Division of Cancer Epidemiology and Genetics, National Cancer Institute of Health, 9609 Medical Center Drive 7E-342, Rockville, MD, 20850, USA.
Division of Genetics and Epidemiology, The Institute of Cancer Research, London, UK.
Breast Cancer Res. 2021 Feb 15;23(1):22. doi: 10.1186/s13058-021-01399-7.
The Breast and Ovarian Analysis of Disease Incidence and Carrier Estimation Algorithm (BOADICEA) and the Tyrer-Cuzick breast cancer risk prediction models are commonly used in clinical practice and have recently been extended to include polygenic risk scores (PRS). In addition, BOADICEA has also been extended to include reproductive and lifestyle factors, which were already part of Tyrer-Cuzick model. We conducted a comparative prospective validation of these models after incorporating the recently developed 313-variant PRS.
Calibration and discrimination of 5-year absolute risk was assessed in a nested case-control sample of 1337 women of European ancestry (619 incident breast cancer cases) aged 23-75 years from the Generations Study.
The extended BOADICEA model with reproductive/lifestyle factors and PRS was well calibrated across risk deciles; expected-to-observed ratio (E/O) at the highest risk decile :0.97 (95 % CI 0.51 - 1.86) for women younger than 50 years and 1.09 (0.66 - 1.80) for women 50 years or older. Adding reproductive/lifestyle factors and PRS to the BOADICEA model improved discrimination modestly in younger women (area under the curve (AUC) 69.7 % vs. 69.1%) and substantially in older women (AUC 64.6 % vs. 56.8%). The Tyrer-Cuzick model with PRS showed evidence of overestimation at the highest risk decile: E/O = 1.54(0.81 - 2.92) for younger and 1.73 (1.03 - 2.90) for older women.
The extended BOADICEA model identified women in a European-ancestry population at elevated breast cancer risk more accurately than the Tyrer-Cuzick model with PRS. With the increasing availability of PRS, these analyses can inform choice of risk models incorporating PRS for risk stratified breast cancer prevention among women of European ancestry.
乳腺癌和卵巢疾病发生率及携带者估计算法(BOADICEA)和 Tyrer-Cuzick 乳腺癌风险预测模型在临床实践中被广泛应用,最近已扩展到包括多基因风险评分(PRS)。此外,BOADICEA 还扩展到包括生殖和生活方式因素,这些因素已经是 Tyrer-Cuzick 模型的一部分。我们在纳入最近开发的 313 变体 PRS 后,对这些模型进行了比较前瞻性验证。
在世代研究中,对 1337 名欧洲裔(619 名乳腺癌病例)年龄在 23-75 岁的嵌套病例对照样本中,评估了 5 年绝对风险的校准和区分。
具有生殖/生活方式因素和 PRS 的扩展 BOADICEA 模型在风险十分位数中具有良好的校准;在最高风险十分位数的预期与观察比(E/O):对于年龄小于 50 岁的女性为 0.97(95%CI 0.51-1.86),对于 50 岁或以上的女性为 1.09(0.66-1.80)。将生殖/生活方式因素和 PRS 添加到 BOADICEA 模型中,可适度提高年轻女性的区分度(曲线下面积(AUC)69.7%vs.69.1%),并可大幅提高老年女性的区分度(AUC 64.6%vs.56.8%)。具有 PRS 的 Tyrer-Cuzick 模型在最高风险十分位数中存在高估的证据:对于年轻女性,E/O=1.54(0.81-2.92),对于老年女性,E/O=1.73(1.03-2.90)。
在欧洲裔人群中,扩展的 BOADICEA 模型比具有 PRS 的 Tyrer-Cuzick 模型更准确地识别出处于较高乳腺癌风险的女性。随着 PRS 的日益普及,这些分析可以为欧洲裔女性基于 PRS 的乳腺癌风险分层预防选择风险模型提供信息。