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Proposed European Competence Network on Mastocytosis-American Initiative in Mast Cell Diseases (ECNM-AIM) Response Criteria in Advanced Systemic Mastocytosis.
Gotlib, Jason; Schwaab, Juliana; Shomali, William; George, Tracy I; Radia, Deepti H; Castells, Mariana; Carter, Melody C; Hartmann, Karin; Álvarez-Twose, Ivan; Brockow, Knut; Bonadonna, Patrizia; Hermine, Olivier; Niedoszytko, Marek; Hoermann, Gregor; Sperr, Wolfgang R; Elberink, Hanneke Oude; Siebenhaar, Frank; Butterfield, Joseph H; Ustun, Celalettin; Zanotti, Roberta; Triggiani, Massimo; Schwartz, Lawrence B; Lyons, Jonathan J; Orfao, Alberto; Sotlar, Karl; Horny, Hans-Peter; Arock, Michel; Metcalfe, Dean D; Akin, Cem; Lübke, Johannes; Valent, Peter; Reiter, Andreas.
Afiliação
  • Gotlib J; Stanford Cancer Institute/Stanford University School of Medicine, Stanford, Calif. Electronic address: jason.gotlib@stanford.edu.
  • Schwaab J; Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
  • Shomali W; Stanford Cancer Institute/Stanford University School of Medicine, Stanford, Calif.
  • George TI; Department of Pathology, University of Utah, Salt Lake City, Utah.
  • Radia DH; Department of Clinical Haematology, Guys and St Thomas' NHS Hospitals, London, United Kingdom.
  • Castells M; Division of Allergy and Immunology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Mass.
  • Carter MC; Mast Cell Biology Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
  • Hartmann K; Division of Allergy, Department of Dermatology, University Hospital Basel and University of Basel, Basel, Switzerland; Department of Biomedicine, University Hospital Basel and University of Basel, Switzerland.
  • Álvarez-Twose I; Instituto de Estudios de Mastocitosis de Castilla La Mancha and Centro de Investigación Biomédica en Red de Oncología (CIBERONC), Hospital Virgen del Valle, Toledo, Spain.
  • Brockow K; Department of Dermatology and Allergy Biederstein, School of Medicine, Technical University of Munich, Munich, Germany.
  • Bonadonna P; Allergy Unit, Verona University Hospital, Verona, Italy.
  • Hermine O; Imagine Institute Université de Paris, Sorbonne, INSERM U1163, Centre National de Référence des Mastocytoses, Hôpital Necker, Assistance Publique Hôpitaux de Paris, Paris, France.
  • Niedoszytko M; Department of Allergology, Medical University of Gdansk, Gdansk, Poland.
  • Hoermann G; MLL Munich Leukemia Laboratory, Munich, Germany; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria.
  • Sperr WR; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
  • Elberink HO; Department of Allergology, University Medical Center Groningen and GRIAC Research Institute, University of Groningen, Groningen, The Netherlands.
  • Siebenhaar F; Institute of Allergology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany; Department of Allergology and Immunology, Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Berlin, Germany.
  • Butterfield JH; Division of Allergic Diseases, Mayo Clinic, Rochester, Minn.
  • Ustun C; Department of Medicine, Division of Hematology, Oncology, and Cell Therapy, Coleman Foundation Blood and Marrow Transplant Center at Rush University Medical Center, Chicago, Ill.
  • Zanotti R; Section of Hematology, Multidisciplinary Outpatients Clinics for Mastocytosis, Department of Medicine, University Hospital of Verona, Verona, Italy.
  • Triggiani M; Division of Allergy and Clinical Immunology, University of Salerno, Salerno, Italy.
  • Schwartz LB; Department of Internal Medicine, Division of Rheumatology, Allergy, and Immunology, Virginia Commonwealth University, Richmond, Va.
  • Lyons JJ; Translational Allergic Immunopathology Unit, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
  • Orfao A; Servicio Central de Citometria (NUCLEUS), Instituto de Biología Molecular y Celular del Cáncer (IBMCC) Instituto Biosanitario de Salamanca, CIBERONC and Department of Medicine, University of Salamanca, Salamanca, Spain; Utah.
  • Sotlar K; Institute of Pathology, Paracelsus Medical University Salzburg, Salzburg, Austria.
  • Horny HP; Institute of Pathology, Ludwig-Maximilians-University, Munich, Germany.
  • Arock M; Department of Hematological Biology, Pitié-Salpêtrière Hospital, Pierre et Marie Curie University, Paris, France.
  • Metcalfe DD; Mast Cell Biology Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Md.
  • Akin C; Division of Allergy and Clinical Immunology, University of Michigan, Ann Arbor, Mich.
  • Lübke J; Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
  • Valent P; Ludwig Boltzmann Institute for Hematology and Oncology, Medical University of Vienna, Vienna, Austria; Department of Internal Medicine I, Division of Hematology and Hemostaseology, Medical University of Vienna, Vienna, Austria.
  • Reiter A; Department of Hematology and Oncology, University Hospital Mannheim, Heidelberg University, Mannheim, Germany.
J Allergy Clin Immunol Pract ; 10(8): 2025-2038.e1, 2022 08.
Article em En | MEDLINE | ID: mdl-35724948
ABSTRACT
Advanced systemic mastocytosis (AdvSM) is characterized by the presence of KIT D816V and other somatic mutations (eg, in SRSF2, ASXL1, and RUNX1) in 95% and 60% to 70% of patients, respectively. The biological and clinical consequences of AdvSM include multilineage involvement (eg, associated hematologic neoplasm) in 60% to 80% of patients, variable infiltration and damage (C-findings) of predominantly bone marrow and visceral organs through affected mast cell (MC) and non-MC lineages, and elevated levels of serum tryptase. Recently, the treatment landscape has substantially changed with the introduction of the multikinase/KIT inhibitor midostaurin and the selective KIT D816V inhibitor avapritinib. In this review, we discuss the evolution of AdvSM response criteria that have been developed to better capture clinical benefit (eg, improved responses and progression-free and overall survival). We propose refined response criteria from European Competence Network on Mastocytosis and American Initiative in Mast Cell Diseases investigators that use a tiered approach to segregate the effects of histopathologic (eg, bone marrow MC burden, tryptase), molecular (eg, KIT D816V variant allele frequency), clinical (eg, C-findings), and symptom response on long-term outcomes. These response criteria require evaluation in future prospective clinical trials of selective KIT inhibitors and other novel agents.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mastocitose / Mastocitose Sistêmica / Transtornos da Ativação de Mastócitos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Mastocitose / Mastocitose Sistêmica / Transtornos da Ativação de Mastócitos Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article