Saunders Tyler Seyhan, Virpal Pawandeep, Andreou Maria, Parmar Asha, Derksen Christina, Blyuss Oleg, Walter Fiona M, Funston Garth
Centre for Cancer Screening, Prevention and Early Diagnosis, Wolfson Institute of Population Health, Queen Mary University of London, London, United Kingdom.
Cancer Epidemiol Biomarkers Prev. 2025 Aug 1;34(8):1240-1251. doi: 10.1158/1055-9965.EPI-24-1714.
Upper gastrointestinal (UGI) cancers are often detected late. Risk prediction models could facilitate earlier detection by identifying patients at risk for further investigation. We systematically reviewed evidence on UGI diagnostic risk prediction models. A search of MEDLINE, Embase, and CENTRAL was conducted for studies reporting on the development and/or validation of diagnostic risk prediction models for UGI cancers (pancreatic, gastric, esophageal, gallbladder, and/or biliary tract). Studies had to report at least one quantitative measure of model performance to be eligible for inclusion. A total of 82 studies describing 162 UGI risk models were included. Models predicted gallbladder (n = 6), gastric (n = 25), esophageal (n = 34), gastroesophageal (n = 14), and pancreatic (n = 83) cancers. Most models used logistic regression, but machine learning was increasingly used from 2019. In total, 366 unique variables were incorporated across models. Only 33 models were externally validated, with 15 achieving an AUC ≥0.80. This review highlights that several models perform well in predicting UGI cancers on external validation. Future research is needed to compare the best-performing models and assess their clinical utility, acceptability, and cost-effectiveness. Given the significant overlap in at-risk populations and predictors across UGI cancers, there may also be scope to develop UGI "multicancer" models.
上消化道(UGI)癌症往往发现较晚。风险预测模型可通过识别有进一步检查风险的患者来促进早期发现。我们系统回顾了关于UGI诊断风险预测模型的证据。对MEDLINE、Embase和CENTRAL进行了检索,以查找报告UGI癌症(胰腺癌、胃癌、食管癌、胆囊癌和/或胆管癌)诊断风险预测模型开发和/或验证情况的研究。研究必须报告至少一项模型性能的定量指标才有资格纳入。共纳入了82项描述162个UGI风险模型的研究。这些模型预测胆囊癌(n = 6)、胃癌(n = 25)、食管癌(n = 34)、胃食管癌(n = 14)和胰腺癌(n = 83)。大多数模型使用逻辑回归,但从2019年起机器学习的使用越来越多。各模型总共纳入了366个独特变量。只有33个模型进行了外部验证,其中15个模型的曲线下面积(AUC)≥0.80。本综述强调,有几个模型在外部验证中对UGI癌症的预测表现良好。未来需要开展研究来比较表现最佳的模型,并评估其临床实用性、可接受性和成本效益。鉴于UGI癌症的高危人群和预测因素存在显著重叠,开发UGI“多癌”模型可能也具有可行性。