American Gastroenterological Association guidelines are inaccurate in detecting pancreatic cysts with advanced neoplasia: a clinicopathologic study of 225 patients with supporting molecular data

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• 作者：Aatur D. Singhi ; MD ; PhD¹ ; ; Herbert J. Zeh ; MD² ; Randall E. Brand ; MD³ ; Marina N. Nikiforova ; MD¹ ; Jennifer S. Chennat ; MD³ ; Kenneth E. Fasanella ; MD³ ; Asif Khalid ; MD³ ; Georgios I. Papachristou ; MD³ ; Adam Slivka ; MD ; PhD³ ; Melissa Hogg ; MD² ; Kenneth K. Lee ; MD² ; Allan Tsung ; MD² ; Amer H. Zureikat ; MD² ; ³ ; Kevin McGrath ; MD³
• 关键词：AGA ; American Gastroenterological Association ; CEA ; carcinoembryonic antigen ; IPMN ; intraductal papillary mucinous neoplasm ; MCN ; mucinous cystic neoplasm ; MRI ; magnetic resonance imaging ; PanNET ; pancreatic neuroendocrine tumor ; SCA ; serous cystadenoma
• 刊名：Gastrointestinal Endoscopy
• 出版年：2016
• 出版时间：June 2016
• 年：2016
• 卷：83
• 期：6
• 页码：1107-1117.e2
• 全文大小：614 K

文摘

The American Gastroenterological Association (AGA) recently reported evidence-based guidelines for the management of asymptomatic neoplastic pancreatic cysts. These guidelines advocate a higher threshold for surgical resection than prior guidelines and imaging surveillance for a considerable number of patients with pancreatic cysts. The aims of this study were to assess the accuracy of the AGA guidelines in detecting advanced neoplasia and present an alternative approach to pancreatic cysts.

Methods

The study population consisted of 225 patients who underwent EUS-guided FNA for pancreatic cysts between January 2014 and May 2015. For each patient, clinical findings, EUS features, cytopathology results, carcinoembryonic antigen analysis, and molecular testing of pancreatic cyst fluid were reviewed. Molecular testing included the assessment of hotspot mutations and deletions for KRAS, GNAS, VHL, TP53, PIK3CA, and PTEN.

Results

Diagnostic pathology results were available for 41 patients (18%), with 13 (6%) harboring advanced neoplasia. Among these cases, the AGA guidelines identified advanced neoplasia with 62% sensitivity, 79% specificity, 57% positive predictive value, and 82% negative predictive value. Moreover, the AGA guidelines missed 45% of intraductal papillary mucinous neoplasms with adenocarcinoma or high-grade dysplasia. For cases without confirmatory pathology, 27 of 184 patients (15%) with serous cystadenomas (SCAs) based on EUS findings and/or VHL alterations would continue magnetic resonance imaging (MRI) surveillance. In comparison, a novel algorithmic pathway using molecular testing of pancreatic cyst fluid detected advanced neoplasias with 100% sensitivity, 90% specificity, 79% positive predictive value, and 100% negative predictive value.

Conclusions

The AGA guidelines were inaccurate in detecting pancreatic cysts with advanced neoplasia. Furthermore, because the AGA guidelines manage all neoplastic cysts similarly, patients with SCAs will continue to undergo unnecessary MRI surveillance. The results of an alternative approach with integrative molecular testing are encouraging but require further validation.