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Medical Management of Pancreatic Cysts
Jeffrey H. Lee, MD, MPH, FACG, FASGE, AGAF Professor and Director, Advanced Endoscopy Fellowship and Training MD Anderson Cancer Center
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Pancreatic Cystic Lesions (PCLs)
Non-neoplastic pancreatic cysts Pseudocyst Congenital cyst Retention cyst Neoplastic pancreatic cysts (pancreatic cystic neoplasms) Mucinous cystic lesions Intraductal papillary mucinous neoplasm (IPMN) Mucinous cystic neoplasm (MCN) Non-mucinous cystic lesions Serous cystic neoplasm (SCN) Solid-pseudopapillary neoplasm (SPN) Cystic neuroendocrine neoplasm Acinar-cell cystic neoplasm Ductal adenocarcinoma with cystic degeneration
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Pancreatic Cystic Neoplasms (PCNs)
Prevalence Imaging-based studies: 1.2% - 1.9% In autopsy series of 300 patients 186 cystic lesions in 73 of 300 patients (24.3%) Increases with age Yoon et al. Clin North Am 1012 Laffan et al. Am J Roentgenol 2008
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WHO Classification of PCNs
Benign Serous Cystadenoma (SCN) Premalignant IPMN with low- or intermediate-grade dysplasia IPMN with high grade dysplasia Mucinous cystic neoplasm (MCN) with low- or intermediate-grade dysplasia Mucinous cystic neoplasm (MCN) with high-grade dysplasia Malignant Mucinous cystadenocarcinoma IPMN with an associated invasive carcinoma MCN with an associated invasive carcinoma Solid-pseudopapillary neoplasm
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Pancreatic Cysts Tanaka et al. Pancreatology 2012 (International Consensus Guidelines)
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Solid Pseudopapillary Neoplasms
9 (15%) malignant No factors that predicted malignancy N = 106 who underwent surgery 17 high-grade dysplasia >5 cm was associated with an increased risk of high-grade dysplasia Lee et al. Arch Surg 2008 Kim et al. Br J Surg 2014
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Pancreatic Cystic Lesions
“To be, or not to be, that is the question…” - William Shakespeare’s play Hamlet “To operate or to observe, that is the question.” -Gastroenterologists and surgeons managing pancreatic cysts
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Are these results acceptable?
N=74 Preoperative classification as mucinous or nonmucinous was correct in 74% Path with higher malignancy potential than the preop diagnosis in 7% Benign path with preop diagnosis of premalignant or malignant in 20% Cho et al. Ann Surg Oncol 2009
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Goals in Managing PCNs Desirable outcomes Undesirable outcomes
Benign PCN - observation Malignant PCN - resection Premalignant PCN - resection before malignant transformation occurs Undesirable outcomes Benign PCN undergoing resection Malignant PCN being observed Premalignant PCN - resection after malignant transformation occurs
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Pancreatic Cystic Lesions
Cysts to Resect Cysts to Observe Cystadenocarcinoma Malignant IPMN Main duct IPMN Branch duct-IPMN (BD-IPMN) with high risk features Solid pseudopapillary neoplasm Cystic neuroendocrine tumor >2 cm Pseudocyst Serous cystadenoma (SCN) BD-IPMN without worrisome features or high risk features Small cystic neuroendocrine tumor
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Pancreatic Cystic Lesions
Easy to diagnose w/o EUS FNA Difficult to diagnose w/o EUS FNA Pseudocyst with history of pancreatitis Typical serous cystadenoma Typical mucinous cystadenoma Typical IPMN Cystadenocarcinoma Solid pseudopapillary neoplasm Macrocystic SCN vs. MCN Macro and Microcystic SCN vs. BD – IPMN Pseudocyst without history of pancreatitis vs. MCN Cystic neuroendocrine tumor Mural nodule/mucus plug in PD or PD side branch
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Diagnostic Tools and Their Limitations
CT and MRI CLPs have heterogeneous appearance on imaging and share many morphological features EUS Technical expertise may not be available Accuracy no greater than 80% EUS FNA Usually paucity of cells Nondiagnostic Cytobrushing significantly more likely to detect intracellular mucin than FNA (62% vs. 23%) Cystic fluid Cytology Amylase Viscosity CEA Needle based confocal laser endomicroscopy (nCLE)
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Serous Cystadenoma CT, PV phase 3D T1 FS post Gad 2D T1 Out-of-Phase
Consider showing case of metastatic serous cystadenoma T2 fat sat Diffusion ADC Map Eric Tamm
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Mucinous Cystadenoma T1 Delayed Post Gadolinium, Fat Sat T2, Fat Sat
Capsule T2 hypointense Eric Tamm 14
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Mucinous Cystadenocarcinoma
T1 Delayed Post Gadolinium, Fat Sat, enh capsule T2, Fat Sat, Capsule T2 hypointense Eric Tamm
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Mixed Main Duct and Side Branch IPMN
3D MIP MRCP 3D MRCP Single Image Eric Tamm
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Pseudopapillary Tumor
Eric Tamm
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Cystic Islet Cell tumor
Eric Tamm
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Cooperative Pancreatic Cyst Study
112 surgical resection; 68 mucinous, 7 serous, 27 inflammatory, 5 endocrine, and 5 others Brugge et al. Gastroenterol 2004
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Cooperative Pancreatic Cyst Study
Brugge et al. Gastroenterol 2004
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Cooperative Pancreatic Cyst Study
Brugge et al. Gastroenterol 2004
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nCLE Konda et al. Endoscopy 2013 Nakai et al. Gastrointest Endosc 2015
Napoleon et al. Endoscopy 2014
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Diagnostic Tools and Their Limitations
CT and MRI CLPs have heterogeneous appearance on imaging and share many morphological features EUS Technical expertise may not be available Accuracy no greater than 80% EUS FNA Usually paucity of cells Nondiagnostic Cytobrushing significantly more likely to detect intracellular mucin than FNA (62% vs. 23%) Cystic fluid Cytology Amylase Viscosity CEA nCLE Therefore, guidelines would be extremely useful in the initial management of CLPs if they can be applied to CLPs detected on cross-sectional imaging
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Guidelines ASGE guidelines 2005
International Consensus Guidelines 2006 (Sendai) ACG guidelines 2007 International Consensus Guidelines 2012 (Fukuoka) AGA guidelines 2015
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Tanaka et al. Pancreatology 2006 (Sendai Guidelines)
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Tanaka et al. Pancreatology 2012
Lennon and Wolfgang. J Gastrointest Surg 2013
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Vege et al. Gastroenterol 2015 (AGA)
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Lennon and Wolfgang. J Gastrointest Surg 2013
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Sendai Consensus Guidelines
Risk stratification for IPMN and MCN Resect all main PD IPMN, mixed-type IPMN and MCN Resect BD-IPMN with high risk features Intracystic mural nodule Main PD dilation > 10 mm >3 cm Observe BD-IPMN without high risk features Tanaka et al. Pancreatology 2006
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Fukuoka Consensus Guidelines
Risk stratification for IPMN and MCN Resect BD-IPMN with high risk features Main PD dilation > 10 mm Jaundice resulting from PCN in the head Enhancing solid nodule within the cyst Worrisome features not necessarily requiring immediate resection Main-duct IPMN with PD 5-9 mm Symptomatic pancreatitis >3 cm Thickened/enhancing cyst walls Nonenhancing mural nodule Abrupt change in caliber of the PD Tanaka et al. Pancreatology 2012
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A Population-Based Cohort Study on PCN
N = 1735 with PCN, retrospective Median follow-up 23.4 months Incidence of malignancy: 0.4 % / year with a standardized incidence ratio of 35 Increased risk for malignancy Larger size >3 cm, 9.3 % risk 1-3 cm with main PD dilation, 13.6 % risk Main PD dilation Absence sepatations with calcification Growth of the cyst during follow-up Wu et al. Am J Gastroenterol 2014
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How did we fare with Sendai Consensus Guidelines?
<3 cm; rate of malignancy 34% N=123 BD-IPMN 69 Sendai negative; 17 (25%) with HGD or invasive ductal carcinoma Limitations No details on worrisome features, changes in size Prescreening with EUS; selection bias Wong et al. J Gastrointest Surg 2013 Fritz et al. Ann Surg 2012
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How did we fare with Fukuoka Consensus Guidelines?
N=563, 240 resection <3 cm BD-IPMNs; 6.5 % with HGD >3cm; 8.8% with HGD including one invasive carcinoma Sahora et al. Ann Surg 2013
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Comparison of the Utility of Sendai and Fukuoka guidelines in Clinical Setting
N=317 surgical resection of PCLs (47 EUS) 56% were potentially malignant/malignant Fukuoka guidelines vs. Sendai guidelines for pre-malignant/malignant lesions PPV: 88 vs. 67 % NPV: 92.5 vs. 88 % Retrospective study IPMNs comprised only 21 % of all PCLs Goh et al. Ann Surg Oncol 2014
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EUS – guided Therapy Authors Year # of patients Agents used
# of patients in follow-up Follow-up # with resolution of cyst Remarks Gan et al. 2005 25 Ethanol 23 6 – 12 m 8 (35%) Non-significant trend, >50% Oh et al. 2008 14 + Paclitaxel 9 m (median) 11 (79%) 1 mild pancreatitis 2011 52 Ethanol lavage followed by Paclitaxel 47 21.7 m (median) 29 (62%) CR 6 (13%) PR 12 (36%) NR 1 mid pancreatitis & Splenic vein obliteration Gan et al. Gastrointest Endosc 2005 Oh et al. Gastrointest Endosc 2008 Oh et al Gastroenterology 2011
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Acknowledgements Eric Tamm, MD; Radiology Dan Davis, DO; Pathology
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