[Treatment of neuroendocrine tumours of the gastrointestinal tract]

Ugeskr Laeger. 2010 Oct 25;172(43):2942-5.
[Article in Danish]

Abstract

The prognosis of neuroendocrine tumours of the gastrointestinal tract and pancreas is difficult to estimate due to their heterogeneous nature. Survival without dissemination may reach 90%, while metastases reduce the 5-year survival to less than 50%. Radical surgery offers the only possibility of cure. Palliative therapy includes surgery and intra-arterial embolization of hepatic metastases, chemotherapy, biotherapy with interferon-alpha and radionuclear treatment. Tumour-targeted therapy with tyrosine kinase inhibitors, mammalian target of rapamycin inhibitors or monoclonal antibodies are under investigation in phase-III studies.

Publication types

  • English Abstract

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • Combined Modality Therapy
  • Gastrointestinal Neoplasms / drug therapy
  • Gastrointestinal Neoplasms / surgery
  • Gastrointestinal Neoplasms / therapy*
  • Humans
  • Liver Neoplasms / secondary
  • Liver Neoplasms / surgery
  • Neuroendocrine Tumors / drug therapy
  • Neuroendocrine Tumors / surgery
  • Neuroendocrine Tumors / therapy*
  • Palliative Care
  • Pancreatic Neoplasms / drug therapy
  • Pancreatic Neoplasms / surgery
  • Pancreatic Neoplasms / therapy*
  • Practice Guidelines as Topic
  • Prognosis

Substances

  • Antineoplastic Agents