Emerging translational science discoveries, clonal approaches, and treatment trends in chronic myeloproliferative neoplasms

Hematol Oncol. 2019 Aug;37(3):240-252. doi: 10.1002/hon.2622. Epub 2019 Jun 20.

Abstract

The 60th American Society of Hematology (ASH) held in San Diego in December 2018 was followed by the 13th Post-ASH chronic myeloproliferative neoplasms (MPNs) workshop on December 4 and 5, 2018. This closed annual workshop, first introduced in 2006 by Goldman and Mughal, was organized in collaboration with Alpine Oncology Foundation and allowed experts in preclinical and clinical research in the chronic MPNs to discuss the current scenario, including relevant presentations at ASH, and address pivotal open questions that impact translational research and clinical management. This review is based on the presentations and deliberations at this workshop, and rather than provide a resume of the proceedings, we have selected some of the important translational science and treatment issues that require clarity. We discuss the experimental and observational evidence to support the intimate interaction between aging, inflammation, and clonal evolution of MPNs, the clinical impact of the unfolding mutational landscape on the emerging targets and treatment of MPNs, new methods to detect clonal heterogeneity, the challenges in managing childhood and adolescent MPN, and reflect on the treatment of systemic mastocytosis (SM) following the licensing of midostaurin.

Keywords: IFNα; MPNs; clonal heterogeneity; inflammaging; investigational therapies.

Publication types

  • Review

MeSH terms

  • Aging
  • Animals
  • Congresses as Topic
  • DNA Mutational Analysis
  • Humans
  • Inflammation
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive / therapy
  • Mastocytosis / therapy
  • Medical Oncology / methods
  • Medical Oncology / trends
  • Mice
  • Mutation
  • Myeloproliferative Disorders / therapy*
  • Prognosis
  • Societies, Medical
  • Staurosporine / analogs & derivatives
  • Staurosporine / therapeutic use
  • Translational Research, Biomedical / methods*
  • Translational Research, Biomedical / trends*
  • United States

Substances

  • Staurosporine
  • midostaurin