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LLP风险模型:一种用于肺癌的个体风险预测模型。

The LLP risk model: an individual risk prediction model for lung cancer.

作者信息

Cassidy A, Myles J P, van Tongeren M, Page R D, Liloglou T, Duffy S W, Field J K

机构信息

Roy Castle Lung Cancer Research Programme, University of Liverpool Cancer Research Centre, Liverpool, L3 9TA, UK.

出版信息

Br J Cancer. 2008 Jan 29;98(2):270-6. doi: 10.1038/sj.bjc.6604158. Epub 2007 Dec 18.

DOI:10.1038/sj.bjc.6604158
PMID:18087271
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2361453/
Abstract

Using a model-based approach, we estimated the probability that an individual, with a specified combination of risk factors, would develop lung cancer within a 5-year period. Data from 579 lung cancer cases and 1157 age- and sex-matched population-based controls were available for this analysis. Significant risk factors were fitted into multivariate conditional logistic regression models. The final multivariate model was combined with age-standardised lung cancer incidence data to calculate absolute risk estimates. Combinations of lifestyle risk factors were modelled to create risk profiles. For example, a 77-year-old male non-smoker, with a family history of lung cancer (early onset) and occupational exposure to asbestos has an absolute risk of 3.17% (95% CI, 1.67-5.95). Choosing a 2.5% cutoff to trigger increased surveillance, gave a sensitivity of 0.62 and specificity of 0.70, while a 6.0% cutoff gave a sensitivity of 0.34 and specificity of 0.90. A 10-fold cross validation produced an AUC statistic of 0.70, indicating good discrimination.If independent validation studies confirm these results, the LLP risk models' application as the first stage in an early detection strategy is a logical evolution in patient care.

摘要

我们采用基于模型的方法,估计了具有特定风险因素组合的个体在5年内患肺癌的概率。本分析使用了来自579例肺癌病例以及1157名年龄和性别匹配的基于人群的对照的数据。将显著的风险因素纳入多变量条件逻辑回归模型。最终的多变量模型与年龄标准化的肺癌发病率数据相结合,以计算绝对风险估计值。对生活方式风险因素的组合进行建模以创建风险概况。例如,一名77岁的男性非吸烟者,有肺癌家族史(早发)且职业接触过石棉,其绝对风险为3.17%(95%置信区间,1.67 - 5.95)。选择2.5%的临界值以启动强化监测,灵敏度为0.62,特异度为0.70,而6.0%的临界值灵敏度为0.34,特异度为0.90。10倍交叉验证产生的AUC统计量为0.70,表明具有良好的区分度。如果独立验证研究证实这些结果,那么肺癌风险模型作为早期检测策略的第一阶段应用将是患者护理方面的合理进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd6a/2361453/d36f03ad4db4/6604158f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd6a/2361453/d36f03ad4db4/6604158f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd6a/2361453/d36f03ad4db4/6604158f1.jpg

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