Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah, USA.
Department of Communication, University of Utah, Salt Lake City, Utah, USA.
J Genet Couns. 2022 Apr;31(2):470-478. doi: 10.1002/jgc4.1513. Epub 2021 Sep 27.
Women with a personal history of breast or ovarian cancer who previously had BRCA1/2 testing now have the opportunity for additional genetic risk information through multi-gene panel testing. However, little is known about women's receptivity to further contact and uptake of genetic counseling and updated genetic testing. Utilizing a clinic database to identify potential participants, we prospectively contacted women in the United States with a personal and/or family history of breast or ovarian cancer who had negative BRCA1/2 testing, which was performed primarily between 2011 and 2018. Eligible and interested participants were scheduled for a genetic counseling appointment to discuss updated genetic testing using a multi-gene panel. We attempted to contact 455 participants, screened 203 (45%), and 103 (23%) completed a pre-test genetic counseling visit to discuss updated testing. Of these, 88 participants had updated multi-gene panel testing. Participants had an average age of 59 years, and most (78%) had breast cancer with an average age of 45 at diagnosis. The majority (97%) of participants were white. Of participants who underwent panel testing, 13% (n = 11) had at least one pathogenic variant identified. Most participants (86%) had an out-of-pocket cost of $100 or less for their panel. There is a sizable population of women with a personal and/or family history of breast or ovarian cancer and negative BRCA1/2 test results who would qualify for updated multi-gene panel testing. In our study, 59% of those reached who were eligible completed a pre-test genetic counseling visit. Clinics could consider an outreach program to offer genetic counseling and updated genetic testing. Supports for this type of effort may include coordinators and genetic counseling assistants and an available database with patients' contact information and prior genetic test results. Updated testing allows women more information about their risk and may expand the value of genetic counseling.
曾接受过 BRCA1/2 检测的有乳腺癌或卵巢癌个人或家族病史的女性,现在有机会通过多基因面板检测获得更多的遗传风险信息。然而,人们对女性对进一步接触和接受遗传咨询和更新的基因检测的接受程度知之甚少。我们利用一个诊所数据库来确定潜在的参与者,前瞻性地联系了在美国有乳腺癌或卵巢癌个人或家族病史且 BRCA1/2 检测结果为阴性的女性,这些检测主要是在 2011 年至 2018 年之间进行的。符合条件且有兴趣的参与者被安排进行遗传咨询预约,讨论使用多基因面板进行更新的基因检测。我们试图联系 455 名参与者,筛选出 203 名(45%),其中 103 名(23%)完成了预测试遗传咨询访问,以讨论更新的检测。其中 88 名参与者进行了更新的多基因面板检测。参与者的平均年龄为 59 岁,大多数(78%)患有乳腺癌,诊断时的平均年龄为 45 岁。大多数参与者(97%)是白人。在接受面板检测的参与者中,有 13%(n=11)至少有一个致病性变异被检出。大多数参与者(86%)的面板检测费用在 100 美元或以下。有相当一部分有乳腺癌或卵巢癌个人或家族病史且 BRCA1/2 检测结果为阴性的女性符合更新的多基因面板检测条件。在我们的研究中,符合条件的参与者中有 59%完成了预测试遗传咨询访问。诊所可以考虑开展外展项目,提供遗传咨询和更新的基因检测。此类工作的支持可能包括协调员和遗传咨询助理,以及一个可用的数据库,其中包含患者的联系信息和之前的基因检测结果。更新的检测可以为女性提供更多有关其风险的信息,并可能扩大遗传咨询的价值。