Current status and future directions of molecularly targeted therapies and immunotherapies for melanoma

Semin Cutan Med Surg. 2014 Jun;33(2):60-7. doi: 10.12788/j.sder.0081.

Abstract

Key molecular and immunological insights over the past decade have radically changed the face of therapy in melanoma. Whereas 5 years ago, treatment for advanced melanoma was restricted to the alkylating agent dacarbazine and the immunostimulants interleukin-2 and interferon-α-2b, today the therapeutic menu includes precise therapies that target key determinants in oncogenic pathways and immune checkpoints. In this chapter, we will review the current status and future directions of targeted therapies for melanoma directed at mitogen-activated pathways and immune checkpoints.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / therapeutic use
  • CTLA-4 Antigen / antagonists & inhibitors
  • Humans
  • Immunologic Factors / therapeutic use
  • Immunotherapy*
  • Interferon-alpha / therapeutic use
  • Interleukin-2 / therapeutic use
  • Melanoma / genetics
  • Melanoma / immunology
  • Melanoma / therapy*
  • Mitogen-Activated Protein Kinase Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinase Kinases / genetics
  • Molecular Targeted Therapy*
  • Mutation
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Protein Kinase Inhibitors / therapeutic use
  • Proto-Oncogene Proteins B-raf / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins c-kit / genetics
  • Skin Neoplasms / genetics
  • Skin Neoplasms / immunology
  • Skin Neoplasms / therapy*

Substances

  • Antineoplastic Agents
  • CTLA-4 Antigen
  • Immunologic Factors
  • Interferon-alpha
  • Interleukin-2
  • Programmed Cell Death 1 Receptor
  • Protein Kinase Inhibitors
  • Proto-Oncogene Proteins c-kit
  • Proto-Oncogene Proteins B-raf
  • Mitogen-Activated Protein Kinase Kinases