Chana Wiesman1,2, Esther Rose1,2, Allison Grant2, Adam Zimilover2, Susan Klugman1,2, Nicole Schreiber-Agus1,2,3. 1. Department of Obstetrics &Gynecology and Women's Health, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, New York, USA. 2. Program for Jewish Genetic Health, Albert Einstein College of Medicine/Montefiore Medical Center, Bronx, New York, USA. 3. Department of Genetics, Albert Einstein College of Medicine, Bronx, New York, USA.
Abstract
PURPOSE: The notion of offering population-based screening to the Ashkenazi Jewish (AJ) population for the BRCA1/2 founder mutations continues to gain support. A program called the BRCAcommunity initiative was designed to identify the benefits and barriers associated with implementing this screening in a clinical setting. METHODS: Interested AJ individuals were stratified into high-risk (HR) and low-risk (LR) groups based on self-reported cancer histories. Those at HR were offered traditional genetic counseling/testing; those at LR were offered group genetic counseling and subsidized AJ BRCA founder mutation testing. RESULTS: During the pilot year, 62% of initial registrants and 53% of ultimate study participants were classified into the HR group. Among the 101 HR and 88 LR study participants, 8 and 2 BRCA carriers were identified, respectively. The LR carriers would have been missed by current mechanisms. Survey responses provided insight into the motivations and fears associated with pursuing testing, the efficacy of the initiative design, and challenges that exist on multiple levels, including the community, health-care providers, and insurance coverage. CONCLUSION: Although the medical value of identifying presymptomatic BRCA carriers in Ashkenazi Jews is evident, further measures need to be taken before this effort can be accomplished on a large scale.Genet Med advance online publication 13 October 2016.
PURPOSE: The notion of offering population-based screening to the Ashkenazi Jewish (AJ) population for the BRCA1/2 founder mutations continues to gain support. A program called the BRCAcommunity initiative was designed to identify the benefits and barriers associated with implementing this screening in a clinical setting. METHODS: Interested AJ individuals were stratified into high-risk (HR) and low-risk (LR) groups based on self-reported cancer histories. Those at HR were offered traditional genetic counseling/testing; those at LR were offered group genetic counseling and subsidized AJ BRCA founder mutation testing. RESULTS: During the pilot year, 62% of initial registrants and 53% of ultimate study participants were classified into the HR group. Among the 101 HR and 88 LR study participants, 8 and 2 BRCA carriers were identified, respectively. The LR carriers would have been missed by current mechanisms. Survey responses provided insight into the motivations and fears associated with pursuing testing, the efficacy of the initiative design, and challenges that exist on multiple levels, including the community, health-care providers, and insurance coverage. CONCLUSION: Although the medical value of identifying presymptomatic BRCA carriers in Ashkenazi Jews is evident, further measures need to be taken before this effort can be accomplished on a large scale.Genet Med advance online publication 13 October 2016.
Authors: Meghna S Trivedi; Hilary Colbeth; Haeseung Yi; Alejandro Vanegas; Rebecca Starck; Wendy K Chung; Paul S Appelbaum; Rita Kukafka; Isaac Schechter; Katherine D Crew Journal: Public Health Genomics Date: 2019-06-04 Impact factor: 2.000
Authors: Kelly M Morgan; Jada G Hamilton; Heather Symecko; Daniella Kamara; Colby Jenkins; Jenny Lester; Kelsey Spielman; Lydia E Pace; Camila Gabriel; Jeffrey D Levin; Prince Rainier Tejada; Anthony Braswell; Vanessa Marcell; Temima Wildman; Bryan Devolder; Robin Camhi Baum; Jeremy N Block; Yuri Fesko; Kylin Boehler; Victoria Howell; Jacob Heitler; Mark E Robson; Katherine L Nathanson; Nadine Tung; Beth Y Karlan; Susan M Domchek; Judy E Garber; Kenneth Offit Journal: Genet Med Date: 2021-12-03 Impact factor: 8.864
Authors: Jeanna M McCuaig; Susan Randall Armel; Melanie Care; Alexandra Volenik; Raymond H Kim; Kelly A Metcalfe Journal: Cancers (Basel) Date: 2018-11-13 Impact factor: 6.639
Authors: Muin J Khoury; M Scott Bowen; Mindy Clyne; W David Dotson; Marta L Gwinn; Ridgely Fisk Green; Katherine Kolor; Juan L Rodriguez; Anja Wulf; Wei Yu Journal: Genet Med Date: 2017-12-14 Impact factor: 8.822