How I treat paroxysmal nocturnal hemoglobinuria

被引:157
作者
Brodsky, Robert A. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Med, Div Hematol, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
COMPLEMENT INHIBITOR ECULIZUMAB; PIG-A; NATURAL-HISTORY; APLASTIC-ANEMIA; CELLS; TRANSPLANTATION; GRANULOCYTES; PHENOTYPE; MECHANISM; CYCLOPHOSPHAMIDE;
D O I
10.1182/blood-2009-03-195966
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal blood disorder that manifests with hemolytic anemia, bone marrow failure, and thrombosis. Many of the clinical manifestations of the disease result from complement-mediated intravascular hemolysis. Allogeneic bone marrow transplantation is the only curative therapy for PNH. Eculizumab, a monoclonal antibody that blocks terminal complement activation, is highly effective in reducing hemolysis, improving quality of life, and reducing the risk for thrombosis in PNH patients. Insights into the relevance of detecting PNH cells in PNH and other bone marrow failure disorders are highlighted, and indications for treating PNH patients with bone marrow transplantation and eculizumab are explored. (Blood. 2009; 113: 6522-6527)
引用
收藏
页码:6522 / 6527
页数:6
相关论文
共 54 条
  • [1] ANTIN JH, 1985, BLOOD, V66, P1247
  • [2] Clonal populations of hematopoietic cells with paroxysmal nocturnal hemoglobinuria genotype and phenotype are present in normal individuals
    Araten, DJ
    Nafa, K
    Pakdeesuwan, K
    Luzzatto, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (09) : 5209 - 5214
  • [3] BESSLER M, 1991, EUR J HAEMATOL, V47, P179
  • [4] Reduced intensity HLA-haploidentical BMT with post transplantation cyclophosphamide in nonmalignant hematologic diseases
    Brodsky, R. A.
    Luznik, L.
    Bolanos-Meade, J.
    Leffell, M. S.
    Jones, R. J.
    Fuchs, E. J.
    [J]. BONE MARROW TRANSPLANTATION, 2008, 42 (08) : 523 - 527
  • [5] Resistance of paroxysmal nocturnal hemoglobinuria cells to the glycosylphosphatidylinositol-binding toxin aerolysin
    Brodsky, RA
    Mukhina, GL
    Nelson, KL
    Lawrence, TS
    Jones, RJ
    Buckley, JT
    [J]. BLOOD, 1999, 93 (05) : 1749 - 1756
  • [6] Aplastic anaemia
    Brodsky, RA
    Jones, RJ
    [J]. LANCET, 2005, 365 (9471) : 1647 - 1656
  • [7] Improved detection and characterization of paroxysmal nocturnal hemoglobinuria using fluorescent aerolysin
    Brodsky, RA
    Mukhina, GL
    Li, SY
    Nelson, KL
    Chiurazzi, PL
    Buckley, JT
    Borowitz, MJ
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 114 (03) : 459 - 466
  • [8] Brodsky RA, 2009, HEMATOLOGY BASIC PRI, P385
  • [9] Narrative review: Paroxysmal nocturnal hemoglobinuria: The physiology of complement-related hemolytic anemia
    Brodsky, Robert A.
    [J]. ANNALS OF INTERNAL MEDICINE, 2008, 148 (08) : 587 - 595
  • [10] Multicenter phase 3 study of the complement inhibitor eculizumab for the treatment of patients with paroxysmal nocturnal hemoglobinuria
    Brodsky, Robert A.
    Young, Neal S.
    Antonioli, Elisabetta
    Risitano, Antonio M.
    Schrezenmeier, Hubert
    Schubert, Jorg
    Gaya, Anna
    Coyle, Luke
    De Castro, Carlos
    Fu, Chieh-Lin
    Maciejewski, Jaroslaw P.
    Bessler, Monica
    Kroon, Henk-Andre
    Rother, Russell P.
    Hillmen, Peter
    [J]. BLOOD, 2008, 111 (04) : 1840 - 1847