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Pancreatic neuroendocrine tumors: Surgical outcomes and survival analysis
Pancreatic neuroendocrine tumors are rare, with rising incidence and limited clinicopathological studies. Adult patients with pNET at a single tertiary care center were retrospectively evaluated. In total, 87 patients with histologically confirmed pNET who underwent resection were evaluated. 11% of...
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Published in: | The American journal of surgery 2021-03, Vol.221 (3), p.529-533 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Pancreatic neuroendocrine tumors are rare, with rising incidence and limited clinicopathological studies.
Adult patients with pNET at a single tertiary care center were retrospectively evaluated.
In total, 87 patients with histologically confirmed pNET who underwent resection were evaluated. 11% of patients had functioning pNETs: 9 insulinoma and 1 VIPoma. The majority (88.5%) were nonfunctioning. The most common surgical procedure performed was distal pancreatectomy with splenectomy (36.8%). 35.6% of cases were performed with minimally invasive surgery (MIS). MIS patients had fewer postoperative complications, shorter length of stay, and fewer ICU admissions.Disease-free survival (DFS) was unaffected by tumor size (p = 0.5) or lymph node status (p = 0.62). Patients with high-grade (G3) tumors experienced significantly shorter DFS (p = 0.02).
This series demonstrates that survival in patients with pNET is driven mostly by tumor grade, though overall most have long-term survival after surgical resection. Additionally, an MIS approach is efficacious in appropriately selected cases.
Survival for pancreatic neuroendocrine tumors is driven mostly by tumor grade. Minimally invasive surgery is a safe and effective approach to resecting these tumors. |
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ISSN: | 0002-9610 1879-1883 |
DOI: | 10.1016/j.amjsurg.2020.12.037 |