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Mastocytosis: 2016 updated WHO classification and novel emerging treatment concepts
Abstract
Over the past few years, substantial advances have been made in understanding the pathogenesis, evolution, and complexity of mast cell neoplasms. New diagnostic and prognostic parameters and novel therapeutic targets with demonstrable clinical impact have been identified. Several of these new markers, molecular targets, and therapeutic approaches have been validated and translated into clinical practice. At the same time, the classification of mastocytosis and related diagnostic criteria have been refined and updated by the consensus group and the World Health Organization (WHO). As a result, more specific therapies tailored toward prognostic subgroups of patients have been developed. Emerging treatment concepts use drugs directed against KIT and other relevant targets in neoplastic mast cells and will hopefully receive recognition by health authorities in the near future. This article provides an overview of recent developments in the field, with emphasis on the updated WHO classification, refined criteria, additional prognostic parameters, and novel therapeutic approaches. Based on these emerging concepts, the prognosis, quality of life, and survival of patients with advanced mastocytosis are expected to improve in the coming years.
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“Most cases are benign, but mastocytosis can also be associated with other hematological malignancies, 138 or can itself become malignant.”
From Mast cell ontogeny: From fetal development to life‐long health and disease (2023) · cites this paper as [138]
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Arber, D. A., Orazi, A., Hasserjian, R., Thiele, J., Borowitz, M. J., Le Beau, M. M., Bloomfield, C. D., Cazzola, M., & Vardiman, J. W. (2016) · Blood · doi:10.1182/blood-2016-03-643544 · Cited by 10,119
Valent, P., Akin, C., Escribano, L., Födinger, M., Hartmann, K., Brockow, K., Castells, M., Sperr, W. R., Kluin‐Nelemans, H. C., Hamdy, N. A. T., et al. (2007) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2007.01807.x · Cited by 750 · cited 10×
“Based on previous classification proposals and the classification of the World Health Organization (WHO), mastocytosis can be divided into subvariants of cutaneous mastocytosis (CM), in which no systemic involvement is found, systemic variants (SM), and localized MC tumors.(1,6-11) Historically, mastocytosis was first…”
BackgroundMethodResultInfluentialSelf-citationMast Cells, Mastocytosis, and Related Disorders
Theoharides, T. C., Valent, P., & Akin, C. (2015) · New England Journal of Medicine · doi:10.1056/nejmra1409760 · Cited by 518
Self-citationBodemer, C., Hermine, O., Palmérini, F., Yang, Y., Grandpeix-Guyodo, C., Leventhal, P. S., Hadj-Rabia, S., Nasca, L., Georgin-Lavialle, S., Cohen-Akenine, A., et al. (2010) · Journal of Investigative Dermatology · doi:10.1038/jid.2009.281 · Cited by 397
Peter, B., Winter, G. E., Blatt, K., Bennett, K. L., Stefanzl, G., Rix, U., Eisenwort, G., Hadzijusufovic, E., Gridling, M., Dutreix, C., et al. (2016) · Leukemia · doi:10.1038/leu.2015.242 · Cited by 63
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Research works printed but not linked: 95
- Parwaresch, 1985, Tissue mast cells in health and disease, Pathol Res Pract, 179, 439, 10.1016/S0344-0338(85)80184-9 · DOI
- Valent, 2003, Diagnosis and treatment of systemic mastocytosis: state of the art, Br J Haematol, 122, 695, 10.1046/j.1365-2141.2003.04575.x · DOI
- Metcalfe, 2008, Mast cells and mastocytosis, Blood, 112, 946, 10.1182/blood-2007-11-078097 · DOI · Paper page
- Horny, 1985, Bone marrow findings in systemic mastocytosis, Hum Pathol, 16, 808, 10.1016/S0046-8177(85)80252-5 · DOI
- Horny, 2001, Diagnosis of mastocytosis: general histopathological aspects, morphological criteria, and immunohistochemical findings, Leuk Res, 25, 543, 10.1016/S0145-2126(01)00021-2 · DOI
- Metcalfe, 1991, Classification and diagnosis of mastocytosis: current status, J Invest Dermatol, 96, 2S, 10.1111/1523-1747.ep12468882 · DOI
- Valent, 1996, Biology, classification and treatment of human mastocytosis, Wien Klin Wochenschr, 108, 385
- Valent, 2001, Diagnostic criteria and classification of mastocytosis: a consensus proposal, Leuk Res, 25, 603, 10.1016/S0145-2126(01)00038-8 · DOI
- Nettleship, 1869, Rare forms of urticaria, Br Med J, 2, 323
- Ellis, 1949, Urticaria pigmentosa; a report of a case with autopsy, Arch Pathol (Chic), 48, 426
- Caplan, 1963, The natural course of urticaria pigmentosa. Analysis and follow-up of 112 cases, Arch Dermatol, 87, 146, 10.1001/archderm.1963.01590140008002 · DOI
- Escribano, 2002, Mastocytosis: current concepts in diagnosis and treatment, Ann Hematol, 81, 677, 10.1007/s00277-002-0575-z · DOI
- Arock, 2010, Pathogenesis, classification and treatment of mastocytosis: state of the art in 2010 and future perspectives, Expert Rev Hematol, 3, 497, 10.1586/ehm.10.42 · DOI
- Nagata, 1995, Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder, Proc Natl Acad Sci USA, 92, 10560, 10.1073/pnas.92.23.10560 · DOI
- Longley, 1996, Somatic c-KIT activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm, Nat Genet, 12, 312, 10.1038/ng0396-312 · DOI
- Fritsche-Polanz, 2001, Mutation analysis of C-KIT in patients with myelodysplastic syndromes without mastocytosis and cases of systemic mastocytosis, Br J Haematol, 113, 357, 10.1046/j.1365-2141.2001.02783.x · DOI
- Horny, 1998, Diagnostic value of immunostaining for tryptase in patients with mastocytosis, Am J Surg Pathol, 22, 1132, 10.1097/00000478-199809000-00013 · DOI
- Escribano, 1998, Indolent systemic mast cell disease in adults: immunophenotypic characterization of bone marrow mast cells and its diagnostic implications, Blood, 91, 2731, 10.1182/blood.V91.8.2731.2731_2731_2736 · DOI
- Schwartz, 2000, Serum tryptase and the laboratory diagnosis of systemic mastocytosis, Hematol Oncol Clin North Am, 14, 641, 10.1016/S0889-8588(05)70300-2 · DOI
- Sperr, 2001, Morphologic properties of neoplastic mast cells: delineation of stages of maturation and implication for cytological grading of mastocytosis, Leuk Res, 25, 529, 10.1016/S0145-2126(01)00041-8 · DOI
- Valent, 1999, Recent advances in mastocytosis research. Summary of the Vienna Mastocytosis Meeting 1998, Int Arch Allergy Immunol, 120, 1, 10.1159/000024214 · DOI
- Hartmann, 2016, Cutaneous manifestations in patients with mastocytosis: consensus report of the European Competence Network on Mastocytosis; the American Academy of Allergy, Asthma & Immunology; and the European Academy of Allergology and Clinical Immunology, J Allergy Clin Immunol, 137, 35, 10.1016/j.jaci.2015.08.034 · DOI
- Valent, 2014, Refined diagnostic criteria and classification of mast cell leukemia (MCL) and myelomastocytic leukemia (MML): a consensus proposal, Ann Oncol, 25, 1691, 10.1093/annonc/mdu047 · DOI
- Lim, 2009, Systemic mastocytosis in 342 consecutive adults: survival studies and prognostic factors, Blood, 113, 5727, 10.1182/blood-2009-02-205237 · DOI
- Escribano, 2009, Prognosis in adult indolent systemic mastocytosis: a long-term study of the Spanish Network on Mastocytosis in a series of 145 patients, J Allergy Clin Immunol, 124, 514, 10.1016/j.jaci.2009.05.003 · DOI
- Pardanani, 2009, Prognostically relevant breakdown of 123 patients with systemic mastocytosis associated with other myeloid malignancies, Blood, 114, 3769, 10.1182/blood-2009-05-220145 · DOI
- Pardanani, 2010, WHO subvariants of indolent mastocytosis: clinical details and prognostic evaluation in 159 consecutive adults, Blood, 115, 150, 10.1182/blood-2009-10-249979 · DOI
- Travis, 1986, Mast cell leukemia: report of a case and review of the literature, Mayo Clin Proc, 61, 957, 10.1016/S0025-6196(12)62636-6 · DOI
- Valent, 2015, Chronic mast cell leukemia: a novel leukemia-variant with distinct morphological and clinical features, Leuk Res, 39, 1, 10.1016/j.leukres.2014.09.010 · DOI
- Arock, 2015, KIT mutation analysis in mast cell neoplasms: recommendations of the European Competence Network on Mastocytosis, Leukemia, 29, 1223, 10.1038/leu.2015.24 · DOI · Paper page
- Mayerhofer, 2008, Unique effects of KIT D816V in BaF3 cells: induction of cluster formation, histamine synthesis, and early mast cell differentiation antigens, J Immunol, 180, 5466, 10.4049/jimmunol.180.8.5466 · DOI
- Zappulla, 2005, Mastocytosis in mice expressing human Kit receptor with the activating Asp816Val mutation, J Exp Med, 202, 1635, 10.1084/jem.20050807 · DOI
- Ma, 2002, The c-KIT mutation causing human mastocytosis is resistant to STI571 and other KIT kinase inhibitors; kinases with enzymatic site mutations show different inhibitor sensitivity profiles than wild-type kinases and those with regulatory-type mutations, Blood, 99, 1741, 10.1182/blood.V99.5.1741 · DOI
- Akin, 2003, Effects of tyrosine kinase inhibitor STI571 on human mast cells bearing wild-type or mutated c-kit, Exp Hematol, 31, 686, 10.1016/S0301-472X(03)00112-7 · DOI
- Akin, 2004, A novel form of mastocytosis associated with a transmembrane c-kit mutation and response to imatinib, Blood, 103, 3222, 10.1182/blood-2003-11-3816 · DOI · Paper page
- Zhang, 2006, A novel K509I mutation of KIT identified in familial mastocytosis-in vitro and in vivo responsiveness to imatinib therapy, Leuk Res, 30, 373, 10.1016/j.leukres.2005.08.015 · DOI · Paper page
- Alvarez-Twose, 2012, Complete response after imatinib mesylate therapy in a patient with well-differentiated systemic mastocytosis, J Clin Oncol, 30, e126, 10.1200/JCO.2011.38.9973 · DOI
- de Melo Campos, 2014, Familial systemic mastocytosis with germline KIT K509I mutation is sensitive to treatment with imatinib, dasatinib and PKC412, Leuk Res, 38, 1245, 10.1016/j.leukres.2014.07.010 · DOI
- Harir, 2008, Oncogenic Kit controls neoplastic mast cell growth through a Stat5/PI3-kinase signaling cascade, Blood, 112, 2463, 10.1182/blood-2007-09-115477 · DOI
- Blatt, 2012, The PI3-kinase/mTOR-targeting drug NVP-BEZ235 inhibits growth and IgE-dependent activation of human mast cells and basophils, PLoS One, 7, e29925, 10.1371/journal.pone.0029925 · DOI
- Gabillot-Carré, 2006, Rapamycin inhibits growth and survival of D816V-mutated c-kit mast cells, Blood, 108, 1065, 10.1182/blood-2005-06-2433 · DOI
- Baumgartner, 2009, Expression of activated STAT5 in neoplastic mast cells in systemic mastocytosis: subcellular distribution and role of the transforming oncoprotein KIT D816V, Am J Pathol, 175, 2416, 10.2353/ajpath.2009.080953 · DOI
- Voisset, 2007, The tyrosine kinase FES is an essential effector of KITD816V proliferation signal, Blood, 110, 2593, 10.1182/blood-2007-02-076471 · DOI
- Parikh, 2010, Experience with everolimus (RAD001), an oral mammalian target of rapamycin inhibitor, in patients with systemic mastocytosis, Leuk Lymphoma, 51, 269, 10.3109/10428190903486220 · DOI
- Traina, 2012, Single nucleotide polymorphism array lesions, TET2, DNMT3A, ASXL1 and CBL mutations are present in systemic mastocytosis, PLoS One, 7, e43090, 10.1371/journal.pone.0043090 · DOI
- Wilson, 2011, Clonal analysis of NRAS activating mutations in KIT-D816V systemic mastocytosis, Haematologica, 96, 459, 10.3324/haematol.2010.031690 · DOI
- Schwaab, 2013, Comprehensive mutational profiling in advanced systemic mastocytosis, Blood, 122, 2460, 10.1182/blood-2013-04-496448 · DOI
- Damaj, 2014, ASXL1 but not TET2 mutations adversely impact overall survival of patients suffering systemic mastocytosis with associated clonal hematologic non-mast-cell diseases, PLoS One, 9, e85362, 10.1371/journal.pone.0085362 · DOI
- Gleixner, 2011, KIT-D816V-independent oncogenic signaling in neoplastic cells in systemic mastocytosis: role of Lyn and Btk activation and disruption by dasatinib and bosutinib, Blood, 118, 1885, 10.1182/blood-2010-06-289959 · DOI
- Sotlar, 2008, Systemic mastocytosis associated with chronic idiopathic myelofibrosis: a distinct subtype of systemic mastocytosis associated with a clonal hematological non-mast cell lineage disorder carrying the activating point mutations KITD816V and JAK2V617F, J Mol Diagn, 10, 58, 10.2353/jmoldx.2008.070061 · DOI
- Broesby-Olsen, 2012, Adult-onset systemic mastocytosis in monozygotic twins with KIT D816V and JAK2 V617F mutations, J Allergy Clin Immunol, 130, 806, 10.1016/j.jaci.2012.04.013 · DOI
- Ghanim, 2012, 5-azacytidine and decitabine exert proapoptotic effects on neoplastic mast cells: role of FAS-demethylation and FAS re-expression, and synergism with FAS-ligand, Blood, 119, 4242, 10.1182/blood-2011-09-382770 · DOI
- Wedeh, 2015, Identification of bromodomain-containing protein-4 as a novel marker and epigenetic target in mast cell leukemia, Leukemia, 29, 2230, 10.1038/leu.2015.138 · DOI
- Aichberger, 2007, Identification of MCL1 as a novel target in neoplastic mast cells in systemic mastocytosis: inhibition of mast cell survival by MCL1 antisense oligonucleotides and synergism with PKC412, Blood, 109, 3031, 10.1182/blood-2006-07-032714 · DOI
- Fumo, 2004, 17-Allylamino-17-demethoxygeldanamycin (17-AAG) is effective in down-regulating mutated, constitutively activated KIT protein in human mast cells, Blood, 103, 1078, 10.1182/blood-2003-07-2477 · DOI
- Kondo, 2007, Identification of heat shock protein 32 (Hsp32) as a novel survival factor and therapeutic target in neoplastic mast cells, Blood, 110, 661, 10.1182/blood-2006-10-054411 · DOI
- Santos, 2006, CD52 is expressed on human mast cells and is a potential therapeutic target in Waldenstrom’s macroglobulinemia and mast cell disorders, Clin Lymphoma Myeloma, 6, 478, 10.3816/CLM.2006.n.029 · DOI
- Krauth, 2007, Effects of the CD33-targeted drug gemtuzumab ozogamicin (Mylotarg) on growth and mediator secretion in human mast cells and blood basophils, Exp Hematol, 35, 108, 10.1016/j.exphem.2006.09.008 · DOI
- Sotlar, 2011, Aberrant expression of CD30 in neoplastic mast cells in high-grade mastocytosis, Mod Pathol, 24, 585, 10.1038/modpathol.2010.224 · DOI
- Morgado, 2013, CD30 expression by bone marrow mast cells from different diagnostic variants of systemic mastocytosis, Histopathology, 63, 780, 10.1111/his.12221 · DOI
- Hoermann, 2014, CD52 is a molecular target in advanced systemic mastocytosis, FASEB J, 28, 3540, 10.1096/fj.14-250894 · DOI
- Blatt, 2015, Identification of the Ki-1 antigen (CD30) as a novel therapeutic target in systemic mastocytosis, Blood, 126, 2832, 10.1182/blood-2015-03-637728 · DOI
- Pardanani, 2015, Aberrant expression of CD123 (interleukin-3 receptor-α) on neoplastic mast cells, Leukemia, 29, 1605, 10.1038/leu.2015.16 · DOI
- Jeong, 2007, Successful treatment of systemic mastocytosis associated with AML-M2, t(8:21) in a child using MRC-based AML chemotherapy along with gemtuzumab, J Allergy Clin Immunol, 119, 207
- Alvarez-Twose, 2016, Complete response to gemtuzumab ozogamicin in a patient with refractory mast cell leukemia, Leukemia, 30, 1753, 10.1038/leu.2016.30 · DOI
- Rabenhorst, 2016, Expression of programmed cell death ligand-1 in mastocytosis correlates with disease severity, J Allergy Clin Immunol, 137, 314, 10.1016/j.jaci.2015.07.006 · DOI
- Valent, 2011, Targeting of leukemia-initiating cells to develop curative drug therapies: straightforward but nontrivial concept, Curr Cancer Drug Targets, 11, 56, 10.2174/156800911793743655 · DOI
- Pelosi, 2015, Targeting LSCs through membrane antigens selectively or preferentially expressed on these cells, Blood Cells Mol Dis, 55, 336, 10.1016/j.bcmd.2015.07.015 · DOI
- Eisenwort, 2014, Identification of a neoplastic stem cell in human mast cell leukemia, Blood, 124, 817, 10.1182/blood.V124.21.817.817 · DOI
- Kluin-Nelemans, 1992, Response to interferon alfa-2b in a patient with systemic mastocytosis, N Engl J Med, 326, 619, 10.1056/NEJM199202273260907 · DOI
- Casassus, 2002, Treatment of adult systemic mastocytosis with interferon-alpha: results of a multicentre phase II trial on 20 patients, Br J Haematol, 119, 1090, 10.1046/j.1365-2141.2002.03944.x · DOI
- Lim, 2009, Cytoreductive therapy in 108 adults with systemic mastocytosis: Outcome analysis and response prediction during treatment with interferon-alpha, hydroxyurea, imatinib mesylate or 2-chlorodeoxyadenosine, Am J Hematol, 84, 790, 10.1002/ajh.21561 · DOI
- Kluin-Nelemans, 2003, Cladribine therapy for systemic mastocytosis, Blood, 102, 4270, 10.1182/blood-2003-05-1699 · DOI
- Barete, 2015, Long-term efficacy and safety of cladribine (2-CdA) in adult patients with mastocytosis, Blood, 126, 1009, 10.1182/blood-2014-12-614743 · DOI
- Ustun, 2014, Hematopoietic stem-cell transplantation for advanced systemic mastocytosis, J Clin Oncol, 32, 3264, 10.1200/JCO.2014.55.2018 · DOI
- Ustun, 2016, Consensus opinion on allogeneic hematopoietic cell transplantation in advanced systemic mastocytosis, Biol Blood Marrow Transplant, 22, 1348, 10.1016/j.bbmt.2016.04.018 · DOI
- Fabbro, 2000, PKC412--a protein kinase inhibitor with a broad therapeutic potential, Anticancer Drug Des, 15, 17
- Ustun, 2011, Tyrosine kinase inhibitors in the treatment of systemic mastocytosis, Leuk Res, 35, 1143, 10.1016/j.leukres.2011.05.006 · DOI
- Growney, 2005, Activation mutations of human c-KIT resistant to imatinib mesylate are sensitive to the tyrosine kinase inhibitor PKC412, Blood, 106, 721, 10.1182/blood-2004-12-4617 · DOI
- Gleixner, 2006, PKC412 inhibits in vitro growth of neoplastic human mast cells expressing the D816V-mutated variant of KIT: comparison with AMN107, imatinib, and cladribine (2CdA) and evaluation of cooperative drug effects, Blood, 107, 752, 10.1182/blood-2005-07-3022 · DOI
- Gotlib, 2005, Activity of the tyrosine kinase inhibitor PKC412 in a patient with mast cell leukemia with the D816V KIT mutation, Blood, 106, 2865, 10.1182/blood-2005-04-1568 · DOI
- Krauth, 2009, Midostaurin (PKC412) inhibits immunoglobulin E-dependent activation and mediator release in human blood basophils and mast cells, Clin Exp Allergy, 39, 1711, 10.1111/j.1365-2222.2009.03353.x · DOI
- Gotlib, 2016, Efficacy and safety of midostaurin in advancedsystemic mastocytosis, N Engl J Med, 374, 2530, 10.1056/NEJMoa1513098 · DOI
- Chandesris, 2016, Midostaurin in advanced systemic mastocytosis, N Engl J Med, 374, 2605, 10.1056/NEJMc1515403 · DOI
- Gotlib, 2013, Durable responses and improved quality of life with midostaurin (PKC412) in advanced systemic mastocytosis (SM): updated stage 1 results of the global D2201 trial, Blood, 122, 106, 10.1182/blood.V122.21.106.106 · DOI
- Vega-Ruiz, 2009, Phase II study of imatinib mesylate as therapy for patients with systemic mastocytosis, Leuk Res, 33, 1481, 10.1016/j.leukres.2008.12.020 · DOI
- Paul, 2010, Masitinib for the treatment of systemic and cutaneous mastocytosis with handicap: a phase 2a study, Am J Hematol, 85, 921, 10.1002/ajh.21894 · DOI
- Hochhaus, 2015, Nilotinib in patients with systemic mastocytosis: analysis of the phase 2, open-label, single-arm nilotinib registration study, J Cancer Res Clin Oncol, 141, 2047, 10.1007/s00432-015-1988-0 · DOI
- Alvarez-Twose, Imatinib in systemic mastocytosis: a phase IV clinical trial in patients lacking exon 17 KIT mutations and review of the literature [published online ahead of print 19 July 2016], Oncotarget
- Pardanani, 2013, How I treat patients with indolent and smoldering mastocytosis (rare conditions but difficult to manage), Blood, 121, 3085, 10.1182/blood-2013-01-453183 · DOI · Paper page
- Arock, 2015, Current treatment options in patients with mastocytosis: status in 2015 and future perspectives, Eur J Haematol, 94, 474, 10.1111/ejh.12544 · DOI
- Valent, 2010, How I treat patients with advanced systemic mastocytosis, Blood, 116, 5812, 10.1182/blood-2010-08-292144 · DOI
- Wimazal, 2012, Severe life-threatening or disabling anaphylaxis in patients with systemic mastocytosis: a single-center experience, Int Arch Allergy Immunol, 157, 399, 10.1159/000329218 · DOI
- Valent, 2003, Aggressive systemic mastocytosis and related mast cell disorders: current treatment options and proposed response criteria, Leuk Res, 27, 635, 10.1016/S0145-2126(02)00168-6 · DOI
- Gotlib, 2013, International Working Group-Myeloproliferative Neoplasms Research and Treatment (IWG-MRT) & European Competence Network on Mastocytosis (ECNM) consensus response criteria in advanced systemic mastocytosis, Blood, 121, 2393, 10.1182/blood-2012-09-458521 · DOI
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Metadata
- Authors
- Valent, P., Akin, C., & Metcalfe, D. D.
- Affiliations
- Division of Hematology & Hemostaseology and Ludwig Boltzmann Cluster Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria;
- Division of Allergy and Immunology, Department of Medicine, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA; and
- Mast Cell Biology Section, Laboratory of Allergic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2017-03-16
- Volume
- 129
- Issue
- 11
- Pages
- 1420-1427
- ISSN
- 0006-4971
- 1528-0020
- Cited by
- 592
- References
- 5
- Language
- en
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