Islet cell carcinoma: neuroendocrine tumors of the pancreas and periampullary region

Hematol Oncol Clin North Am. 2007 Jun;21(3):457-73; viii. doi: 10.1016/j.hoc.2007.04.005.

Abstract

Most patients who have islet cell tumors, except those who have insulinomas, present with locally advanced or metastatic disease. In contrast with patients who have adenocarcinoma of the pancreas, those who have islet cell carcinomas can achieve long-term survival even if their disease is advanced. Liver-directed therapies, somatostatin analogs, and interferon are not curative but can be used to relieve tumor-associated symptoms. Similarly, palliative chemotherapy has been used with limited success. Advances in our understanding of the molecular mechanisms underlying tumor progression have translated into intense interest in biologically based strategies to treat this disease.

Publication types

  • Review

MeSH terms

  • Carcinoma, Islet Cell* / diagnosis
  • Carcinoma, Islet Cell* / genetics
  • Carcinoma, Islet Cell* / therapy
  • Common Bile Duct Neoplasms* / diagnosis
  • Common Bile Duct Neoplasms* / genetics
  • Common Bile Duct Neoplasms* / therapy
  • Humans
  • Neuroendocrine Tumors* / diagnosis
  • Neuroendocrine Tumors* / genetics
  • Neuroendocrine Tumors* / therapy
  • Pancreatic Neoplasms* / diagnosis
  • Pancreatic Neoplasms* / genetics
  • Pancreatic Neoplasms* / therapy
  • Risk Factors