Vaynrub Anna, Salazar Brian, Feng Yilin Eileen, West Harry, Michel Alissa, Umakanth Subiksha, Crew Katherine D, Kukafka Rita
Department of Medicine, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA.
Mailman School of Public Health, Columbia University Irving Medical Center, 630 West 168th St, New York, NY, 10032, USA.
BMC Cancer. 2025 Jan 7;25(1):19. doi: 10.1186/s12885-024-13408-x.
Despite the association of pathogenic variants (PVs) in cancer predisposition genes with significantly increased risk of breast cancer (BC), uptake of genetic testing (GT) remains low, especially among ethnic minorities. Our prior study identified that a patient decision aid, RealRisks, improved patient-reported outcomes (including worry and perceived risk) relative to standard educational materials. This study examined patients' GT experience and its influence on subsequent actions. We also sought to identify areas for improvement in RealRisks that would expand its focus from improved GT decision-making to understanding results.
Women enrolled in the parent randomized controlled trial were recruited and interviewed. Demographic data was collected from surveys in the parent study. Interviews were conducted, transcribed, and coded to identify recurring themes. Descriptive statistics were generated to compare the interviewed subgroup to the original study cohort of 187 women.
Of the 22 women interviewed, 11 (50%) had positive GT results, 2 (9.1%) with a BRCA1/2 PV, and 9 (40.9%) with variants of uncertain significance (VUS). Median age was 40.5 years and 15 (71.4%) identified as non-Hispanic. Twenty (90.9%) reported a family history of BC, and 2 (9.1%) reported a family history of BRCA1/2 PV. The emerging themes included a preference for structured communication of GT results and the need for more actionable knowledge to mitigate BC risk, especially among patients with VUS or negative results. Few patients reported lifestyle changes following the return of their results, although they did understand that their behaviors can impact their BC risk.
Patients preferred a structured explanation of their GT results to facilitate a more personal testing experience. While most did not change lifestyle behaviors in response to their GT results, there was a consistent call for further guidance following the initial discussion of GT results. Empowering patients, especially those with negative or VUS results, with the context to internalize the implications of their results and form accurate risk perception represents a powerful opportunity to optimize subsequent risk management strategies. Informed by this study, future work will expand RealRisks to include the return of results and decision support to navigate concrete next steps.
尽管癌症易感基因中的致病变异(PVs)与乳腺癌(BC)风险显著增加相关,但基因检测(GT)的接受度仍然很低,尤其是在少数族裔中。我们之前的研究发现,与标准教育材料相比,患者决策辅助工具RealRisks改善了患者报告的结果(包括担忧和感知风险)。本研究调查了患者的基因检测体验及其对后续行动的影响。我们还试图确定RealRisks中需要改进的领域,将其重点从改善基因检测决策扩大到理解检测结果。
招募参与母本随机对照试验的女性并进行访谈。从母本研究的调查中收集人口统计学数据。进行访谈、转录并编码以识别反复出现的主题。生成描述性统计数据,将接受访谈的亚组与187名女性的原始研究队列进行比较。
在接受访谈的22名女性中,11名(50%)基因检测结果为阳性,2名(9.1%)携带BRCA1/2 PV,9名(40.9%)携带意义未明的变异(VUS)。中位年龄为40.5岁,15名(71.4%)被认定为非西班牙裔。20名(90.9%)报告有乳腺癌家族史,2名(9.1%)报告有BRCA1/2 PV家族史。新出现的主题包括倾向于以结构化方式传达基因检测结果,以及需要更多可采取行动的知识来降低乳腺癌风险,尤其是在携带VUS或检测结果为阴性的患者中。很少有患者报告在收到检测结果后改变生活方式,尽管他们明白自己的行为会影响患乳腺癌的风险。
患者更喜欢对其基因检测结果进行结构化解释,以促进更个性化的检测体验。虽然大多数人没有因基因检测结果而改变生活方式,但在首次讨论基因检测结果后,一直有人呼吁提供进一步指导。让患者,尤其是那些检测结果为阴性或携带VUS的患者,了解其结果的含义并形成准确的风险认知,这是优化后续风险管理策略的一个有力机会。基于本研究,未来的工作将扩展RealRisks,使其包括检测结果反馈和决策支持,以指导具体的下一步行动。