New therapeutic approaches in myelodysplastic syndromes: Hypomethylating agents and lenalidomide

Exp Hematol. 2015 Aug;43(8):661-72. doi: 10.1016/j.exphem.2015.05.014. Epub 2015 Jun 27.

Abstract

Recent advances in the treatment of myelodysplastic syndromes have come from the use of the hypomethylating agents decitabine and azacitidine as well as the immunomodulatory drug lenalidomide. Their clinical benefit has been demonstrated by randomized phase III clinical trials, mostly in high-risk and del(5q) myelodysplastic syndromes, respectively. Neither drug, however, appears to eradicate myelodysplastic stem cells, and thus they currently do not represent curative options. Here, we review data from both clinical and translational research on those drugs to identify their molecular and cellular mechanisms of action and to delineate paths for improved treatment allocation and further therapeutic advances in myelodysplastic syndromes.

Publication types

  • Review

MeSH terms

  • Angiogenesis Inhibitors / therapeutic use*
  • Animals
  • Antimetabolites, Antineoplastic / therapeutic use*
  • Azacitidine / analogs & derivatives*
  • Azacitidine / therapeutic use*
  • Clinical Trials, Phase III as Topic
  • Decitabine
  • Humans
  • Lenalidomide
  • Myelodysplastic Syndromes / drug therapy*
  • Myelodysplastic Syndromes / pathology
  • Randomized Controlled Trials as Topic
  • Thalidomide / analogs & derivatives*
  • Thalidomide / therapeutic use
  • Translational Research, Biomedical

Substances

  • Angiogenesis Inhibitors
  • Antimetabolites, Antineoplastic
  • Thalidomide
  • Decitabine
  • Lenalidomide
  • Azacitidine