Multivariate analysis of prognostic factors in patients with refractory and relapsed acute myeloid leukemia undergoing sequential high-dose cytosine arabinoside and mitoxantrone (S-HAM) salvage therapy:: relevance of cytogenetic abnormalities

被引:66
作者
Kern, W [1 ]
Schoch, C
Haferlach, T
Braess, J
Unterhalt, M
Wörmann, B
Büchner, T
Hiddemann, W
机构
[1] Univ Munich, Dept Med 3, Hosp Grosshadern, D-81366 Munich, Germany
[2] City Hosp, Dept Med, Braunschweig, Germany
[3] Univ Munster, Dept Med A, D-4400 Munster, Germany
关键词
AML; cytogenetics; prognostic factors; high-dose AraC; mitoxantrone;
D O I
10.1038/sj.leu.2401668
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To improve the basis for the stratification of patients with refractory and relapsed acute myeloid leukemia (AML) univariate and multivariate analyses of prognostic factors were performed in 254 patients (median age 50 years, range 18-74) undergoing S-HAM salvage chemotherapy during two consecutive prospective trials of the German AML Cooperative Group. In a multivariate analysis, duration of the first complete remission (CR) was the only factor associated with time to treatment failure (P = 0.0223). Disease-free survival was influenced by a short duration of the first CR of less than 6 months (P = 0.0001), WBC (P = 0.0018), blast count (P = 0.0037), and neutrophil count (P = 0.0119). The achievement of CR was related to the hemoglobin level only (P = 0.0457), the early death rate was related to age only (P = 0.0109), and survival was related to the bilirubin level only (P = 0.0166). In the subgroup of 104 patients in whom additional karyotype analyses were performed prior to first-line therapy unfavorable chromosome abnormalities were associated with a lower CR rate (univariate analysis, P = 0.0342; CR 24% vs 53%) and were the only factor related to survival. These analyses warrant the further evaluation of the impact of cytogenetic abnormalities on the outcome of patients with advanced AML in order to improve the characterization according to duration of first CR and to WBC of distinct subgroups of patients with differing prognoses as a basis for stratification in future trials.
引用
收藏
页码:226 / 231
页数:6
相关论文
共 52 条
[1]   TIMED SEQUENTIAL CHEMOTHERAPY FOR PREVIOUSLY TREATED PATIENTS WITH ACUTE MYELOID-LEUKEMIA - LONG-TERM FOLLOW-UP OF THE ETOPOSIDE, MITOXANTRONE, AND CYTARABINE-86 TRIAL [J].
ARCHIMBAUD, E ;
THOMAS, X ;
LEBLOND, V ;
MICHALLET, M ;
FENAUX, P ;
CORDONNIER, C ;
DREYFUS, F ;
TROUSSARD, X ;
JAUBERT, J ;
TRAVADE, P ;
TRONCY, J ;
ASSOULINE, D ;
FIERE, D .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (01) :11-18
[2]   Timed sequential chemotherapy for advanced acute myeloid leukemia [J].
Archimbaud, E ;
Leblond, V ;
Fenaux, P ;
Dombret, H ;
Cordonnier, C ;
Dreyfus, F ;
ConyMakhoul, P ;
Tilly, H ;
Troussard, X ;
Auzanneau, G ;
Thomas, X ;
Ffrench, M ;
Marie, JP .
HEMATOLOGY AND CELL THERAPY, 1996, 38 (02) :161-167
[3]   PROPOSED REVISED CRITERIA FOR THE CLASSIFICATION OF ACUTE MYELOID-LEUKEMIA - A REPORT OF THE FRENCH-AMERICAN-BRITISH COOPERATIVE GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :620-625
[4]  
Bloomfield CD, 1997, CANCER-AM CANCER SOC, V80, P2191
[5]  
Bloomfield CD, 1998, CANCER RES, V58, P4173
[6]  
BUCHNER T, 1985, J CLIN ONCOL, V3, P1583
[7]  
BUCHNER T, 1992, LEUKEMIA, V6, P68
[8]  
BUCHNER T, 1997, BLOOD, V90, pA504
[9]  
Byrd JC, 1998, CLIN CANCER RES, V4, P1235
[10]  
CARELLA AM, 1993, LEUKEMIA, V7, P196