Long-term survival after induction therapy with idarubicin and cytosine arabinoside for de novo acute myeloid leukemia

被引:31
|
作者
Flasshove, M
Meusers, P
Schütte, J
Noppeney, R
Beelen, DW
Sohrab, S
Roggenbuck, U
Kemmeries, G
Brittinger, G
Seeber, S
Scheulen, ME
机构
[1] Univ Essen Gesamthsch, Sch Med, W German Canc Ctr,Inst Med Informat Biometry & Ep, Dept Internal Med Canc Res, D-45122 Essen, Germany
[2] Univ Essen Gesamthsch, Sch Med, W German Canc Ctr,Dept Hematol, Inst Med Informat Biometry & Epidemiol, D-45122 Essen, Germany
[3] Univ Essen Gesamthsch, Sch Med, W German Canc Ctr,Dept Bone Marrow Transplantat, Inst Med Informat Biometry & Epidemiol, D-45122 Essen, Germany
关键词
acute myeloid leukemia; cytosine arabinoside; idarubicin; induction therapy; karyotype;
D O I
10.1007/s002770000193
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We treated 153 patients with de novo acute myeloid leukemia (AML) with two induction courses of conventional-dose cytosine arabinoside (ara-C) and idarubicin (AIDA) followed by either a third course of AIDA, high-dose ara-C or bone-marrow transplantation. The complete remission (CR) rate for all patients was 63.4%, with a higher CR rate for patients with a normal (versus unfavorable) karyotype (73.2% vs 52.5%; P=0.038). The probability of overall survival (OS) was 30.7% after 5 years (26.3% after 7 years). Improved OS at 5 years could be observed for patients up to 50 years old versus patients older than 50 years of age (37.6% vs 19.9%; P=0.001) and patients with a normal (versus unfavorable) karyotype (42.9% vs 14.1%; P=0.0016). Disease-free survival (DFS) after 5 years was 33.2% for all 97 CR patients and was significantly better for patients with a normal (versus unfavorable) karyotype (44.3% vs 12.3%; P=0.003). Multivariate analysis revealed that the age for OS (P<0.02) and the karyotype for both OS (P<0.03) and DFS (P< 0.05) were independent prognostic factors. In conclusion, AIDA is an effective and well-tolerated induction regimen (even in elderly patients) with a 5-year survival of more than 30% when combined with ara-C-containing postremission therapy. The karyotype is the most powerful prognostic factor for predicting the outcome of patients treated with this protocol.
引用
收藏
页码:533 / 542
页数:10
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