Background & aims: Pancreatic cysts often pose challenges in predicting malignant progression. Next-generation sequencing has become an appealing ancillary diagnostic test. The diagnostic performance is well characterized, but the impact on clinical management remains unclear. We aim to evaluate the efficacy of integrating NGS into cyst management algorithms.
Methods: This single-center retrospective study included 441 adult patients who were seen at our high-risk pancreatic lesion clinic between 2016 and 2022 and had NGS data available. Performance characteristics of PancreaSeq were calculated. The clinical utility of PancreaSeq in guiding surgical management and differentiating cyst type was evaluated.
Results: High-risk mutations (n=25) demonstrated 72.7% (95% CI: 49.8% - 89.3%) sensitivity, 97.8% (95% CI: 96% - 99%) specificity, and area under receiver operating curve 0.85 (95% CI: 0.76 - 0.95) in predicting advanced neoplasia. NGS detected KRAS or GNAS mutations in 179/324 (55.3%) and VHL mutations in 15/324 (3.4%) with unclear cyst type, facilitating decision regarding surveillance versus clinic discharge. Among 27 patients with isolated pancreatic duct dilation, 12 (48.1%) had mutations consistent with mucinous neoplasms leading to a diagnosis of main duct intraductal papillary mucinous neoplasm. These findings resulted in surgical management for six patients. Overall, 115 of 441 (26.1%) patients had some management change after undergoing NGS.
Conclusion: NGS informed surgical decision-making, cyst type differentiation, and evaluation of pancreatic duct dilation, leading to changes in management. Indeed, NGS emerges as a useful tool in select patients with pancreatic lesions by improving diagnostic precision and guiding patient care paths.
Keywords: PancreaSeq; Pancreatic cyst; intraductal papillary mucinous neoplasm; next-generation sequencing; pancreatic cancer.
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