A. Cuneo et al., CYTOGENETIC PROFILE OF MINIMALLY DIFFERENTIATED (FAB M0) ACUTE MYELOID-LEUKEMIA - CORRELATION WITH CLINICOBIOLOGIC FINDINGS, Blood, 85(12), 1995, pp. 3688-3694
Cytogenetic data were studied in 26 patients with de novo acute myeloi
d leukemia (AML) with minimal myeloid differentiation, corresponding t
o the M0 subtype of the French-American-British classification, in cor
relation with cytoimmunologic and clinical findings. Clonal abnormalit
ies were detected in 21 cases (80.7%), 12 of which had a complex karyo
type. Partial or total monosomy 5q and/or 7q was found, either as the
sole aberration or in all abnormal metaphases, in 11 patients; in 8 ca
ses, additional chromosome changes were present, including rearrangeme
nts involving 12p12-13 and 2p12-15 seen in 3 cases each. Five patients
had trisomy 13 as a possible primary chromosome change; in 5 cases, n
onrecurrent chromsome abnormalities were observed. Comparison of these
findings with chromosome data from 42 patients with AML-M1 shows that
abnormal karyotypes, complex karyotypes, unbalanced chromosome change
s (-5/5q- and/or -7/7q- and +13) were observed much more frequently in
AML-M0 than in AML-M1. Patients with abnormalities of chromosome 5 an
d/or 7 frequently showed trilineage myelodysplasia and low white blood
cell count. Despite their relatively young age, complete remission wa
s achieved in 4 of 11 patients only. Patients with +13 were elderly ma
les with frequent professional exposure to myelotoxic agents. Unlike p
atients with clonal abnormalities, most AML-M0 patients with normal ka
ryotype showed 1% to 2% peroxidase-positive blast cells at light micro
scopy and frequently achieved CR. It is concluded that (1) AML-M0 show
s a distinct cytogenetic profile, partially recalling that of therapy-
related AML, (2) different cytogenetic groups of AML-M0 can be ideniti
fied showing characteristic clinicobiologic features, and (3) chromoso
me rearrangements may partially account for the unfavorable outcome fr
equently observed in these patients. (C) 1995 by The American Society
of Hematology.