MINIMALLY DIFFERENTIATED ACUTE-LEUKEMIA

被引:7
作者
CADWELL, FJ
BURNS, CP
DICK, FR
JONES, MP
HECKMAN, KD
WEINER, GJ
GOEKEN, JA
机构
[1] UNIV IOWA, COLL MED, DEPT MED, IOWA CITY, IA 52242 USA
[2] UNIV IOWA, COLL MED, DEPT PREVENT MED & ENVIRONM HLTH BIOSTAT, IOWA CITY, IA 52242 USA
[3] UNIV IOWA, COLL MED, DEPT PATHOL, IOWA CITY, IA 52242 USA
关键词
ACUTE LEUKEMIA; CLASSIFICATION; FEATURES; THERAPY; PROGNOSIS; M0; UNDIFFERENTIATED ACUTE LEUKEMIA; PEROXIDASE-NEGATIVE;
D O I
10.1016/0145-2126(93)90002-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have studied 35 adult patients with morphologically undifferentiated peroxidase-negative acute leukemia that failed to meet the criteria for acute lymphoblastic leukemia and compared them to patients with FAB Ml-M7 seen by the same physicians. The diagnosis of minimally differentiated acute leukemia (MD-AL) was associated with a higher incidence of prior hematologic disease, lower WBC, fewer blood blasts, lower marrow cellularity and a tendency towards older age. Of all patients treated with AML since January 1983, those with MD-AL were less likely to get a complete remission than those with other subtypes (35 vs 64%, p = 0.03). Treatment failure was usually due to resistant disease. Analysis of outcome as a function of drugs used during induction therapy showed an advantage for regimens containing vincristine and prednisone. The leukemic blast cells of nine patients were immunophenotyped for myeloid, lymphoid and megakaryoblast/platelet antigens. Although there were too few for a full statistical analysis as was applied to the larger group of 35 patients with MD-AL, these patients had a lower bone marrow cellularity as compared to FAB M1-M7 and a low remission rate. Eight of these were found to have positive myeloid markers and met the criteria for FAB MO. We conclude that patients with MD-AL form a distinct group with characteristic presenting features and a low response rate. Outcome data suggest that vincristine and prednisone should be included in experimental induction programs.
引用
收藏
页码:199 / 208
页数:10
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