Drug resistance factors in acute myeloid leukemia:: a comparative analysis

被引:48
作者
Filipits, M
Stranzl, T
Pohl, G
Heinzl, H
Jäger, U
Geissler, K
Fonatsch, C
Haas, OA
Lechner, K
Pirker, R
机构
[1] Univ Vienna, Sch Med, Dept Internal Med 1, Div Oncol, A-1090 Vienna, Austria
[2] Univ Vienna, Sch Med, Dept Internal Med 1, Div Hematol, A-1090 Vienna, Austria
[3] Univ Vienna, Sch Med, Dept Med Comp Sci, A-1090 Vienna, Austria
[4] Univ Vienna, Sch Med, Dept Med Biol, A-1090 Vienna, Austria
[5] St Anna Childrens Hosp, Vienna, Austria
基金
奥地利科学基金会;
关键词
multidrug resistance; P-glycoprotein; MRP1; LRP; bcl-2; acute myeloid leukemia;
D O I
10.1038/sj.leu.2401634
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To compare the clinical relevance of drug resistance factors in de novo acute myeloid leukemia (AML), we determined their relationship to both response to induction chemotherapy and survival of the patients in univariate as well as multivariate analyses. The drug resistance factors immunocytochemically studied in 111 patients at the time of diagnosis included the lung resistance protein (LRP), P-glycoprotein (P-gp), multidrug resistance protein (MRP1) and bcl-2. In the univariate analyses, age (P = 0.005), karyotype (P = 0.03), LRP (P = 0.003), P-gp (P = 0.02) and bcl-2 (P = 0.03) predicted for response to induction chemotherapy, whereas MRP1 had no predictive value. Age (P = 0,05), karyotype (P = 0.05) and LRP (P = 0.03) retained their predictive value in the multivariate logistic regression analyses. With regard to overall survival, age (P = 0.008), karyotype (P = 0.006), LRP (P = 0.001) and P-gp (P = 0.01) were of prognostic value in the univariate Cox regression analyses but only age (P = 0.01), karyotype (P = 0.02) and LRP (P = 0.01) retained their prognostic significance in the multivariate analyses. A risk score based on the number of independent prognostic factors allowed division of patients into four groups with different outcome. In these groups, the complete remission rates were 93%, 75%, 47% and 33%, respectively, and median overall survival was 2.4, 1.2, 0.6 and 0.2 years, respectively. Thus, several drug resistance factors did predict outcome in the univariate analyses but LRP was the only drug resistance factor with independent predictive and prognostic significance. The proposed risk score might be useful for risk-adapted treatment in the future.
引用
收藏
页码:68 / 76
页数:9
相关论文
共 48 条
[1]   Treatment of refractory and relapsed acute myelogenous leukemia with combination chemotherapy plus the multidrug resistance modulator PSC833 (Valspodar) [J].
Advani, R ;
Saba, HI ;
Tallman, MS ;
Rowe, JM ;
Wiernik, PH ;
Ramek, J ;
Dugan, K ;
Lum, B ;
Villena, J ;
Davis, E ;
Paietta, E ;
Litchman, M ;
Sikic, BI ;
Greenberg, PL .
BLOOD, 1999, 93 (03) :787-795
[2]  
Beck WT, 1996, CANCER RES, V56, P3010
[3]  
Bloomfield CD, 1997, CANCER-AM CANCER SOC, V80, P2191
[4]   Overexpression of lung-resistance protein and increased P-glycoprotein function in acute myeloid leukaemia cells predict a poor response to chemotherapy and reduced patient survival [J].
Borg, AG ;
Burgess, R ;
Green, LM ;
Scheper, RJ ;
Yin, JAL .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (04) :1083-1091
[5]   Do P-glycoprotein and major vault protein (MVP/LRP) expression correlate with in vitro daunorubicin resistance in acute myeloid leukemia [J].
Broxterman, HJ ;
Sonneveld, P ;
Pieters, R ;
Lankelma, J ;
Eekman, CA ;
Loonen, AH ;
Schoester, M ;
Ossenkoppele, GJ ;
Löwenberg, B ;
Pinedo, HM ;
Schuurhuis, GJ .
LEUKEMIA, 1999, 13 (02) :258-265
[6]  
CAMPOS L, 1993, BLOOD, V81, P3091
[7]  
CAMPOS L, 1992, BLOOD, V79, P473
[8]   Simultaneous expression of p-glycoprotein and BCL-2 in acute myeloid leukemia blast cells [J].
Campos, L ;
Oriol, P ;
Sabido, O ;
Guyotat, D .
LEUKEMIA & LYMPHOMA, 1997, 27 (1-2) :119-125
[9]  
COX DR, 1972, J R STAT SOC B, V34, P187
[10]  
DelPoeta G, 1997, LEUKEMIA LYMPHOMA, V27, P257