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Per Med. 2005 Mar;2(1):49-79. doi: 10.1517/17410541.2.1.49.
2
Comparing the value of mammographic features and genetic variants in breast cancer risk prediction.比较乳腺钼靶特征和基因变异在乳腺癌风险预测中的价值。
AMIA Annu Symp Proc. 2014 Nov 14;2014:1228-37. eCollection 2014.
3
New genetic variants improve personalized breast cancer diagnosis.新的基因变异有助于改善个性化乳腺癌诊断。
AMIA Jt Summits Transl Sci Proc. 2014 Apr 7;2014:83-9. eCollection 2014.
4
Radiogenomics: the search for genetic predictors of radiotherapy response.放射基因组学:寻找放疗反应的基因预测指标。
Future Oncol. 2014 Dec;10(15):2391-406. doi: 10.2217/fon.14.173.
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Pursuing optimal thresholds to recommend breast biopsy by quantifying the value of tomosynthesis.通过量化断层合成的价值来寻求推荐乳房活检的最佳阈值。
Proc SPIE Int Soc Opt Eng. 2014 Mar 11;9037:90370U. doi: 10.1117/12.2042905.
6
Breast cancer risk assessment using genetic variants and risk factors in a Singapore Chinese population.利用基因变异和风险因素对新加坡华裔人群进行乳腺癌风险评估。
Breast Cancer Res. 2014 Jun 18;16(3):R64. doi: 10.1186/bcr3678.
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Net reclassification improvement: computation, interpretation, and controversies: a literature review and clinician's guide.净重新分类改善:计算、解释和争议:文献综述及临床医生指南。
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8
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Behind the numbers: Decoding molecular phenotypes with radiogenomics--guiding principles and technical considerations.数字背后:用放射基因组学解码分子表型——指导原则与技术考量
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10
On the assessment of the added value of new predictive biomarkers.关于新预测生物标志物的附加值评估。
BMC Med Res Methodol. 2013 Jul 29;13:98. doi: 10.1186/1471-2288-13-98.

开发一个效用决策框架以评估乳腺癌风险估计中的预测模型。

Developing a utility decision framework to evaluate predictive models in breast cancer risk estimation.

作者信息

Wu Yirong, Abbey Craig K, Chen Xianqiao, Liu Jie, Page David C, Alagoz Oguzhan, Peissig Peggy, Onitilo Adedayo A, Burnside Elizabeth S

机构信息

University of Wisconsin-Madison , Department of Radiology, 600 Highland Avenue, Madison, Wisconsin 53792, United States.

University of California-Santa Barbara , Department of Psychological and Brain Sciences, 251 UCEN Road, Santa Barbara, California 93106, United States.

出版信息

J Med Imaging (Bellingham). 2015 Oct;2(4):041005. doi: 10.1117/1.JMI.2.4.041005. Epub 2015 Aug 17.

DOI:10.1117/1.JMI.2.4.041005
PMID:26835489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4718446/
Abstract

Combining imaging and genetic information to predict disease presence and progression is being codified into an emerging discipline called "radiogenomics." Optimal evaluation methodologies for radiogenomics have not been well established. We aim to develop a decision framework based on utility analysis to assess predictive models for breast cancer diagnosis. We garnered Gail risk factors, single nucleotide polymorphisms (SNPs), and mammographic features from a retrospective case-control study. We constructed three logistic regression models built on different sets of predictive features: (1) Gail, (2) Gail + Mammo, and (3) Gail + Mammo + SNP. Then we generated receiver operating characteristic (ROC) curves for three models. After we assigned utility values for each category of outcomes (true negatives, false positives, false negatives, and true positives), we pursued optimal operating points on ROC curves to achieve maximum expected utility of breast cancer diagnosis. We performed McNemar's test based on threshold levels at optimal operating points, and found that SNPs and mammographic features played a significant role in breast cancer risk estimation. Our study comprising utility analysis and McNemar's test provides a decision framework to evaluate predictive models in breast cancer risk estimation.

摘要

将影像学和基因信息相结合以预测疾病的存在和进展,正被编纂成一门名为“放射基因组学”的新兴学科。放射基因组学的最佳评估方法尚未完全确立。我们旨在基于效用分析开发一个决策框架,以评估乳腺癌诊断的预测模型。我们从一项回顾性病例对照研究中收集了盖尔风险因素、单核苷酸多态性(SNP)和乳房X线摄影特征。我们构建了三个基于不同预测特征集的逻辑回归模型:(1)盖尔模型,(2)盖尔+乳房X线摄影模型,以及(3)盖尔+乳房X线摄影+SNP模型。然后我们生成了这三个模型的受试者工作特征(ROC)曲线。在为每类结果(真阴性、假阳性、假阴性和真阳性)分配效用值后,我们在ROC曲线上寻找最佳操作点,以实现乳腺癌诊断的最大预期效用。我们基于最佳操作点的阈值水平进行了麦克尼马尔检验,发现SNP和乳房X线摄影特征在乳腺癌风险评估中发挥了重要作用。我们包含效用分析和麦克尼马尔检验的研究提供了一个决策框架,用于评估乳腺癌风险评估中的预测模型。