Molecular targeted therapy for neuroendocrine tumors

Hematol Oncol Clin North Am. 2007 Jun;21(3):575-81; x. doi: 10.1016/j.hoc.2007.04.001.

Abstract

Although endocrine tumors are often slow growing, most can be life threatening and are considered resistant to conventional cytotoxic chemotherapy. The recent emergence of molecularly targeted therapy in oncology has brought renewed interest in the development of novel agents for this rare group of diseases. Preliminary results from phase II studies have shown promising results for VEGF and mTOR inhibitors in carcinoid and islet cell carcinoma and RET inhibitors in medullary thyroid carcinoma. Large confirmatory studies are planned.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Humans
  • Lymphokines / antagonists & inhibitors
  • Neuroendocrine Tumors / drug therapy*
  • Platelet-Derived Growth Factor / antagonists & inhibitors
  • Protein Kinase Inhibitors / pharmacology
  • Protein Kinase Inhibitors / therapeutic use*
  • Protein Kinases / drug effects
  • Proto-Oncogene Proteins c-ret / antagonists & inhibitors
  • Receptors, Vascular Endothelial Growth Factor / antagonists & inhibitors
  • Structure-Activity Relationship
  • TOR Serine-Threonine Kinases

Substances

  • Antineoplastic Agents
  • Lymphokines
  • PDGFD protein, human
  • Platelet-Derived Growth Factor
  • Protein Kinase Inhibitors
  • Protein Kinases
  • MTOR protein, human
  • Proto-Oncogene Proteins c-ret
  • Receptors, Vascular Endothelial Growth Factor
  • TOR Serine-Threonine Kinases