny amount to a person’s overall risk of developing the disease. A Mayo Clinic-led team of
international researchers has now combined 77 of these common genetic
variants into a single risk factor that can be used to improve the
identification of women with an elevated risk of breast cancer. This
factor, known as a polygenic risk score, was built from the genetic data
of more than 67,000 women. The results of the research are published
April 9, 2015, in the Journal of the National Cancer Institute (JNCI).
A companion study has extended this finding to show that this measure
of genetic variation can be combined with traditional predictors of
breast cancer risk such as breast density and family history to improve personalized estimates of breast cancer risk. Those findings appeared in JNCI last month.
“This genetic risk factor adds valuable information to what we
already know can affect a woman’s chances of developing breast cancer,”
says study co-author Celine Vachon, Ph.D.,
an epidemiologist at Mayo Clinic. “We are currently developing a test
based on these results, and though it isn’t ready for clinical use yet, I
think that within the next few years we will be using this approach for
better personalized screening and prevention strategies for our
patients.”
Scientists have known for decades that genetics can play a role in breast cancer. For example, inheriting a mutation in BRCA1 and BRCA2
genes greatly increase a woman’s risk of developing the disease, but
these mutations are rare and account for less than five percent of all
breast cancers. More common genetic variations known as single
nucleotide polymorphisms or SNPs also contribute to cancer
susceptibility, but the individual contributions are too small to
predict breast cancer risk.
In this study, researchers tested whether they could combine the
effects of these individual SNPs into a single risk factor for breast
cancer. The investigators essentially added up information on 77 SNPs
from 33,673 breast cancer patients and 33,381 healthy subjects to derive
the polygenic risk score.
They showed that the polygenic risk score could successfully place
women into different categories of risk. Compared to women with an
average polygenic risk score, women in the top 1 percent were three
times more likely to develop breast cancer. In addition, women in the
lowest one percent of the score were at a 70 percent lower risk of
developing breast cancer. These results indicate that the polygenic risk
score is as powerful as other known risk factors such as breast density
or family history.
“To do an even better job at risk prediction, we need to include this
genetic profile into breast cancer risk models, along with other
relevant information like family history, lifestyle risk factors,
previous biopsies, and breast density,” says study co-author Fergus Couch, Ph.D.,
a molecular geneticist and pathologist at Mayo Clinic. “But first we
need to make sure that each of the factors are independent, because if
the polygenic risk score is simply repeating what was already accounted
for by some of the other known risk factors then it won’t be valuable in
a risk model setting.”
Drs. Couch and Vachon conducted a second study to evaluate overlap between the polygenic risk score and the Breast Imaging Reporting and Data System
(BI-RADS), a breast density measure that is routinely assessed in the
clinical setting. Using data from three clinical studies involving 1,643
breast cancer patients and 2,397 healthy subjects, the researchers
found that both factors independently contribute information to breast
cancer risk.
They incorporated the polygenic risk score into the Breast Cancer Surveillance Consortium (BCSC) risk-prediction model,
which uses breast density, family history of breast cancer, history of
breast biopsy, age and ethnicity to calculate breast cancer risk. The
researchers then compared the five-year risk prediction calculated using
the BCSC model with and without the genetic information. The addition
of the polygenic risk score improved the performance of the model,
helping to place 11 percent of women who eventually got cancer into a
higher risk category where they would have been likely to benefit from
interventions such as MRIs, chemoprevention, or even prophylactic mastectomies.
The findings suggest that both breast density and common genetic
variation are important for risk prediction and should be included in
clinical models. However, the researchers say that larger studies are
still needed to test the ability of these models to estimate risk in the
general population.
“There have been a lot of common genetic variants associated with cancers, not just for breast cancer but also for ovarian cancer and prostate cancer,
but so far we haven’t seen these being used in clinical practice,” says
Dr. Vachon. “In the future, these factors are going to be helpful in
defining who is at highest and lowest risk of cancer and help both
patients and clinicians make better decisions about their care.”