Therapeutic strategies for the treatment of neuroblastoma

Curr Opin Investig Drugs. 2005 Dec;6(12):1200-14.

Abstract

Neuroblastoma, the most common extracranial solid tumor in children, has a highly heterogeneous clinical presentation and course. Current risk-based therapy is usually effective in patients who have intermediate risk features, however, intensive treatment of advanced neuroblastoma in children over two years of age is far from satisfactory. Current therapeutic approaches include the optimization of pharmacokinetic and pharmacodynamic properties of conventional agents, as well as the development of novel targeted drugs, such as signal transduction and angiogenesis inhibitors, apoptosis/differentiation stimulators and immunotherapeutics. This review provides an overview of current treatment options and future perspectives for the therapy and prevention of neuroblastoma.

Publication types

  • Review

MeSH terms

  • Administration, Oral
  • Angiogenesis Inhibitors / administration & dosage*
  • Angiogenesis Inhibitors / therapeutic use
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / therapeutic use
  • Apoptosis / drug effects
  • Cancer Vaccines / administration & dosage*
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Drug Combinations
  • Drug Delivery Systems*
  • Drug Design
  • Drug Resistance, Neoplasm
  • Drug Therapy, Combination
  • Humans
  • Immunotherapy
  • N-Myc Proto-Oncogene Protein
  • Neuroblastoma / drug therapy*
  • Neuroblastoma / genetics
  • Neuroblastoma / immunology
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Oncogene Proteins / genetics
  • Oncogene Proteins / metabolism
  • Randomized Controlled Trials as Topic
  • Signal Transduction / drug effects

Substances

  • Angiogenesis Inhibitors
  • Antineoplastic Agents
  • Cancer Vaccines
  • Drug Combinations
  • MYCN protein, human
  • N-Myc Proto-Oncogene Protein
  • Nuclear Proteins
  • Oncogene Proteins