Mutations with epigenetic effects in myeloproliferative neoplasms and recent progress in treatment: Proceedings from the 5th International Post-ASH Symposium

A. Tefferi, O. Abdel-Wahab, F. C. Ervantes, J. D. Crispino, G. Finazzi, F. Girodon, H. Gisslinger, J. Gotlib, J. J. Kiladjian, R. L. Levine, J. D. Licht, A. Mullally, O. Odenike, A. Pardanani, R. T. Silver, E. Solary, T. Mughal

Research output: Contribution to journalArticlepeer-review

8 Scopus citations

Abstract

Immediately following the 2010 annual American Society of Hematology (ASH) meeting, the 5th International Post-ASH Symposium on Chronic Myelogenous Leukemia and BCRABL1-Negative Myeloproliferative Neoplasms (MPNs) took place on 7-8 December 2010 in Orlando, Florida, USA. During this meeting, the most recent advances in laboratory research and clinical practice, including those that were presented at the 2010 ASH meeting, were discussed among recognized authorities in the field. The current paper summarizes the proceedings of this meeting in BCR-ABL1-negative MPN. We provide a detailed overview of new mutations with putative epigenetic effects (TET oncogene family member 2 (TET2), additional sex comb-like 1 (ASXL1), isocitrate dehydrogenase (IDH) and enhancer of zeste homolog 2 (EZH2)) and an update on treatment with Janus kinase (JAK) inhibitors, pomalidomide, everolimus, interferon-a, midostaurin and cladribine. In addition, the new 'Dynamic International Prognostic Scoring System (DIPSS)-plus' prognostic model for primary myelofibrosis (PMF) and the clinical relevance of distinguishing essential thrombocythemia from prefibrotic PMF are discussed.

Original languageEnglish (US)
Article numbere7
JournalBlood cancer journal
Volume1
Issue number3
DOIs
StatePublished - Mar 2011

Keywords

  • Mastocytosis
  • Myelofibrosis
  • Myeloproliferative
  • Polycythemia
  • Thrombocythemia

ASJC Scopus subject areas

  • Hematology
  • Oncology

Fingerprint

Dive into the research topics of 'Mutations with epigenetic effects in myeloproliferative neoplasms and recent progress in treatment: Proceedings from the 5th International Post-ASH Symposium'. Together they form a unique fingerprint.

Cite this