A Survival Analysis of Patients with Localized, Asymptomatic Pancreatic Neuroendocrine Tumors: No Surgical Survival Benefit when Examining Appropriately Selected Outcomes
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology,Surgery
Link
http://link.springer.com/content/pdf/10.1007/s11605-019-04433-4.pdf
Reference22 articles.
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2. Dasari A, Shen C, Halperin D, Zhao B, Zhou S, Xu Y et al. Trends in the Incidence, Prevalence, and Survival Outcomes in Patients With Neuroendocrine Tumors in the United States. JAMA Oncol 2017;3(10):1335–42. doi:https://doi.org/10.1001/jamaoncol.2017.0589.
3. Zerbi A, Falconi M, Rindi G, Delle Fave G, Tomassetti P, Pasquali C et al. Clinicopathological features of pancreatic endocrine tumors: a prospective multicenter study in Italy of 297 sporadic cases. Am J Gastroenterol 2010;105(6):1421–9. doi:https://doi.org/10.1038/ajg.2009.747.
4. Mansour JC, Chavin K, Morris-Stiff G, Warner SG, Cardona K, Fong ZV et al. Management of asymptomatic, well-differentiated PNETs: results of the Delphi consensus process of the Americas Hepato-Pancreato-Biliary Association. HPB : the official journal of the International Hepato Pancreato Biliary Association 2018. https://doi.org/10.1016/j.hpb.2018.09.020.
5. Kulke MH, Anthony LB, Bushnell DL, de Herder WW, Goldsmith SJ, Klimstra DS et al. NANETS treatment guidelines: well-differentiated neuroendocrine tumors of the stomach and pancreas. Pancreas. 2010;39(6):735–52. doi:https://doi.org/10.1097/MPA.0b013e3181ebb168.
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