Acute myeloid leukaemia MO:: haematological, immunophenotypic and cytogenetic characteristics and their prognostic significance:: an analysis in 241 patients

被引:52
作者
Béné, MC
Bernier, M
Casasnovas, RO
Castoldi, G
Doekharan, D
van der Holt, B
Knapp, W
Lemez, P
Ludwig, WD
Matutes, E
Orfao, A
Schoch, C
Sperling, C
van't Veer, MB
机构
[1] Univ Rotterdam Hosp, Dr Daniel den Hoed Canc Ctr, Dept Haematol, NL-3075 EA Rotterdam, Netherlands
[2] Fac Med, GEIL Lab Immunol, Nancy, France
[3] Inst Jules Bordet, B-1000 Brussels, Belgium
[4] Serv Hematol, Dijon, France
[5] Univ Ferrara, Inst Haematol, I-44100 Ferrara, Italy
[6] Univ Rotterdam Hosp, Dr Daniel den Hoed Canc Ctr, Dept Trials & Stat, NL-3075 EA Rotterdam, Netherlands
[7] Univ Vienna, Inst Immunol, A-1010 Vienna, Austria
[8] Hosp Jihlava, Dept Haematol & Blood Transfus, Jihlava, Czech Republic
[9] Humboldt Univ, Charite, Dept Haematol Oncol & Tumour Immunol, Robert Rossle Clin, Berlin, Germany
[10] Royal Marsden Hosp, Acad Dept Haematol & Cytogenet, London SW3 6JJ, England
[11] Univ Salamanca, Serv Citometria, E-37008 Salamanca, Spain
[12] Univ Munich, Dept Internal Med 3, D-80539 Munich, Germany
关键词
AML MO; clinical characteristics; immunophenotype; cytogenetics;
D O I
10.1046/j.1365-2141.2001.02801.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Haematological, immunophenotypic and cytogenetic characteristics were analysed in 241 patients with acute myeloid leukaemia (AML) M0, including 58 children. Children < 3 years and adults between 60 and 70 years of age were most frequently affected, Immunophenotyping showed a heterogeneous phenotype. Anti-myeloperoxidase was positive in about half of the patients. Cytogenetic data were available from 129 (54%) patients. A normal karyotype was found in only 24%. Most of the abnormalities were unbalanced and the chromosomes 5, 7, 8 and 11 were the most frequently affected, Survival data were available from 152 treated patients (63%), The median overall survival for all patients was 10 months, 20 months for children (n = 36), 10 months for the young adult group (n = 50) and 7 months for the elderly patients (n = 66) (P = 0.09). Karyotype was not a prognostic factor influencing survival. AML M0 shows the immunological characteristics of early progenitor cells, but the expression of the different markers and cytogenetic abnormalities is heterogeneous. The prognosis is poor compared with other de novo AML and similar to that of AML with multilineage dysplasia or AML following myelodysplastic syndromes.
引用
收藏
页码:737 / 745
页数:9
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