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. 2008 Oct 7;113(1):154–164. doi: 10.1182/blood-2007-10-119438

Table 1.

Demographics and clinical characteristics of the 256 newly diagnosed AML patients in the study set

Variable category Number or %
No. of cases 256
% male 53.8%
Race
    Asian 1.9%
    Black 8.3%
    Hispanic 12.8%
    White 76.7%
Age, y
    Mean 61.1
    Median 63.8
    Minimum 16.1
    Maximum 87.2
FAB
    M0 6.5%
    M1 13.8%
    M2 26.8%
    M4 23.4%
    M4EOS 3.4%
    M5 2.3%
    M5A 5.4%
    M5b 3.8%
    M6 2.7%
    M7 1.9%
    RAEBT 1.9%
    Unknown 8.0%
WHO classification
    AML with recurrent cytogenetic changes 29
    AML with multilineage dysplasia 59
    AML, therapy related 36
    AML not otherwise categorized 134
Cytogenetics
    Favorable 8.3%
    Intermediate 45.7%
    Unfavorable 44.5%
    ND 1.5%
Zubrod PS
    0-2 94.1%
    3 or 4 5.9%
AHD
    ≥ 2 mo 32.1%
Response
    CR 56.8%
    CRP 3.2%
    Early death 0.5%
    Fail 8.1%
    Resistant 31.1%
    Inevaluable 0.5%
Relapse
    Yes 54.1%
Alive
    Yes 29.4%

RAEBT indicates refractory anemia with excess of blasts in transformation; AML, acute myeloid leukemia; AHD ≥ 2, antecedent hematologic disorder of greater than or equal to 2 months; CR, complete remission; CRp, complete remission criteria met except that platelets fail to reach 100 000 μL; Early death, death within the first 2 weeks after the start of induction therapy; and Fail, death occurring more than 2 weeks after the start of therapy.