Epidemiology of myelofibrosis, essential thrombocythemia, and polycythemia vera in the European Union

被引:184
作者
Moulard, Odile [1 ]
Mehta, Jyotsna [2 ]
Fryzek, Jon [3 ]
Olivares, Robert [1 ]
Iqbal, Usman [2 ]
Mesa, Ruben A. [4 ]
机构
[1] Med Affairs, Oncol Global Evidence & Value Dev, Chilly Mazarin, France
[2] Sanofi, Med Affairs, Oncol Global Evidence & Value Dev, Cambridge, MA USA
[3] EpidStat Inst, Ann Arbor, MI USA
[4] Mayo Clin, Ctr Canc, Div Hematol & Med Oncol, Scottsdale, AZ 85259 USA
关键词
polycythemia vera; epidemiology; Europe; essential thrombocythemia; myelofibrosis; MYELOPROLIFERATIVE DISORDERS; SYSTEM; TRENDS; LIFE;
D O I
10.1111/ejh.12256
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Primary myelofibrosis (PMF), essential thrombocythemia (ET), and polycythemia vera (PV) are BCR ABL-negative myeloproliferative neoplasms (MPN). Published epidemiology data are scarce, and multiple sources are needed to assess the disease burden. Methods We assembled the most recent information available on the incidence and prevalence of myelofibrosis (MF), ET, and PV by conducting a structured and exhaustive literature review of the published peer-reviewed literature in EMBASE and by reviewing online documentation from disease registries and relevant health registries in European countries. The search was restricted to human studies written in English or French and published between January 1, 2000, and December 6, 2012. Results Eleven articles identified from EMBASE, three online hematology or oncology registries, and two Web-based databases or reports were used to summarize epidemiological estimates for MF, PV, and ET. The incidence rate of MF ranged from 0.1 per 100000 per year to 1 per 100000 per year. Among the various registries, the incidence of PV ranged from 0.4 per 100000 per year to 2.8 per 100000 per year, while the literature estimated the range of PV incidence to be 0.68 per 100000 to 2.6 per 100000 per year. The estimated incidence of ET was between 0.38 per 100000 per year and 1.7 per 100000 per year. While a few studies reported on the MPNs' prevalences, it is difficult to compare them as various types of prevalence were calculated (point prevalence vs. period prevalence) and standardization was made according to different populations (e.g., the world population and the European population). Conclusion There is a wide variation in both prevalence and incidence estimates observed across European data sources. Carefully designed studies, with standardized definitions of MPNs and complete ascertainment of patients including both primary and secondary MFs, should be conducted so that estimates of the population aimed to receive novel treatments for these neoplasms are better understood assist public health planning and provide valuable information about the burden of illness to policy makers, funding agencies, resource planners, healthcare insurers, and pharmaceutical manufacturers.
引用
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页码:289 / 297
页数:9
相关论文
共 29 条
  • [1] TRENDS IN THE INCIDENCE OF POLYCYTHEMIA-VERA AMONG OLMSTED COUNTY, MINNESOTA RESIDENTS, 1935-1989
    ANIA, BJ
    SUMAN, VJ
    SOBELL, JL
    CODD, MB
    SILVERSTEIN, MN
    MELTON, LJ
    [J]. AMERICAN JOURNAL OF HEMATOLOGY, 1994, 47 (02) : 89 - 93
  • [2] [Anonymous], QUELQ DONN ISS 5 PRE
  • [3] BERGLUND S, 1992, EUR J HAEMATOL, V48, P20
  • [4] MYELOFIBROSIS IN CHRONIC MYELOPROLIFERATIVE DISORDERS - INCIDENCE AMONG SUBTYPES ACCORDING TO THE HANNOVER CLASSIFICATION
    BUHR, T
    GEORGII, A
    CHORITZ, H
    [J]. PATHOLOGY RESEARCH AND PRACTICE, 1993, 189 (02) : 121 - 132
  • [5] New prognostic scoring system for primary myelofibrosis based on a study of the International Working Group for Myelofibrosis Research and Treatment
    Cervantes, Francisco
    Dupriez, Brigitte
    Pereira, Arturo
    Passamonti, Francesco
    Reilly, John T.
    Morra, Enrica
    Vannucchi, Alessandro M.
    Mesa, Ruben A.
    Demory, Jean-Loup
    Barosi, Giovanni
    Rumi, Elisa
    Tefferi, Ayalew
    [J]. BLOOD, 2009, 113 (13) : 2895 - 2901
  • [6] Significant increase in the apparent incidence of essential thrombocythemia related to new WHO diagnostic criteria: a population-based study
    Girodon, Francois
    Bonicelli, Gilles
    Schaeffer, Celine
    Mounier, Morgane
    Carillo, Serge
    Lafon, Ingrid
    Carli, Paule Marie
    Janoray, Ines
    Ferrant, Emmanuelle
    Maynadie, Marc
    [J]. HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (06): : 865 - 869
  • [7] A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
    James, C
    Ugo, V
    Le Couédic, JP
    Staerk, J
    Delhommeau, F
    Lacout, C
    Garçon, L
    Raslova, H
    Berger, R
    Bennaceur-Griscelli, A
    Villeval, JL
    Constantinescu, SN
    Casadevall, N
    Vainchenker, W
    [J]. NATURE, 2005, 434 (7037) : 1144 - 1148
  • [8] Incidence, clinical features and outcome of essential thrombocythaemia in a well defined geographical area
    Jensen, MK
    Brown, PD
    Nielsen, OJ
    Hasselbalch, HC
    [J]. EUROPEAN JOURNAL OF HAEMATOLOGY, 2000, 65 (02) : 132 - 139
  • [9] Trends in the incidence of chronic Philadelphia chromosome negative (Ph-) myeloproliferative disorders in the city of Goteborg, Sweden, during 1983-99
    Johansson, P
    Kutti, J
    Andréasson, B
    Safai-Kutti, S
    Vilén, L
    Wedel, H
    Ridell, B
    [J]. JOURNAL OF INTERNAL MEDICINE, 2004, 256 (02) : 161 - 165
  • [10] Le Guyader-Peyrou S, 2010, INCIDENCE SURVIE INC