Park Joo Kyung, Paik Woo Hyun, Song Byeong Jun, Ryu Ji Kon, Kim Min A, Park Jin Myung, Lee Sang Hyub, Kim Yong-Tae
Department of Medicine, Division of Gastroenterology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Internal Medicine, Inje University Ilsan Paik Hospital, Goyang, Korea.
Oncotarget. 2017 Mar 11;8(38):64440-64448. doi: 10.18632/oncotarget.16135. eCollection 2017 Sep 8.
One of the major genetic alterations in pancreatic ductal adenocarcinoma (PDAC) is the point mutation of K-ras gene. Plectin-1 was also recently identified as PDAC specific biomarker. The aim of this study was to investigate the improvement of diagnostic accuracy of endoscopic ultrasound-guided fine needle aspiration (EUS-FNA) by using additional K-ras mutation analysis and Plectin-1 staining in patients with pancreatic mass.
A total of 85 study patients with pancreatic mass underwent EUS-FNA and the final diagnoses were as follows; PDACs: 70 patients, pancreas neuroendocrine tumor: 4, metastasis to pancreas: 5, autoimmune pancreatitis: 3, chronic pancreatitis: 1, tuberculous lymphadenitis: 1, pseudocyst: 1.
Sensitivity, specificity and accuracy of pathologic diagnosis in EUS-FNA specimen were 81%, 80% and 79% accordingly. When we combine K-ras gene mutation analysis with histological assessment, we could get the following results for sensitivity, specificity and accuracy; cytology and K-ras mutation analysis: 93%, 87%, and 92%, cytology, K-ras mutation analysis, and Plectin-1 staining: 96%, 93%, and 95%.
Triple combinations of the techniques; cytology, K-ras gene mutation analysis, Plectin-1 staining could increase accuracy in diagnosis of PDACs. Further investigation of using minimal specimens from EUS-FNA may give us insight to understand the biological behavior of PDAC.
胰腺导管腺癌(PDAC)的主要基因改变之一是K-ras基因的点突变。Plectin-1最近也被确定为PDAC特异性生物标志物。本研究的目的是通过对胰腺肿块患者进行额外的K-ras突变分析和Plectin-1染色,探讨提高内镜超声引导下细针穿刺活检(EUS-FNA)诊断准确性的方法。
共有85例胰腺肿块患者接受了EUS-FNA,最终诊断结果如下:PDAC患者70例,胰腺神经内分泌肿瘤4例,胰腺转移瘤5例,自身免疫性胰腺炎3例,慢性胰腺炎1例,结核性淋巴结炎1例,假性囊肿1例。
EUS-FNA标本病理诊断的敏感性、特异性和准确性分别为81%、80%和79%。当我们将K-ras基因突变分析与组织学评估相结合时,敏感性、特异性和准确性结果如下:细胞学检查和K-ras基因突变分析:93%、87%和92%,细胞学检查、K-ras基因突变分析和Plectin-1染色:96%、93%和95%。
细胞学检查、K-ras基因突变分析、Plectin-1染色这三种技术联合应用可提高PDAC的诊断准确性。进一步研究使用EUS-FNA获取的少量标本,可能有助于我们了解PDAC的生物学行为。