Department of Surgery, University Hospital of Wales, Cardiff, Wales, UK.
Hepatobiliary Pancreat Dis Int. 2009 Dec;8(6):620-6.
CA19-9 is a carbohydrate tumor-associated antigen which is frequently upregulated in pancreatobiliary neoplasia. However, it may also be elevated in patients with jaundice in the absence of a tumor due to biliary obstruction, and in other non-hepato-pancreatico-biliary conditions. This study aimed to evaluate whether CA19-9 levels could accurately differentiate between benign and malignant pancreatobiliary disease.
All patients referred to a single surgeon for investigation of pancreaticobiliary disease in 2003 in whom a firm diagnosis had been established were included. For malignant disease, a histological diagnosis was required but for benign disease a firm radiological diagnosis was deemed adequate. The patients were divided into 4 categories: pancreatic adenocarcinoma (PCa); cholangiocarcinoma (CCa); chronic pancreatitis (CP) and biliary calculous disease (Calc). Bilirubin and alkaline phosphatase levels corresponding to the point of assessment of CA19-9 were also noted.
Final diagnoses were made of pancreatic adenocarcinoma (PCa, n=73), cholangiocarcinoma (CCa, n=19), ampullary carcinoma (Amp, n=7), neuroendocrine carcinoma (Neu, n=4), duodenal carcinoma (Duo, n=3), chronic pancreatitis (CP, n=115), and biliary calculous disease (Calc, n=27). Median CA19-9 levels (U/ml) were: PCa, 653; CCa, 408; Duo, 403; Calc, 27; CP, 19; Neu, 10.5; Amp, 8 (reference range: 0-37). The CA19-9 levels were significantly greater for malignant than for benign disease, could differentiate PCa from CCa/Duo, and were significantly higher in unresectable than in resectable PCa. The sensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) for CA19-9 were 84.9%, 69.7%, 67.7% and 86.1%, respectively. A ROC analysis provided an area under the curve for CA19-9 of 0.871 (0.820-0.922), giving an optimal CA19-9 of 70.5 U/ml for differentiating benign from malignant pathology. Using this cut-off, the sensitivity was 82.1%, while specificity, PPV and NPV improved to 85.9%, 81.3% and 86.5%, respectively. When standard radiology was included (US/CT/MRCP) in the decision process, the results improved to 97.2%, 88.7%, 86.6%, and 97.7%. For benign disease, the CA19-9 correlated directly with the serum bilirubin, but for malignant disease, CA19-9 levels were elevated independent of the bilirubin level.
CA19-9 is useful in the differentiation of pancreatobiliary disease and when using an optimized cut-off and combining with routine radiology, the diagnostic yield is improved significantly, thus stressing the importance of a multi-disciplinary approach to pancreatobiliary disease.
CA19-9 是一种碳水化合物肿瘤相关抗原,在胰胆管肿瘤中常被上调。然而,在没有肿瘤的情况下,由于胆道梗阻,黄疸患者的 CA19-9 也可能升高,并且在其他非肝胰胆疾病中也可能升高。本研究旨在评估 CA19-9 水平是否能准确地区分良恶性胰胆管疾病。
纳入了 2003 年由一位外科医生诊治的所有胰胆管疾病患者,这些患者均已明确诊断。对于恶性疾病,需要组织学诊断,但对于良性疾病,影像学诊断就足够了。患者分为 4 组:胰腺腺癌(PCa);胆管癌(CCa);慢性胰腺炎(CP)和胆石病(Calc)。还记录了与 CA19-9 评估点相对应的胆红素和碱性磷酸酶水平。
最终诊断为胰腺腺癌(PCa,n=73)、胆管癌(CCa,n=19)、壶腹癌(Amp,n=7)、神经内分泌癌(Neu,n=4)、十二指肠癌(Duo,n=3)、慢性胰腺炎(CP,n=115)和胆石病(Calc,n=27)。CA19-9 中位数(U/ml)分别为:PCa,653;CCa,408;Duo,403;Calc,27;CP,19;Neu,10.5;Amp,8(参考范围:0-37)。恶性疾病的 CA19-9 水平明显高于良性疾病,可将 PCa 与 CCa/Duo 区分开来,不可切除的 PCa 明显高于可切除的 PCa。CA19-9 的敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV)分别为 84.9%、69.7%、67.7%和 86.1%。ROC 分析显示 CA19-9 的曲线下面积为 0.871(0.820-0.922),最佳 CA19-9 截断值为 70.5 U/ml,可区分良性和恶性病理。使用该截断值,敏感性为 82.1%,特异性、PPV 和 NPV 分别提高至 85.9%、81.3%和 86.5%。当将标准影像学(US/CT/MRCP)纳入决策过程时,结果提高至 97.2%、88.7%、86.6%和 97.7%。对于良性疾病,CA19-9 与血清胆红素直接相关,但对于恶性疾病,CA19-9 水平升高与胆红素水平无关。
CA19-9 可用于胰胆管疾病的鉴别,当使用优化的截断值并结合常规影像学检查时,诊断效果显著提高,因此强调了多学科方法治疗胰胆管疾病的重要性。