[Treatment of systemic mastocytosis]

Rev Med Interne. 2003 Sep;24(9):594-601. doi: 10.1016/s0248-8663(03)00141-3.
[Article in French]

Abstract

Background: Systemic mastocytosis is a rare disease, characterized by mast cells proliferation in various organs. Two types of clinical manifestations can be distinguished: those related to mast cells mediators release and those related to tumoral proliferation involving different organs, these later defining aggressive systemic mastocytosis. Until recently, treatment was mainly symptomatic, without anti tumoral effect.

Recent facts: These last years, advances have been made in the understanding of the disease with the discovery of the c-kit oncogene mutation and the approach of the disease as a myeloproliferative disorder.

Perspectives: Based on experiences acquired in the treatment of this kind of disorders, evaluation of new therapeutics, such as cladribine or combination of interferon-alpha and cytarabine is in progress. At least, tyrosine kinase inhibitors, a new family of molecules, are able of inhibiting some types of the mutated c-kit protein and one of them, imatinib mesylate, has shown a great efficacy in the treatment of gastro intestinal stromal tumors (GIST) which also involves the c-kit mutation. By analogy, treatment of patients with c-kit susceptible mutation might be treated with this molecule.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Adrenal Cortex Hormones / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Benzamides
  • Cladribine / pharmacology*
  • Cytarabine / pharmacology*
  • Diphosphonates / pharmacology
  • Enzyme Inhibitors / pharmacology*
  • Histamine H1 Antagonists / pharmacology
  • Humans
  • Imatinib Mesylate
  • Interferon-alpha / pharmacology*
  • Mastocytosis, Systemic / drug therapy*
  • Mastocytosis, Systemic / physiopathology
  • Mastocytosis, Systemic / radiotherapy
  • Photochemotherapy
  • Piperazines / pharmacology*
  • Proto-Oncogene Proteins c-kit / pharmacology*
  • Pyrimidines / pharmacology*

Substances

  • Adrenal Cortex Hormones
  • Antineoplastic Agents
  • Benzamides
  • Diphosphonates
  • Enzyme Inhibitors
  • Histamine H1 Antagonists
  • Interferon-alpha
  • Piperazines
  • Pyrimidines
  • Cytarabine
  • Cladribine
  • Imatinib Mesylate
  • Proto-Oncogene Proteins c-kit