Role of chromogranin A-derived fragments after resection of nonfunctioning pancreatic neuroendocrine tumors
Author:
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Link
https://link.springer.com/content/pdf/10.1007/s40618-022-01750-5.pdf
Reference40 articles.
1. Dasari A, Shen C, Halperin D et al (2017) Trends in the incidence, prevalence, and survival outcomes in patients with neuroendocrine tumors in the United States. JAMA Oncol 3:1335–1342. https://doi.org/10.1001/jamaoncol.2017.0589
2. Vagefi PA, Razo O, Deshpande V et al (2007) Evolving patterns in the detection and outcomes of pancreatic neuroendocrine neoplasms: the Massachusetts General Hospital experience from 1977 to 2005. Arch Surg 142:347–354. https://doi.org/10.1001/archsurg.142.4.347
3. Falconi M, Eriksson B, Kaltsas G et al (2016) ENETS consensus guidelines update for the management of patients with functional pancreatic neuroendocrine tumors and non-functional pancreatic neuroendocrine tumors. Neuroendocrinology 103:153–371. https://doi.org/10.1159/000443171
4. Genç CG, Falconi M, Partelli S et al (2018) Recurrence of pancreatic neuroendocrine tumors and survival predicted by Ki67. Ann Surg Oncol 25:2467–2474. https://doi.org/10.1245/s10434-018-6518-2
5. Hashim YM, Trinkaus KM, Linehan DC et al (2014) Regional lymphadenectomy is indicated in the surgical treatment of pancreatic neuroendocrine tumors (PNETs). Ann Surg 259:197–203. https://doi.org/10.1097/SLA.0000000000000348
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1. Recent developments in the diagnosis of pancreatic neuroendocrine neoplasms;Expert Review of Gastroenterology & Hepatology;2024-05-02
2. The immunomodulatory functions of chromogranin A-derived peptide pancreastatin;Peptides;2022-12
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