Department of Internal Medicine, King Hussein Cancer Center, 202 Queen Rania Al Abdullah Street, P.O. Box: 1269, Amman, 11941, Jordan.
School of Medicine, The University of Jordan, Amman, Jordan.
Sci Rep. 2024 Jun 4;14(1):12820. doi: 10.1038/s41598-024-63300-8.
Genetic counseling and testing are more accessible than ever due to reduced costs, expanding indications and public awareness. Nonetheless, many patients missed the opportunity of genetic counseling and testing due to barriers that existed at that time of their cancer diagnoses. Given the identified implications of pathogenic mutations on patients' treatment and familial outcomes, an opportunity exists to utilize a 'traceback' approach to retrospectively examine their genetic makeup and provide consequent insights to their disease and treatment. In this study, we identified living patients diagnosed with breast cancer (BC) between July 2007 and January 2022 who would have been eligible for testing, but not tested. Overall, 422 patients met the eligibility criteria, 282 were reached and invited to participate, and germline testing was performed for 238, accounting for 84.4% of those invited. The median age (range) was 39.5 (24-64) years at BC diagnosis and 49 (31-75) years at the date of testing. Genetic testing revealed that 25 (10.5%) patients had pathogenic/likely pathogenic (P/LP) variants; mostly in BRCA2 and BRCA1. We concluded that long overdue genetic referral through a traceback approach is feasible and effective to diagnose P/LP variants in patients with history of BC who had missed the opportunity of genetic testing, with potential clinical implications for patients and their relatives.
由于成本降低、适应证扩大和公众意识提高,遗传咨询和检测比以往任何时候都更容易获得。尽管如此,由于癌症诊断时存在的障碍,许多患者仍然错过了遗传咨询和检测的机会。鉴于致病性突变对患者治疗和家族结局的影响,有机会利用“回溯”方法来回顾性检查他们的基因构成,并为他们的疾病和治疗提供相应的见解。在这项研究中,我们确定了在 2007 年 7 月至 2022 年 1 月期间被诊断患有乳腺癌(BC)的存活患者,这些患者有资格进行检测,但未进行检测。共有 422 名患者符合入选标准,其中 282 名患者被联系并邀请参加,对 238 名患者进行了种系检测,占受邀患者的 84.4%。BC 诊断时的中位年龄(范围)为 39.5(24-64)岁,检测时的中位年龄(范围)为 49(31-75)岁。遗传检测显示,25 名(10.5%)患者存在致病性/可能致病性(P/LP)变异,主要在 BRCA2 和 BRCA1 中。我们得出结论,通过回溯方法进行遗传转诊是可行且有效的,可以在错过遗传检测机会的 BC 病史患者中诊断出 P/LP 变异,这对患者及其亲属具有潜在的临床意义。