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Advances in Understanding and Management of Myeloproliferative Neoplasms

Journal

CA-A CANCER JOURNAL FOR CLINICIANS
Volume 59, Issue 3, Pages 171-191

Publisher

WILEY
DOI: 10.3322/caac.20009

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Funding

  1. Associazione Italiana per la Ricerca sul Cancro, Milano
  2. Istituto Toscano Tumori
  3. MIUR [2006067001_003]

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According to the 2008 World Health Organization, classification system for hematologic malignancies, the myeloproliferative neoplasms (MPN) include chronic myelogenous leukemia, polycythemia vera, essential thrombocythemia, primary myelofibrosis, mastocytosis, chronic eosinophilic leukemia-not otherwise specified, chronic neutrophilic leukemia, and MPN, unclassifiable. All of these clinicopathologic entities are characterized by stem cell-derived clonal myeloproliferation, and their phenotypic diversity is ascribed to the occurrence of distinct oncogenic events. In the last 4 years, new JAK2 and MPL mutations have been added to previously described ABL and KIT mutations as molecular markers of disease in MPN. These discoveries have markedly simplified the approach to clinical diagnosis and have also provided molecular targets for the development of small-molecule drugs. In the current article, the authors provide a clinically oriented overview of MPNs in terms of their molecular pathogenesis, classification, diagnosis, and management. CA Cancer J Clin 2009;59:171-191. (C) 2009 American Cancer Society, Inc.

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