International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) & European Competence Network on Mastocytosis (ECNM) consensus response criteria in advanced systemic mastocytosis

Author:

Gotlib Jason1,Pardanani Animesh2,Akin Cem3,Reiter Andreas4,George Tracy1,Hermine Olivier5,Kluin-Nelemans Hanneke6,Hartmann Karin7,Sperr Wolfgang R.8,Brockow Knut9,Schwartz Lawrence B.10,Orfao Alberto11,DeAngelo Daniel J.12,Arock Michel13,Sotlar Karl14,Horny Hans-Peter14,Metcalfe Dean D.15,Escribano Luis11,Verstovsek Srdan16,Tefferi Ayalew2,Valent Peter8

Affiliation:

1. Stanford University School of Medicine, Stanford, CA;

2. Mayo Clinic, Rochester, MN;

3. Harvard Medical School and Brigham and Women’s Hospital, Boston, MA;

4. III. Medizinische Klinik, Universitätsmedizin Mannheim, Mannheim, Germany;

5. Centre National de Recherche Scientifique Unité Mixte de Recherche 8147 and Necker Hospital, Paris Descartes University, Paris, France;

6. University Medical Centre Groningen, Groningen, The Netherlands;

7. University of Cologne, Cologne, Germany;

8. Medical University of Vienna, Vienna, Austria;

9. Biederstein Technical University, Munich, Germany;

10. Virginia Commonwealth University, Richmond, VA;

11. Universidad de Salamanca, Salamanca, Spain;

12. Dana Farber Cancer Institute, Boston, MA;

13. Laboratoire Central d’Hématologie, Groupe Hospitalier Pitié-Salpêtrière (Paris), and LBPA, CNRS UMR 8113, Ecole Normale Supérieure de Cachan, Cachan, France;

14. Ludwig-Maximilian University of Munich, Munich, Germany;

15. National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD;

16. MD Anderson Cancer Center, Houston, TX

Abstract

Abstract Systemic mastocytosis (SM) is characterized by accumulation of neoplastic mast cells and is classified into indolent and aggressive forms. The latter include aggressive SM (ASM), mast cell leukemia (MCL), and SM associated with a myeloid neoplasm wherein 1 or both disease compartments exhibit advanced features. These variants, henceforth collectively referred to as advanced SM for the purposes of this report, are typically characterized by organ damage and shortened survival duration. In contrast to indolent SM, in which symptoms are usually managed by noncytotoxic antimediator therapy, cytoreduction is usually necessary for disease control in advanced SM. Unfortunately, current drug treatment of these patients rarely results in complete clinical and histopathologic remissions or improved survival time. Previously defined response criteria were adapted to the heterogeneous presentations of advanced SM and the limited effects of available drugs. However, recent advances in understanding the molecular pathogenesis of SM and the corresponding prospect in targeted therapy make it a priority to modify these criteria. Our current study is the product of an international group of experts and summarizes the challenges in accomplishing this task and forwards a new proposal for response criteria, which builds on prior proposals and should facilitate response evaluation in clinical trials.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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