Pancreatic Cyst Clinical Trial
Official title:
Prospective Analysis About the Utility of Contrast Enhanced Endoscopic Ultrasound and Molecular Analysis in the Study of Pancreatic Cyst
This study evaluates the use of contrast-enhanced harmonic endoscopic ultrasound (CH-EUS) and cyst fluid molecular analysis in the differential diagnosis of pancreatic cysts and the detection of malignancy.
Pancreatic cyst are a frequent finding on cross-sectional imaging on general population. They
are identified in up to 3% of the abdominal computed tomographies (CT) and 20% of magnetic
resonance imaging (MRI) performed for other reasons but the risk of malignancy in pancreatic
cysts discovered incidentally is low, representing 1-5% of the total malignant pancreatic
neoplasms.
Pancreatic cysts are a broad group of pancreatic lesions that can be divided into benign and
premalignant or malignant lesions. Pseudocyst and serous cystic neoplasm (SCN) don´t have
malignant potential while others like mucinous cysts are premalignant lesions. But not all
mucinous neoplasms have the same risk of malignancy. According to recent publications
mucinous cystic neoplasm (MCN) have a potential for malignancy of around 15%, main duct
intrapapillary mucinous neoplasm (MD-IPMN) of 62% and branch duct IPMN (BD-IPMN) of 25%. The
correct identification of these premalignant lesions will allow to optimize the treatment and
follow-up of these patients, but in many cases it is difficult to accurately differentiate
between different types of cysts and their risk of malignancy. The differentiation between
lmucinous and non-mucinous cysts is suboptimal, with diagnostic accuracy for CT and MRI of
61% and 50-73% with endoscopic ultrasound (EUS). The endosonographic characteristics that
have been related with malignancy are the size larger than 3 cm, the presence of a solid
component, wall thickening, Wirsung dilation, abrupt change of the size of the main
pancreatic duct with distal atrophy of the gland and the presence of lymphadenopathies.
However, endosonographic characteristics are not sufficient as an individual predictor of
malignancy.
The puncture of the cyst and fine-needle aspiration (EUS-FNA) with biochemical and
cytological assessment is generally indicated to differentiate between cysts and to asses for
malignancy. The determination of carcinoembryonic antigen (CEA) and amylase have low
specificity for the detection of malignancy and for mucinous cyst, and the cytological
assessment is highly specific but lacks of sensibility (50%). So further methods are
requested for an adequate detection of premalignant and malignant cyst.
Contrast-enhanced harmonic endoscopic ultrasound uses an ultrasonographic contrast agent to
visualize blood flow in fine vessels and may aid in the diagnosis of pancreatic cysts by
enabling assessment of the vascularization of structures such as cyst walls, septa, or mural
nodules. Furthermore it allows the correct differentiation between contrast-enhanced mural
nodules, that predict for malignancy, from non-enhancing mucus clots.
The molecular analysis of cyst fluid may detect mutations that are associated with
premalignant cyst and with malignancy. Kirsten rat sarcoma (KRAS) gene has been related with
mucinous cyst while von Hippel-Lindau gene (VHL) is present in serous cyst.
This study evaluates the use of contrast-enhanced EUS and the molecular analysis for
pancreatic cyst diagnosis and malignant detection, and if their use may modify cyst
management.
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