From Algorithms to Clinical Utility: A Systematic Review of Individualized Risk Prediction Models for Colorectal Cancer

被引:4
作者
Herrera, Deborah Jael [1 ]
van de Veerdonk, Wessel [1 ,2 ]
Seibert, Daiane Maria [3 ]
Boke, Moges Muluneh [1 ]
Gutierrez-Ortiz, Claudia [1 ]
Yimer, Nigus Bililign [1 ]
Feyen, Karen [3 ]
Ferrari, Allegra [1 ,4 ]
Van Hal, Guido [1 ]
机构
[1] Univ Antwerp, Fac Med & Hlth Sci, Family Med & Populat Hlth Dept FAMPOP, B-2610 Antwerp, Belgium
[2] Thomas More Univ Appl Sci, Ctr Expertise Care & Well Being, Campus Zandpoortvest, B-2800 Mechelen, Belgium
[3] Thomas More Univ Appl Sci, Ctr Expertise Design & Technol, Campus De Nayer, B-2800 Mechelen, Belgium
[4] Univ Genoa, Dept Hlth Sci DISSAL, Via Pastore 1, I-16138 Genoa, Italy
关键词
risk prediction; risk scores; colorectal cancer; advanced neoplasia; risk factors; model performance; clinical utility; FECAL HEMOGLOBIN CONCENTRATION; SCORING SYSTEM; NEOPLASM RISK; VALIDATION; TOOL; DERIVATION; APPLICABILITY; COLONOSCOPY; ADENOMA; PROBAST;
D O I
10.3390/gidisord5040045
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Individualized risk prediction models for colorectal cancer (CRC) play a pivotal role in shaping risk-based screening approaches, garnering attention for use in informed decision making by patients and clinicians. While the incorporation of new predictors and the development of advanced yet complex prediction models can enhance model performance, their practical implementation in clinical settings remains challenging. This systematic review assessed individualized CRC risk prediction models for their validity and potential clinical utility. Utilizing the Cochrane Collaboration methods and PROBAST tool, we conducted comprehensive searches across key databases and risk of bias assessment, respectively. Out of 41 studies included evaluating 44 risk prediction models, 12 conventional and 3 composite models underwent external validation. All risk models exhibited varying discriminatory accuracy, with the area under the curve (AUCs) ranging from 0.57 to 0.90. However, most studies showed an unclear or high risk of bias, with concerns about applicability. Of the five models with promising clinical utility, only two underwent external validation and one employed a decision curve analysis. These models demonstrated a discriminating and well-calibrated performance. While high-performing CRC risk prediction models exist, a need for transparent reporting of performance metrics and their clinical utility persists. Further research on this area is needed to facilitate the integration of these models into clinical practice, particularly in CRC screening.
引用
收藏
页码:549 / 579
页数:31
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