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基于关键风险因素(家族史、乳腺密度和多基因风险)的乳腺癌风险预测模型的验证。

Validation of a breast cancer risk prediction model based on the key risk factors: family history, mammographic density and polygenic risk.

机构信息

Genetic Technologies Limited, 60-66 Hanover St, Fitzroy, VIC, 3065, Australia.

Channing Division of Network Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

出版信息

Breast Cancer Res Treat. 2023 Apr;198(2):335-347. doi: 10.1007/s10549-022-06834-7. Epub 2023 Feb 7.

Abstract

PURPOSE

We compared a simple breast cancer risk prediction model, BRISK (which includes mammographic density, polygenic risk and clinical factors), against a similar model with more risk factors (simplified Rosner) and against two commonly used clinical models (Gail and IBIS).

METHODS

Using nested case-control data from the Nurses' Health Study, we compared the models' association, discrimination and calibration. Classification performance was compared between Gail and BRISK for 5-year risks and between IBIS and BRISK for remaining lifetime risk.

RESULTS

The odds ratio per standard deviation was 1.43 (95% CI 1.32, 1.55) for BRISK 5-year risk, 1.07 (95% CI 0.99, 1.14) for Gail 5-year risk, 1.72 (95% CI 1.59, 1.87) for simplified Rosner 10-year risk, 1.51 (95% CI 1.41, 1.62) for BRISK remaining lifetime risk and 1.26 (95% CI 1.16, 1.36) for IBIS remaining lifetime risk. The area under the receiver operating characteristic curve (AUC) was improved for BRISK over Gail for 5-year risk (AUC = 0.636 versus 0.511, P < 0.0001) and for BRISK over IBIS for remaining lifetime risk (AUC = 0.647 versus 0.571, P < 0.0001). BRISK was well calibrated for the estimation of both 5-year risk (expected/observed [E/O] = 1.03; 95% CI 0.73, 1.46) and remaining lifetime risk (E/O = 1.01; 95% CI 0.86, 1.17). The Gail 5-year risk (E/O = 0.85; 95% CI 0.58, 1.24) and IBIS remaining lifetime risk (E/O = 0.73; 95% CI 0.60, 0.87) were not well calibrated, with both under-estimating risk. BRISK improves classification of risk compared to Gail 5-year risk (NRI = 0.31; standard error [SE] = 0.031) and IBIS remaining lifetime risk (NRI = 0.287; SE = 0.035).

CONCLUSION

BRISK performs better than two commonly used clinical risk models and no worse compared to a similar model with more risk factors.

摘要

目的

我们比较了一个简单的乳腺癌风险预测模型 BRISK(包括乳腺密度、多基因风险和临床因素),与一个具有更多风险因素的类似模型(简化的 Rosner),以及两个常用的临床模型(Gail 和 IBIS)。

方法

使用来自护士健康研究的嵌套病例对照数据,我们比较了模型的关联性、区分度和校准度。使用 Gail 和 BRISK 比较了 5 年风险的分类性能,使用 IBIS 和 BRISK 比较了剩余终生风险的分类性能。

结果

BRISK 5 年风险的比值比为 1.43(95%置信区间 1.32,1.55),Gail 5 年风险的比值比为 1.07(95%置信区间 0.99,1.14),简化 Rosner 10 年风险的比值比为 1.72(95%置信区间 1.59,1.87),BRISK 剩余终生风险的比值比为 1.51(95%置信区间 1.41,1.62),IBIS 剩余终生风险的比值比为 1.26(95%置信区间 1.16,1.36)。BRISK 对 Gail 5 年风险的曲线下面积(AUC)改善(AUC=0.636 比 0.511,P<0.0001),对 IBIS 剩余终生风险的 AUC 改善(AUC=0.647 比 0.571,P<0.0001)。BRISK 对 5 年风险(预期/观察[E/O]=1.03;95%置信区间 0.73,1.46)和剩余终生风险(E/O=1.01;95%置信区间 0.86,1.17)的估计都很好地校准。Gail 5 年风险(E/O=0.85;95%置信区间 0.58,1.24)和 IBIS 剩余终生风险(E/O=0.73;95%置信区间 0.60,0.87)则没有很好地校准,都低估了风险。BRISK 与 Gail 5 年风险(NRI=0.31;标准误差[SE]=0.031)和 IBIS 剩余终生风险(NRI=0.287;SE=0.035)相比,提高了风险分类的准确性。

结论

BRISK 优于两个常用的临床风险模型,且与具有更多风险因素的类似模型相比表现不差。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff09/10020257/0cd706359946/10549_2022_6834_Fig1_HTML.jpg

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