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NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic, Version 1.2020

Mary Beryl Daly, Robert Pilarski, Matthew B.B. Yurgelun, Michael P. Berry, Saundra S. Buys, Patricia Dickson, Susan M. Domchek, Ahmed M. Elkhanany, Susan Friedman, Judy Ellen Garber, Michael Goggins, Mollie L. Hutton, Seema Khan, Catherine E. Klein, Wendy K. Kohlmann, Allison W. Kurian, Christine Laronga, Jennifer Keating Litton, Julie S. Mak, Carolyn S. Menendez, Sofia Diana Merajver, Barbara M. Norquist, Kenneth Offit, Tuya Pal, Holly Jane Pederson, Gwen Reiser, Kristen Mahoney Shannon, Kala Visvanathan, Jeffrey N. Weitzel, Myra J. Wick

📄 Abstract

The NCCN Guidelines for Genetic/Familial High-Risk Assessment: Breast, Ovarian, and Pancreatic provide recommendations for genetic testing and counseling for hereditary cancer syndromes, and risk management recommendations for patients who are diagnosed with syndromes associated with an increased risk of these cancers. The NCCN panel meets at least annually to review comments, examine relevant new data, and reevaluate and update recommendations. These NCCN Guidelines Insights summarize the panel’s discussion and most recent recommendations regarding criteria for high-penetrance genes associated with breast and ovarian cancer beyond BRCA1/2, pancreas screening and genes associated with pancreatic cancer, genetic testing for the purpose of systemic therapy decision-making, and testing for people with Ashkenazi Jewish ancestry.

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