Experiences of Family Communication and Cascade Genetic Testing for Hereditary Cancer in Medically Underserved Populations-A Qualitative Study.

Erica M Bednar, J Alejandro Rauh-Hain, Jose J Garcia, Norma de Aguinaga, Mary Anne Powell, Sylvia L Peral, Roni Nitecki, Kirsten Jorgensen, Natasha L Rudy, Karen H Lu, Charles A Leath, Isabel C Scarinci
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Abstract

We sought to explore the intrafamilial communication and cascade genetic testing (CGT) experiences of patients with hereditary cancer from diverse, medically underserved populations and their relatives. Participants included patients receiving oncology care at an urban, safety net hospital in Texas or comprehensive cancer center in Alabama and their first-degree relatives. In-depth semi-structured qualitative interviews were completed wherein patients shared their experiences with genetic counseling (GC), genetic testing (GT), and communicating their results to relatives. Relatives shared their experiences receiving information from the patient and considering CGT. Interviews were transcribed, coded, and themes were identified. Of 25 participating patients, most recalled key aspects of GC and their GT results. Most (80%) patients shared their results with relatives, but only some relatives underwent CGT; patients reported low perceived susceptibility to hereditary cancer as a common barrier to CGT for their relatives. Of 16 participating relatives, most reported feeling distress upon learning the patient's GT results. Relatives were fearful of learning their own CGT results but identified prevention and early detection as CGT benefits. Interviews identified opportunities during family communication to improve relatives' perceived susceptibility to hereditary cancer. Tailored resources may support patients and relatives experiencing distress and fear during GT.

Prevention relevance: This study of intrafamilial communication and cascade genetic testing experiences of patients with hereditary cancer and their relatives from diverse, medically underserved populations identified relatives' perceived susceptibility to hereditary cancer risks, distress, and fear as frequent reactions and barriers to testing. These results may inform future hereditary cancer prevention efforts.

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医学服务不足人群中遗传性癌症的家庭沟通和连锁基因检测经验——定性研究。
我们试图探索来自不同医疗服务不足人群的遗传性癌症患者及其亲属的家族内沟通和级联基因检测(CGT)经验。参与者包括在得克萨斯州城市安全网医院或阿拉巴马州癌症综合中心接受肿瘤治疗的患者及其一级亲属。完成了深入的半结构化定性访谈,患者分享了他们的基因咨询(GC)、基因检测(GT)经验,并将结果传达给亲属。亲属们分享了他们从患者那里获得信息并考虑CGT的经历。访谈被转录、编码,并确定了主题。在25名参与的患者中,大多数人回忆起GC的关键方面及其GT结果。大多数(80%)患者与亲属分享他们的结果,但只有一些亲属接受了CGT;患者报告称,遗传性癌症易感性较低,这是其亲属CGT的常见障碍。在16名参与的亲属中,大多数人在得知患者的GT结果后感到痛苦。亲属们害怕了解自己的CGT结果,但认为预防和早期检测是CGT的好处。访谈确定了在家庭沟通过程中改善亲属对遗传性癌症易感性的机会。量身定制的资源可以支持在GT期间经历痛苦和恐惧的患者和亲属。
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