Hajibandeh Shahab, Intrator Christina, Carrington-Windo Eliot, James Rhodri, Hughes Ioan, Hajibandeh Shahin, Satyadas Thomas
Department of General Surgery, University Hospital of Wales, Cardiff & Vale NHS Trust, Cardiff CF14 4XW, UK.
Department of Hepatobiliary and Pancreatic Surgery, Manchester Royal Infirmary Hospital, Manchester M13 9WL, UK.
Biomedicines. 2023 Nov 14;11(11):3040. doi: 10.3390/biomedicines11113040.
To investigate the performance of the END-PAC model in predicting pancreatic cancer risk in individuals with new-onset diabetes (NOD).
The PRISMA statement standards were followed to conduct a systematic review. All studies investigating the performance of the END-PAC model in predicting pancreatic cancer risk in individuals with NOD were included. Two-by-two tables, coupled forest plots and summary receiver operating characteristic plots were constructed using the number of true positives, false negatives, true negatives and false positives. Diagnostic random effects models were used to estimate summary sensitivity and specificity points.
A total of 26,752 individuals from four studies were included. The median follow-up was 3 years and the pooled risk of pancreatic cancer was 0.8% (95% CI 0.6-1.0%). END-PAC score ≥ 3, which classifies the patients as high risk, was associated with better predictive performance (sensitivity: 55.8% (43.9-67%); specificity: 82.0% (76.4-86.5%)) in comparison with END-PAC score 1-2 (sensitivity: 22.2% (16.6-29.2%); specificity: 69.9% (67.3-72.4%)) and END-PAC score < 1 (sensitivity: 18.0% (12.8-24.6%); specificity: 50.9% (48.6-53.2%)) which classify the patients as intermediate and low risk, respectively. The evidence quality was judged to be moderate to high.
END-PAC is a promising model for predicting pancreatic cancer risk in individuals with NOD. The score ≥3 should be considered as optimum cut-off value. More studies are needed to assess whether it could improve early pancreatic cancer detection rate, pancreatic cancer re-section rate, and pancreatic cancer treatment outcomes.
研究END-PAC模型在预测新发糖尿病(NOD)个体患胰腺癌风险方面的性能。
遵循PRISMA声明标准进行系统评价。纳入所有研究END-PAC模型在预测NOD个体患胰腺癌风险方面性能的研究。使用真阳性、假阴性、真阴性和假阳性的数量构建二乘二列联表、森林图和汇总受试者工作特征图。采用诊断随机效应模型估计汇总敏感性和特异性点。
共纳入四项研究中的26752名个体。中位随访时间为3年,胰腺癌的合并风险为0.8%(95%CI 0.6-1.0%)。将患者分类为高风险的END-PAC评分≥3与更好的预测性能相关(敏感性:55.8%(43.9-67%);特异性:82.0%(76.4-86.5%)),相比之下,将患者分别分类为中风险和低风险的END-PAC评分1-2(敏感性:22.2%(16.6-29.2%);特异性:69.9%(67.3-72.4%))和END-PAC评分<1(敏感性:18.0%(12.8-24.6%);特异性:50.9%(48.6-53.2%))。证据质量被判定为中等到高。
END-PAC是预测NOD个体患胰腺癌风险的一个有前景的模型。评分≥3应被视为最佳临界值。需要更多研究来评估它是否能提高早期胰腺癌检出率、胰腺癌再切除率和胰腺癌治疗效果。