Minimizing risk of hypomethylating agent failure in patients with higher-risk MDS and practical management recommendations

Leuk Res. 2014 Dec;38(12):1381-91. doi: 10.1016/j.leukres.2014.09.008. Epub 2014 Sep 22.

Abstract

In Europe, azacitidine is the only hypomethylating agent approved for the treatment of patients with int-2-/high-risk myelodysplastic syndromes, offering significantly improved survival compared with conventional care. However, not all patients treated with azacitidine respond to treatment, and the vast majority of responders subsequently relapse. Currently, no standard care regimens have been established for patients after failure of azacitidine. Here, we discuss treatment options after loss of response or progression on azacitidine. In addition, we briefly consider optimization of first-line treatment along with potential biomarkers for identifying and monitoring response during treatment with azacitidine.

Keywords: Azacitidine; Consensus; Hypomethylating agents; MDS; Refractory; Relapse; Salvage therapy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antimetabolites, Antineoplastic / therapeutic use*
  • Azacitidine / therapeutic use*
  • Biomarkers
  • Disease-Free Survival
  • Europe / epidemiology
  • Humans
  • Myelodysplastic Syndromes / drug therapy*
  • Myelodysplastic Syndromes / mortality
  • Practice Guidelines as Topic
  • Risk Factors
  • Survival Rate

Substances

  • Antimetabolites, Antineoplastic
  • Biomarkers
  • Azacitidine