Pathologic Grade and Tumor Size are Associated with Recurrence-Free Survival in Patients with Duodenal Neuroendocrine Tumors |
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Authors: | Brian R. Untch Keisha P. Bonner Kevin K. Roggin Diane Reidy-Lagunes David S. Klimstra Mark A. Schattner Yuman Fong Peter J. Allen Michael I. D’Angelica Ronald P. DeMatteo William R. Jarnagin T. Peter Kingham Laura H. Tang |
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Affiliation: | 1. Department of Surgery, Memorial Sloan-Kettering Cancer Center, 1275 York Ave, New York, NY, 10065, USA 2. Department of Surgery, University of Chicago, Chicago, IL, USA 3. Department of Medicine, Gastrointestinal Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA 4. Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY, USA 5. Department of Medicine, Gastroenterology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA
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Abstract: |
Background Duodenal neuroendocrine tumors are rare and few studies exist to guide surgical management. This study identifies factors associated with recurrence after resection. Methods A retrospective, single institution review was performed between 1983 and 2011 on patients with a pathologic diagnosis of duodenal neuroendocrine tumor. Tumor grade was assigned based on WHO 2010 criteria (Ki-67 and mitotic rate). Results Seventy-five patients were identified that underwent curative resection. This included 12 patients with endoscopic mucosal resection, 34 that had local resection, and 29 that underwent pancreaticoduodenectomy. Two-year and 5-year recurrence-free survival was 84 and 81 %, respectively. There were 11 tumor recurrences (either local or distant), and four patients died of their disease (3/4 had high-grade lesions) with an overall median follow-up of 27 months. On univariate analysis, tumor size and tumor grade were identified as being associated with recurrence, but not intervention type, lymph node metastases, ampullary location, or margin status. Conclusions Tumor grade and size are associated with recurrence-free survival in duodenal neuroendocrine tumors. When feasible, a less aggressive surgical approach to treat low-grade and low-stage duodenal NETs should be considered. |
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