Clinical and cytologic characteristics were correlated to immunologic
markersin 154 patients with newly diagnosed acute myeloid leukemia (AM
L). The panel of monoclonal antibodies (MoAbs) was selected to identif
y differentiation-associated antigens of both the myeloid and the lymp
hoid lineages (CD13, CD33, CD14, CD15, CD7, CD34, CD10, HLA-DR, CD19,
CD2, CD5, TdT). The expression of multidrug resistance P-glycoprotein
(P-170) was also evaluated in 117 patients. Differences in antigenic e
xpression was observed among the various French-American-British (FAB)
subgroups. HLA-DR was poorly expressed on the blasts of acutepromyelo
cytic leukemia (M3), and was always found in FAB M5. CD34 was detectab
le in all MO cases and only in one M3 (p < 0.001). Lymphoid-associated
antigens were positive in 74 cases (48.1%). In particular, CD7 was fo
und in 49 patients (31.8%), and TdT in 30 (21.3%), 15 samples displayi
ng coexpression of these two antigens. The incidence of CD7+ cases was
particularly elevated in MO and M5 AML (p = 0.005). It significantly
correlated with the expression of CD34,HLA-DR, P-170 (p < 0.001, p = 0
.018 and p = 0.034 respectively), and with a leukocyte count > 50 x 10
(9)/I (p = 0.038). Sixty-nine (59%) samples demonstrated P-170 positiv
ity. Again, this phenotype was particularly expressedin the poorly dif
ferentiated forms (M5, M0 and M1) and showed significant correlation w
ith the immaturity markers CD34, CD7 and HLA-DR (p = 0.013, p = 0.022
and p = .001, respectively). Expression of individual antigens correla
ted with prognosis. Refractoriness to first line therapy was associate
d with CD7 expression (p = 0.002) and P-170 (p = 0.001). The CD7 marke
r was also significantly associated with a very low overall survival (
p < 0.001) and continuous complete remission (p < 0.001). CD14 express
ion also significantly predicted lowersurvival rates (p = 0.033). The
combination (CD7+ CD14+) identified a subset of patients with a partic
ularly adverse outcome. The prognostic value of CD7 expression, alone
or in combination with other markers, was confirmed in multivariate an
alysis.