October 03, 2014
4 min read
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Increased prostate, pancreatic cancer risks among BRCA mutation carriers support additional screening

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Individuals with BRCA2 mutations demonstrated significantly higher risks for pancreatic cancer and prostate cancer than noncarriers, according to study results.

Perspective from Susan M. Domchek, MD

The findings support current recommendations that BRCA mutation carriers undergo screening for malignancies other than breast and ovarian cancers, the researchers wrote.

Jacqueline Mersch, MS, CGC, who at the time of the study was a graduate student in the genetic counseling program at the University of Texas Graduate School of Biomedical Science at Houston, and colleagues sought to evaluate the incidence of malignancies other than breast and ovarian cancers in 1,072 patients who were identified as BRCA1 (n=613) or BRCA2 (n=459) mutation carriers. All patients (mean age, 49.3 years) received genetic counseling at The University of Texas MD Anderson Cancer Center.

“Our goals in defining the cancer spectrum associated with BRCA1 and BRCA2 mutations are to one, help better identify individuals and families at risk for hereditary breast and ovarian cancers, and two, prevent or detect cancers early in individuals with mutations through appropriate screening measures,” Mersch told HemOnc Today. “Additionally, MD Anderson had a large sample population of known mutation carriers who had not previously been analyzed in this way. It was important to look closely at the cancer history in these individuals.”

Overall, Mersch and colleagues identified 1,177 cancers — which included 30 different cancer types — in the study population. Researchers then compared the incidence of these cancers in the study population with their expected age-related incidence in the general population.

The incidence of pancreatic cancer was significantly greater among BRCA2 mutation carriers than in the general population (standardized incidence ratio [SIR]=21.74; 95% CI, 13.08-33.96). Researchers observed the association between BRCA2 mutations and pancreatic cancer in men (SIR=82.55; 95% CI, 39.52-151.84) and women (SIR=13.8; 95% CI, 6.3-26.21).

Men who harbored BRCA2 mutations also demonstrated a significantly increased risk for prostate cancer compared with the general population (SIR=4.89; 95% CI, 1.95-10.07).

Researchers observed a trend toward increased incidence of melanoma in individuals who harbored BRCA1 mutations (SIR=3.31; 95% CI, 1.51-6.28), and cervical cancer in women who harbored BRAC2 mutations (SIR=4.41; 95% CI, 1.61-9.599).

“Our findings uphold the current NCCN Clinical Practice Guidelines for screening and management of Hereditary Breast and Ovarian Cancer syndrome,” Mersch said. “Furthermore, the significantly higher rate of pancreatic cancer found in our sample population compared to previous studies emphasizes the need for effective pancreatic cancer screening for these high-risk individuals.”

These data also highlight the importance of genetic counselors, Mersch said.

“Future research into the families of these individuals will expand on the base of knowledge built in this study,” Mersch said. “The familial cancer history, obtained by a genetic counselor in a clinic visit, is a valuable tool for risk assessment and genetic testing. This research is currently underway with results expected early next year.”

Disclosure: One researcher reports funding from and steering committee roles with BioMarin, Bristol-Myers Squibb and Novartis.

Jacqueline Mersch, MS, CGC, can be reached at the UT Southwestern Simmons Comprehensive Cancer Center, 2201 Inwood Road, Dallas, TX 75390-9323; email: jacqueline.mersch@utsouthwestern.edu.