Carr Rosalie A, Yip-Schneider Michele T, Dolejs Scott, Hancock Bradley A, Wu Huangbing, Radovich Milan, Schmidt Max C
Department of Surgery, Indiana University School of Medicine, Indianapolis, IN Department of Biochemistry/Molecular Biology, Indiana University School of Medicine, Indianapolis, IN Walther Oncology Center, Indianapolis, IN Indiana University Cancer Center, Indianapolis, IN Indiana University Health Pancreatic Cyst and Cancer Early Detection Center, Indianapolis, IN.
J Am Coll Surg. 2017 Jul 1;225(1):93-100. doi: 10.1016/j.jamcollsurg.2017.05.003.
Accurate differentiation of pancreatic cystic lesions is important for early detection and prevention of pancreatic cancer, as well as avoidance of unnecessary surgical intervention. Serous cystic neoplasms (SCNs) have no malignant potential, but can mimic the following premalignant mucinous cystic lesions: mucinous cystic neoplasm and intraductal papillary mucinous neoplasm (IPMN). We recently identified vascular endothelial growth factor (VEGF)-A as a novel pancreatic fluid biomarker for SCN. We hypothesize that combining cyst fluid CEA with VEGF-A will improve the diagnostic accuracy of VEGF-A. Pancreatic cyst/duct fluid was collected from consenting patients undergoing surgical cyst resection with corresponding pathologic diagnoses. Pancreatic fluid VEGF-A and CEA levels were detected by ELISA. One hundred and forty-nine patients with pancreatic cystic lesions met inclusion criteria. Pathologic diagnoses included pseudocyst (n = 14), SCN (n = 26), mucinous cystic neoplasm (n = 40), low-/moderate-grade IPMN (n = 34), high-grade IPMN (n = 20), invasive IPMN (n = 10), and solid pseudopapillary neoplasm (n = 5). Vascular endothelial growth factor A was significantly elevated in SCN cyst fluid compared with all other diagnoses (p < 0.001). With a threshold of >5,000 pg/mL, VEGF-A alone has 100% sensitivity and 83.7% specificity to distinguish SCNs from other cystic lesions. With a threshold of ≤10 ng/mL, CEA alone identifies SCN with 95.5% sensitivity and 81.5% specificity. Sensitivity and specificity of the VEGF-A/CEA combination are 95.5% and 100%, respectively. The c-statistic increased from 0.98 to 0.99 in the receiver operating characteristic analysis when CEA was added to VEGF-A alone. Although VEGF-A alone is a highly accurate test for SCN, the combination of VEGF-A with CEA approaches the gold standard for pathologic diagnosis, importantly avoiding false positives. Patients with a positive test indicating benign SCN can be spared a high-risk surgical pancreatic resection.
准确鉴别胰腺囊性病变对于胰腺癌的早期发现和预防,以及避免不必要的手术干预至关重要。浆液性囊性肿瘤(SCNs)无恶性潜能,但可酷似以下癌前黏液性囊性病变:黏液性囊性肿瘤和导管内乳头状黏液性肿瘤(IPMN)。我们最近鉴定出血管内皮生长因子(VEGF)-A是一种用于SCN的新型胰腺液生物标志物。我们假设将囊液癌胚抗原(CEA)与VEGF-A联合使用将提高VEGF-A的诊断准确性。从接受手术性囊肿切除并伴有相应病理诊断的知情患者中收集胰腺囊肿/导管液。通过酶联免疫吸附测定(ELISA)检测胰腺液VEGF-A和CEA水平。149例胰腺囊性病变患者符合纳入标准。病理诊断包括假性囊肿(n = 14)、SCN(n = 26)、黏液性囊性肿瘤(n = 40)、低/中度IPMN(n = 34)、高级别IPMN(n = 20)、浸润性IPMN(n = 10)和实性假乳头状肿瘤(n = 5)。与所有其他诊断相比,SCN囊液中的血管内皮生长因子A显著升高(p < 0.001)。以>5,000 pg/mL为阈值,单独的VEGF-A区分SCN与其他囊性病变的敏感性为100%,特异性为83.7%。以≤10 ng/mL为阈值,单独的CEA识别SCN的敏感性为95.5%,特异性为81.5%。VEGF-A/CEA联合检测的敏感性和特异性分别为95.5%和100%。在接受者操作特征分析中,当单独的VEGF-A加入CEA时,c统计量从0.98增加到0.99。尽管单独的VEGF-A对SCN是一种高度准确的检测方法,但VEGF-A与CEA联合使用接近病理诊断的金标准,重要的是避免假阳性。检测结果呈阳性表明为良性SCN的患者可避免高风险的胰腺手术切除。