Department of Medicine, Stanford University School of Medicine, Stanford, California.
Department of Medicine, Stanford University School of Medicine, Stanford, California; Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, California.
Clin Gastroenterol Hepatol. 2014 Oct;12(10):1624-34.e1. doi: 10.1016/j.cgh.2014.01.042. Epub 2014 Feb 15.
BACKGROUND & AIMS: A valid risk prediction model for colorectal neoplasia would allow patients to be screened for colorectal cancer (CRC) on the basis of risk. We performed a systematic review of studies reporting risk prediction models for colorectal neoplasia.
We conducted a systematic search of MEDLINE, Scopus, and Cochrane Library databases from January 1990 through March 2013 and of references in identified studies. Case-control, cohort, and cross-sectional studies that developed or attempted to validate a model to predict risk of colorectal neoplasia were included. Two reviewers independently extracted data and assessed model quality. Model quality was considered to be good for studies that included external validation, fair for studies that included internal validation, and poor for studies with neither.
Nine studies developed a new prediction model, and 2 tested existing models. The models varied with regard to population, predictors, risk tiers, outcomes (CRC or advanced neoplasia), and range of predicted risk. Several included age, sex, smoking, a measure of obesity, and/or family history of CRC among the predictors. Quality was good for 6 models, fair for 2 models, and poor for 1 model. The tier with the largest population fraction (low, intermediate, or high risk) depended on the model. For most models that defined risk tiers, the risk difference between the highest and lowest tier ranged from 2-fold to 4-fold. Two models reached the 0.70 threshold for the C statistic, typically considered to indicate good discriminatory power.
Most current colorectal neoplasia risk prediction models have relatively weak discriminatory power and have not demonstrated generalizability. It remains to be determined how risk prediction models could inform CRC screening strategies.
有效的结直肠肿瘤风险预测模型可以使患者能够根据风险接受结直肠癌(CRC)筛查。我们对报道结直肠肿瘤风险预测模型的研究进行了系统评价。
我们对 1990 年 1 月至 2013 年 3 月 MEDLINE、Scopus 和 Cochrane 图书馆数据库以及已确定研究的参考文献进行了系统检索。纳入了开发或试图验证用于预测结直肠肿瘤风险的模型的病例对照、队列和横断面研究。两名审查员独立提取数据并评估模型质量。考虑到外部验证的研究为质量好,考虑到内部验证的研究为质量一般,既没有外部验证也没有内部验证的研究为质量差。
9 项研究开发了新的预测模型,2 项研究检验了现有的模型。这些模型在人群、预测因素、风险分层、结局(CRC 或高级别腺瘤)和预测风险范围方面存在差异。一些研究包括年龄、性别、吸烟、肥胖指标和/或 CRC 家族史作为预测因素。6 个模型质量好,2 个模型质量一般,1 个模型质量差。人群比例最大的分层(低、中或高风险)取决于模型。对于大多数定义风险分层的模型,最高分层与最低分层之间的风险差异为 2 倍至 4 倍。有两个模型达到了 C 统计量的 0.70 阈值,通常认为该阈值具有良好的区分能力。
大多数现有的结直肠肿瘤风险预测模型的区分能力相对较弱,尚未证明具有通用性。风险预测模型如何为 CRC 筛查策略提供信息仍有待确定。