| Literature DB >> 28254862 |
Peter Valent1, Cem Akin2, Karin Hartmann3, Gunnar Nilsson4, Andreas Reiter5, Olivier Hermine6, Karl Sotlar7, Wolfgang R Sperr8, Luis Escribano9, Tracy I George10, Hanneke C Kluin-Nelemans11, Celalettin Ustun12, Massimo Triggiani13, Knut Brockow14, Jason Gotlib15, Alberto Orfao9, Lawrence B Schwartz16, Sigurd Broesby-Olsen17, Carsten Bindslev-Jensen17, Petri T Kovanen18, Stephen J Galli19, K Frank Austen2, Daniel A Arber19, Hans-Peter Horny20, Michel Arock21, Dean D Metcalfe22.
Abstract
Mastocytosis is a term used to denote a heterogeneous group of conditions defined by the expansion and accumulation of clonal (neoplastic) tissue mast cells in various organs. The classification of the World Health Organization (WHO) divides the disease into cutaneous mastocytosis, systemic mastocytosis, and localized mast cell tumors. On the basis of histomorphologic criteria, clinical parameters, and organ involvement, systemic mastocytosis is further divided into indolent systemic mastocytosis and advanced systemic mastocytosis variants, including aggressive systemic mastocytosis and mast cell leukemia. The clinical impact and prognostic value of this classification has been confirmed in numerous studies, and its basic concept remains valid. However, refinements have recently been proposed by the consensus group, the WHO, and the European Competence Network on Mastocytosis. In addition, new treatment options are available for patients with advanced systemic mastocytosis, including allogeneic hematopoietic stem cell transplantation and multikinase inhibitors directed against KIT D816V and other key signaling molecules. Our current article provides an overview of recent advances in the field of mastocytosis, with emphasis on classification, prognostication, and emerging new treatment options in advanced systemic mastocytosis. Cancer Res; 77(6); 1261-70. ©2017 AACR. ©2017 American Association for Cancer Research.Entities:
Mesh:
Year: 2017 PMID: 28254862 PMCID: PMC5354959 DOI: 10.1158/0008-5472.CAN-16-2234
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701