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本文引用的文献

1
A Comprehensive Model of Colorectal Cancer by Risk Factor Status and Subsite Using Data From the Nurses' Health Study.一项利用护士健康研究数据,基于风险因素状况和亚部位的结直肠癌综合模型。
Am J Epidemiol. 2017 Feb 1;185(3):224-237. doi: 10.1093/aje/kww183.
2
Cancer Statistics, 2017.《2017 年癌症统计》
CA Cancer J Clin. 2017 Jan;67(1):7-30. doi: 10.3322/caac.21387. Epub 2017 Jan 5.
3
The American Cancer Society challenge goal to reduce US cancer mortality by 50% between 1990 and 2015: Results and reflections.美国癌症协会挑战目标:1990 年至 2015 年美国癌症死亡率降低 50%:结果与反思。
CA Cancer J Clin. 2016 Sep;66(5):359-69. doi: 10.3322/caac.21348. Epub 2016 May 13.
4
A Prospective Analysis of Meat Mutagens and Colorectal Cancer in the Nurses' Health Study and Health Professionals Follow-up Study.护士健康研究和卫生专业人员随访研究中肉类诱变剂与结直肠癌的前瞻性分析。
Environ Health Perspect. 2016 Oct;124(10):1529-1536. doi: 10.1289/EHP238. Epub 2016 Apr 22.
5
Risk Prediction Models for Colorectal Cancer: A Systematic Review.结直肠癌风险预测模型:一项系统综述
Cancer Prev Res (Phila). 2016 Jan;9(1):13-26. doi: 10.1158/1940-6207.CAPR-15-0274. Epub 2015 Oct 13.
6
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。
Ann Intern Med. 2014 Jan 21;160(2):122-31. doi: 10.7326/M13-1522.
7
Validation of Rosner-Colditz breast cancer incidence model using an independent data set, the California Teachers Study.利用独立数据集加利福尼亚教师研究对 Rosner-Colditz 乳腺癌发病率模型进行验证。
Breast Cancer Res Treat. 2013 Nov;142(1):187-202. doi: 10.1007/s10549-013-2719-3. Epub 2013 Oct 26.
8
Against quantiles: categorization of continuous variables in epidemiologic research, and its discontents.逆分位数法:流行病学研究中连续变量的分类及其不满。
BMC Med Res Methodol. 2012 Feb 29;12:21. doi: 10.1186/1471-2288-12-21.
9
Folate intake and risk of colorectal cancer and adenoma: modification by time.叶酸摄入与结直肠癌和腺瘤风险:时间的影响。
Am J Clin Nutr. 2011 Apr;93(4):817-25. doi: 10.3945/ajcn.110.007781. Epub 2011 Jan 26.
10
Extensions of net reclassification improvement calculations to measure usefulness of new biomarkers.将净重新分类改进计算扩展到测量新生物标志物的有用性。
Stat Med. 2011 Jan 15;30(1):11-21. doi: 10.1002/sim.4085. Epub 2010 Nov 5.

基于短分类生活方式暴露的结肠癌风险预测工具与使用连续测量的模型的性能比较。

Comparison of Performance Between a Short Categorized Lifestyle Exposure-based Colon Cancer Risk Prediction Tool and a Model Using Continuous Measures.

机构信息

Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, Missouri.

Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital, St. Louis, Missouri.

出版信息

Cancer Prev Res (Phila). 2018 Dec;11(12):841-848. doi: 10.1158/1940-6207.CAPR-18-0196. Epub 2018 Nov 16.

DOI:10.1158/1940-6207.CAPR-18-0196
PMID:30446519
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6295201/
Abstract

Risk prediction models that estimate an individual's risk of developing colon cancer could be used for a variety of clinical and public health interventions, including offering high-risk individuals enhanced screening or lifestyle interventions. However, if risk prediction models are to be translated into actual clinical and public health practice, they must not only be valid and reliable, but also be easy to use. One way of accomplishing this might be to simplify the information that users of risk prediction tools have to enter, but it is critical to ensure no resulting detrimental effects on model performance. We compared the performance of a simplified, largely categorized exposure-based colon cancer risk model against a more complex, largely continuous exposure-based risk model using two prospective cohorts. Using data from the Nurses' Health Study and the Health Professionals Follow-up Study we included 816 incident colon cancer cases in women and 412 in men. The discrimination of models was not significantly different comparing a categorized risk prediction model with a continuous prediction model in women (c-statistic 0.600 vs. 0.609, = 0.07) and men (c-statistic 0.622 vs. 0.618, = 0.60). Both models had good calibration in men [observed case count/expected case count (O/E) = 1.05, > 0.05] but not in women (O/E = 1.19, < 0.01). Risk reclassification was slightly improved using categorized predictors in men [net reclassification index (NRI) = 0.041] and slightly worsened in women (NRI = -0.065). Categorical assessment of predictor variables may facilitate use of risk assessment tools in the general population without significant loss of performance.

摘要

风险预测模型可以用来估计个体患结肠癌的风险,这些模型可用于多种临床和公共卫生干预措施,包括为高风险个体提供增强筛查或生活方式干预。然而,如果要将风险预测模型转化为实际的临床和公共卫生实践,它们不仅必须有效和可靠,而且还必须易于使用。实现这一目标的一种方法可能是简化风险预测工具使用者必须输入的信息,但必须确保这不会对模型性能产生不利影响。我们比较了简化的、主要基于分类的结肠癌风险模型和更复杂的、主要基于连续的暴露风险模型的性能,使用了两个前瞻性队列。利用来自护士健康研究和卫生专业人员随访研究的数据,我们纳入了 816 例女性和 412 例男性的结肠癌发病病例。在女性中,分类风险预测模型与连续预测模型的区分度没有显著差异(c 统计量 0.600 与 0.609, = 0.07),在男性中也没有显著差异(c 统计量 0.622 与 0.618, = 0.60)。两个模型在男性中都具有良好的校准度[观察病例数/预期病例数(O/E)= 1.05, > 0.05],但在女性中则不然(O/E = 1.19, < 0.01)。使用分类预测因子可略微改善男性的风险再分类[净重新分类指数(NRI)= 0.041],但会略微恶化女性的风险再分类(NRI = -0.065)。对预测变量的分类评估可能会促进风险评估工具在普通人群中的使用,而不会显著降低性能。