According to University of Washington
researchers, genetic testing
for breast cancer and ovarian cancer is not a perfect science. Between 2002 and 2005, 300 breast cancer patients,
who were at higher risk of cancer due to inherited genetic mutations of the BRCA 1 and BRCA 2 genes, were evaluated.
The researchers used multiple screening tests to identify mutations not only in the BRCA 1 and BRCA 2 genes, but also
other inherited mutations in other genes that may predict breast cancer, such as CHEK2, TP53 and PTEN. Of the women in the study, 17 percent of the patients carried mutations that went undetected, and 12 percent of them had BRCA1or BRCA2 genes that the standard tests missed. The failure of the standard tests was higher with women who were under 40 years of age at the time of breast cancer diagnosis.
In the U.S., 10 percent of women diagnosed with breast cancer have the BRCA genes. The researchers stated that the lifetime risk of breast cancer is as high as 80 percent for women who have mutations of BRCA1 and BRCA 2 genes. The risk of ovarian cancer is 40 percent or higher for women who have a BRCA 1 mutation, and 20 percent or higher for women who have the BRCA 2 mutation.











