Advances in the Classification and Treatment of Mastocytosis: Current Status and Outlook toward the Future

Peter Valent(Ludwig Boltzmann Institute for Cardiovascular Research), Cem Akin(Brigham and Women's Hospital), Karin Hartmann(Institute for Integrative and Experimental Genomics), Gunnar Nilsson(Karolinska University Hospital), Andreas Reiter(Heidelberg University), Olivier Hermine(Délégation Paris 5), Karl Sotlar(Paracelsus Medical University), Wolfgang R. Sperr(Ludwig Boltzmann Institute for Cardiovascular Research), Luís Escribano(Centro de Investigación del Cáncer), Tracy I. George(University of New Mexico), Hanneke C. Kluin‐Nelemans(University Medical Center Groningen), Celalettin Üstün(University of Minnesota), Massimo Triggiani(University of Salerno), Knut Brockow(Technical University of Munich), Jason Gotlib(Stanford University), Alberto Órfão(Centro de Investigación del Cáncer), Lawrence B. Schwartz(Virginia Commonwealth University), Sigurd Broesby‐Olsen(Odense University Hospital), Carsten Bindslev‐Jensen(Odense University Hospital), Petri T. Kovanen(Wihuri Research Institute), Stephen J. Galli(University of Illinois Chicago), K. Frank Austen(Brigham and Women's Hospital), Daniel A. Arber(University of Illinois Chicago), Hans-Peter Horny(Ludwig-Maximilians-Universität München), Michel Arock(École Normale Supérieure Paris-Saclay), Dean D. Metcalfe(National Institute of Allergy and Infectious Diseases)
Cancer Research
March 2, 2017
Cited by 247Open Access
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Abstract

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.


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