Who needs genetic testing for breast cancer?
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CLEVELAND – (October 3, 2018) – Advances are regularly being made in cancer genetics. But, if patients aren’t screened and diagnosed early enough, the advances can’t save lives. A presentation at The North American Menopause Society (NAMS) Annual Meeting in San Diego, October 3-6, will review the various genetic testing options for breast cancer, as well as profile those who should be tested.

It is estimated that 12-14% of breast cancers are related to hereditary cancer predisposition syndromes. That means nearly 35,000 cases of breast cancer every year are attributable to hereditary risk. When breast cancer is detected early enough, women have significantly better chances of survival. Those chances increase if the probability of getting breast cancer can be decreased through the use of various preventive medications and risk-reducing surgical procedures.

In her presentation at the upcoming NAMS Annual Meeting, Dr. Holly Pederson from the Cleveland Clinic will provide compelling data designed to encourage healthcare providers to be more proactive in identifying those patients most at risk and when to recommend genetic counseling and testing. She will discuss the various advances in genetic testing, including multigene panel testing, which is proving to be more effective and cost-efficient, as well

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