摘要PR17:综合预测结直肠癌风险,为个性化筛查和干预提供信息

Jihyoun Jeon, S. Berndt, H. Brenner, P. Campbell, A. Chan, J. Chang-Claude, Mengmeng Du, G. Giles, Jian Gong, S. Gruber, T. Harrison, M. Hoffmeister, L. LeMarchand, Li Li, J. Potter, G. Rennert, R. Schoen, M. Slattery, E. White, M. Woods, U. Peters, L. Hsu
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Our models also estimate absolute risk of developing CRC given various risk profiles, and provide recommended ages for the first endoscopic screening exam. Results: Both the E-score and the G-score are independent predictors of CRC risk, and models that incorporate both scores improve the discriminatory accuracy significantly compared to family history-only models. Compared to the model that includes only family history, the E-score significantly improves the discriminatory accuracy for both men (AUC = 0.62 vs. 0.53, p-value Conclusions: Our risk prediction models incorporating both comprehensive environmental and lifestyle risk factors, and known CRC common genetic variants provide more accurate estimation of CRC risk. These models will be useful for recommending individually tailored screening and intervention strategies to prevent this common cancer. This abstract is also being presented as Poster B17. Citation Format: Jihyoun Jeon, Sonja I. Berndt, Hermann Brenner, Peter T. 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引用次数: 0

摘要

背景与目的:通过筛查早期发现结直肠癌(CRC)是最容易预防和治疗的癌症之一。目前的CRC筛查指南建议仅根据年龄、家族史和以前的筛查结果进行检查。然而,多种环境和生活方式风险因素已被确定或怀疑为结直肠癌的风险因素,以及许多常见的遗传易感位点。利用这些信息更好地将个体划分为低危组和高危组,以优化和个性化筛查和干预建议是至关重要的。方法:使用来自两个大型联盟(8421例结直肠癌病例和9767例对照)的数据:结直肠癌遗传与流行病学联盟(GECCO)和结直肠癌跨学科研究(correct),我们基于家族史、环境和生活方式风险因素以及通过全基因组关联研究确定的已知结直肠癌易感位点,建立了男性和女性的风险预测模型。我们构建了一个环境风险评分(E-score),作为19个已知或潜在的结直肠癌环境和生活方式风险因素的加权和,其权重来自多变量logistic回归分析。同样,我们还使用64种与结直肠癌风险相关的常见变异构建了遗传风险评分(G-score)。我们通过计算接收者工作特征曲线(AUC)下的面积来评估风险预测模型的区分准确性,并使用训练数据集纠正潜在的高估。我们的模型还估计了在各种风险情况下发生CRC的绝对风险,并提供了首次内镜筛查检查的推荐年龄。结果:E-score和G-score都是结直肠癌风险的独立预测因子,与仅包含家族史的模型相比,包含这两种评分的模型显著提高了区分准确性。与仅包含家族史的模型相比,E-score显著提高了两种男性的区分准确性(AUC = 0.62 vs. 0.53, p值)。结论:我们的风险预测模型结合了综合环境和生活方式风险因素,以及已知的CRC常见遗传变异,可以更准确地估计CRC风险。这些模型将有助于推荐个体化筛查和干预策略,以预防这种常见癌症。此摘要也以海报B17的形式呈现。引文格式:Jihyoun Jeon, Sonja I. Berndt, Hermann Brenner, Peter T. Campbell, Andrew T. Chan, Jenny Chang-Claude, Du Mengmeng, Graham Giles, Jian Gong, Stephen B. Gruber, Tabitha . Harrison, Michael Hoffmeister, Loic LeMarchand, Li Li, John D. Potter, Gad Rennert, Robert E. Schoen, Martha L. Slattery, Emily White, Michael O. Woods, Ulrike Peters, Li Hsu。综合结肠直肠癌风险预测为个性化筛查和干预提供信息。[摘要]。摘自:AACR特别会议论文集:改进癌症风险预测以预防和早期发现;2016年11月16日至19日;费城(PA): AACR;Cancer epidemiology Biomarkers pre2017;26(5增刊):摘要nr PR17。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abstract PR17: Comprehensive colorectal cancer risk prediction to inform personalized screening and intervention
Background and Aims: Colorectal cancer (CRC) is one of the most preventable and treatable cancers when detected early via screening. The current screening guidelines for CRC recommend exams only based on age, family history, and previous screening results. Multiple environmental and lifestyle risk factors, however, have been established or suspected for CRC, as have many common genetic susceptibility loci. It is critical to utilize this information to better stratify individuals into low- and high-risk groups for optimized and personalized screening and intervention recommendations. Methods: Using data from two large consortia (8421 CRC cases and 9767 controls): the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO) and the Colorectal Transdisciplinary study (CORECT), we developed risk prediction models for men and women based on family history, environmental and lifestyle risk factors, and known CRC susceptibility loci identified through genome-wide association studies. We constructed an environmental risk score (E-score) as a weighted sum of 19 established or potential environmental and lifestyle risk factors for CRC with weights obtained from a multivariate logistic regression analysis. Similarly, we also constructed a genetic risk score (G-score) using 64 common variants associated with CRC risk. We evaluated the discriminatory accuracy of risk prediction models by calculating the area under the Receiver Operating Characteristic curve (AUC), correcting for potential overestimating by using the training data set. Our models also estimate absolute risk of developing CRC given various risk profiles, and provide recommended ages for the first endoscopic screening exam. Results: Both the E-score and the G-score are independent predictors of CRC risk, and models that incorporate both scores improve the discriminatory accuracy significantly compared to family history-only models. Compared to the model that includes only family history, the E-score significantly improves the discriminatory accuracy for both men (AUC = 0.62 vs. 0.53, p-value Conclusions: Our risk prediction models incorporating both comprehensive environmental and lifestyle risk factors, and known CRC common genetic variants provide more accurate estimation of CRC risk. These models will be useful for recommending individually tailored screening and intervention strategies to prevent this common cancer. This abstract is also being presented as Poster B17. Citation Format: Jihyoun Jeon, Sonja I. Berndt, Hermann Brenner, Peter T. Campbell, Andrew T. Chan, Jenny Chang-Claude, Mengmeng Du, Graham Giles, Jian Gong, Stephen B. Gruber, Tabitha A. Harrison, Michael Hoffmeister, Loic LeMarchand, Li Li, John D. Potter, Gad Rennert, Robert E. Schoen, Martha L. Slattery, Emily White, Michael O. Woods, Ulrike Peters, Li Hsu. Comprehensive colorectal cancer risk prediction to inform personalized screening and intervention. [abstract]. In: Proceedings of the AACR Special Conference: Improving Cancer Risk Prediction for Prevention and Early Detection; Nov 16-19, 2016; Orlando, FL. Philadelphia (PA): AACR; Cancer Epidemiol Biomarkers Prev 2017;26(5 Suppl):Abstract nr PR17.
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