New strategies in ewing sarcoma: lost in translation?

Clin Cancer Res. 2014 Jun 15;20(12):3050-6. doi: 10.1158/1078-0432.CCR-13-0633. Epub 2014 Apr 22.

Abstract

Ewing sarcoma is the second most common pediatric malignant bone tumor. Aggressive multimodality therapy has led to an improvement in outcomes, particularly in patients with localized disease. However, therapy-related toxicities are not trivial, and the prognosis for patients with relapsed and/or metastatic disease continues to be poor. In this article, we outline some of the promising therapies that have the potential to change the Ewing sarcoma therapeutic paradigm in the not-too-distant future: insulin-like growth factor receptor inhibitors, targeting of the fusion protein, epigenetic manipulation, PARP inhibitors, and immunotherapy.

MeSH terms

  • Antineoplastic Agents / therapeutic use*
  • Bone Neoplasms / immunology
  • Bone Neoplasms / metabolism
  • Bone Neoplasms / therapy*
  • Enzyme Inhibitors / therapeutic use*
  • Humans
  • Immunotherapy*
  • Molecular Targeted Therapy*
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Receptors, Somatomedin / antagonists & inhibitors
  • Sarcoma, Ewing / immunology
  • Sarcoma, Ewing / metabolism
  • Sarcoma, Ewing / therapy*

Substances

  • Antineoplastic Agents
  • Enzyme Inhibitors
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Receptors, Somatomedin
  • PARP1 protein, human
  • Poly (ADP-Ribose) Polymerase-1