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Knowledge of Genetic Risk for Breast Cancer Not Worth the Cost

Knowledge of Genetic Risk for Breast Cancer Not Worth the Cost

A new University of California, Los Angeles (UCLA) study findings that about seven percent of US women will be diagnosed with breast cancer by age 70, however, 50 percent of women with a BRCA1 or BRCA2 mutation will contract the cancer.

The mutation also increases the risk for ovarian cancer.

Despite the increased incidence, researchers question the value of screening for the genetic mutations in the general population — including those who do not have cancer or have no family history of the disease — because of the high cost.

Investigators found that compared with universal screening, other diagnostic tools remain more efficient and might be more cost-effective.

Dr. Patricia Ganz, director of the division of cancer prevention and control research at UCLA’s Jonsson Comprehensive Cancer Center, and Elisa Long, assistant professor at the UCLA Anderson School of Management concluded the BRCA genetic test that is most widely used today is too expensive to warrant universal screening, given how rare BRCA mutations are.

Currently, the commercial test sells for about $4,000.

“The cost of BRCA testing would need to drop by 90 percent for testing to be cost-effective for the whole population,” Ganz said.

Long and Ganz calculated that for every 10,000 women screened, BRCA screening could avert four cases of breast cancer and two cases of ovarian cancer more than family history-based testing would. But the BRCA screening would only extend patients’ life by an average of two days.

For 99.75 percent of women screened, a negative genetic test offers no increase in life expectancy, nor would it eliminate the need for regular mammograms, and it could provide false reassurance that a woman is not at risk for breast cancer.

The study builds upon previous work by other researchers that analyzed genetic screening of women of Ashkenazi Jewish descent, a population in which one out of every 50 women carries a harmful mutation.

The study is appears online in JAMA Oncology.

Because a larger percentage of this group were identified as BRCA mutation carriers, Long and Ganz found that the approach would yield an estimated 62 breast and 34 ovarian cancers averted per 10,000 women tested, and gains in life expectancy that were 16 times higher than with universal screening.

Notably, researchers explain that not all breast cancers are attributable to the BRCA genes. In fact, of the 233,000 breast cancers diagnosed annually in the United States, only five to 10 percent are attributable to mutations in the BRCA genes.

Women with breast cancer who carry these mutated genes usually develop the disease at a younger age, often in both breasts, and the cancer is often a more aggressive sub-type such as triple-negative breast cancer.

Harmful BRCA gene mutations are more likely to be found in families affected by breast and ovarian cancers, and carriers can pass the mutated genes to both daughters and sons.

Those who carry a BRCA mutation are thought to have a 45 to 80 percent lifetime risk of developing breast cancer. Women carrying the BRCA-1 mutation have up to a 39 percent lifetime risk; women with BRCA-2 have a 10 to 17 percent lifetime risk for ovarian cancer.

The U.S. Preventive Services Task Force advises BRCA genetic testing only for women with a known family history of breast, ovarian, tubal, or peritoneal cancer.

Long said that although the commercial test remains the most commonly used test for BRCA mutations, a new $249 test recently announced could encourage other companies to introduce lower-cost genetic tests — which could make universal screening more practical and more affordable.

She noted, however, that questions would remain about the feasibility of providing personalized genetic counseling services on such a large scale.

“It’s like looking for a needle in a haystack,” Long said.

“If only 1 in 400 women across the country have one or both of the BRCA-1 or BRCA-2 mutations, universal screening would cost $1 million to $2 million to detect a single BRCA mutation, or nearly $400 billion to screen all women in the U.S.

Perhaps this money could be better spent on other diagnostic tools for young women, such as MRIs, to have the greatest impact.”

Source: UCLA
DNA breast cancer photo by shutterstock.

Knowledge of Genetic Risk for Breast Cancer Not Worth the Cost

Rick Nauert PhD

Rick Nauert, PhDDr. Rick Nauert has over 25 years experience in clinical, administrative and academic healthcare. He is currently an associate professor for Rocky Mountain University of Health Professionals doctoral program in health promotion and wellness. Dr. Nauert began his career as a clinical physical therapist and served as a regional manager for a publicly traded multidisciplinary rehabilitation agency for 12 years. He has masters degrees in health-fitness management and healthcare administration and a doctoral degree from The University of Texas at Austin focused on health care informatics, health administration, health education and health policy. His research efforts included the area of telehealth with a specialty in disease management.

APA Reference
Nauert PhD, R. (2018). Knowledge of Genetic Risk for Breast Cancer Not Worth the Cost. Psych Central. Retrieved on December 3, 2020, from
Scientifically Reviewed
Last updated: 8 Aug 2018 (Originally: 7 Sep 2015)
Last reviewed: By a member of our scientific advisory board on 8 Aug 2018
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