Thromboembolism in children with acute lymphoblastic leukaemia treated on Dana-Farber Cancer Institute protocols: effect of age and risk stratification of disease

被引:69
作者
Athale, UH
Siciliano, SA
Crowther, M
Barr, RD
Chan, AKC
机构
[1] McMaster Univ, Dept Pediat, HSC, Div Hematol Oncol, Hamilton, ON L8N 3Z5, Canada
[2] Hamilton Hlth Sci Corp, Hematol Oncol Serv, McMaster Childrens Hosp, Hamilton, ON, Canada
[3] McMaster Univ, Div Hematol, Dept Med, Hamilton, ON L8N 3Z5, Canada
关键词
acute lymphoblastic leukaemia; thromboembolism; asparaginase; steroids;
D O I
10.1111/j.1365-2141.2005.05528.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Children with acute lymphoblastic leukaemia (ALL) are at increased risk for thromboembolism (TE). Identification of a susceptible population is crucial for effective thromboprophylaxis. However, the risk factors for ALL-associated TE are unclear. Concomitant asparaginase (ASP) and steroid therapy has been shown to increase the incidence of TE. Dana-Farber Cancer Institute (DFCI)-ALL protocols use a combination of ASP and steroids during the postinduction intensification phase when high-risk (HR) patients receive thrice the steroid-dose given to standard-risk (SR) patients. We studied prospectively assembled cohorts of children treated on two consecutive DFCI-ALL protocols to define the risk factors for symptomatic TE. Ten (11%) of 91 patients developed symptomatic TE; eight (seven HR) during intensification. Seven (44%) of 16 older patients (>= 10 years) compared with three of 75 (4%) younger patients developed TE (P < 0.0001). Nine of 35 (26%) HR and one of 56 (2%) SR patients developed TE (P = 0.0006). Gender, ALL-immunophenotype, steroid-type or ASP dosing schedule did not alter the risk but older age and HR-disease were factors predisposing to TE associated with DFCI-ALL protocols. Age-related risk may partly reflect the effect of ALL-risk stratification. Higher dose steroids combined with ASP may lead to an increased risk of TE in HR patients.
引用
收藏
页码:803 / 810
页数:8
相关论文
共 39 条
  • [1] ACQUIRED ANTITHROMBIN-III DEFICIENCY SECONDARY TO ASPARAGINASE THERAPY IN CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA
    ANDREW, M
    BROOKER, L
    MITCHELL, L
    [J]. BLOOD COAGULATION & FIBRINOLYSIS, 1994, 5 : S24 - S36
  • [2] Arruda VR, 1997, THROMB HAEMOSTASIS, V77, P818
  • [3] Thrombosis in children with acute lymphoblastic leukemia. Part II. Pathogenesis of thrombosis in children with acute lymphoblastic leukemia: effects of the disease and therapy
    Athale, UH
    Chan, AKC
    [J]. THROMBOSIS RESEARCH, 2003, 111 (4-5) : 199 - 212
  • [4] Thrombosis in children with acute lymphoblastic leukemia - Part I. Epidemiology of thrombosis in children with acute lymphoblastic leukemia
    Athale, UH
    Chan, AKC
    [J]. THROMBOSIS RESEARCH, 2003, 111 (03) : 125 - 131
  • [5] 4-AGENT INDUCTION AND INTENSIVE ASPARAGINASE THERAPY FOR TREATMENT OF CHILDHOOD ACUTE LYMPHOBLASTIC-LEUKEMIA
    CLAVELL, LA
    GELBER, RD
    COHEN, HJ
    HITCHCOCKBRYAN, S
    CASSADY, JR
    TARBELL, NJ
    BLATTNER, SR
    TANTRAVAHI, R
    LEAVITT, P
    SALLAN, SE
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (11) : 657 - 663
  • [6] Second induction in pediatric patients with recurrent acute lymphoid leukemia using DFCI-ALL protocols
    Dalle, JH
    Moghrabi, A
    Rousseau, P
    Leclerc, JM
    Barrette, S
    Bernstein, ML
    Champagne, D
    David, M
    Demers, J
    Duval, M
    Hume, H
    Meyer, P
    Champagne, MA
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2005, 27 (02) : 73 - 79
  • [7] VENOUS THROMBOEMBOLIC COMPLICATIONS IN CHILDREN
    DAVID, M
    ANDREW, M
    [J]. JOURNAL OF PEDIATRICS, 1993, 123 (03) : 337 - 346
  • [8] Prophylactic therapy with enoxaparin during L-asparaginase treatment in children with acute lymphoblastic leukemia
    Elhasid, R
    Lanir, N
    Sharon, R
    Ben Arush, MW
    Levin, C
    Postovsky, S
    Ben Barak, A
    Brenner, B
    [J]. BLOOD COAGULATION & FIBRINOLYSIS, 2001, 12 (05) : 367 - 370
  • [9] A CANDIDATE GENETIC RISK FACTOR FOR VASCULAR-DISEASE - A COMMON MUTATION IN METHYLENETETRAHYDROFOLATE REDUCTASE
    FROSST, P
    BLOM, HJ
    MILOS, R
    GOYETTE, P
    SHEPPARD, CA
    MATTHEWS, RG
    BOERS, GJH
    DENHEIJER, M
    KLUIJTMANS, LAJ
    VANDENHEUVEL, LP
    ROZEN, R
    [J]. NATURE GENETICS, 1995, 10 (01) : 111 - 113
  • [10] Guttormsen AB, 1998, CLIN CHEM, V44, P1987