Combined analysis of ZAP-70 and CD38 expression as a predictor of disease progression in B-cell chronic lymphocytic leukemia

被引:171
作者
Schroers, R
Griesinger, F
Trümper, L
Haase, D
Kulle, B
Klein-Hitpass, L
Sellmann, L
Dührsen, U
Dürig, J
机构
[1] Univ Goettingen, Dept Hematol & Oncol, D-37099 Gottingen, Germany
[2] Univ Goettingen, Dept Genet Epidemiol, Gottingen, Germany
[3] Univ Hosp Essen, Inst Cell Biol, Essen, Germany
[4] Univ Duisburg Essen, Univ Hosp Essen, Dept Hematol, D-45122 Essen, Germany
关键词
B-cell chronic lymphocytic leukemia (B-CLL); protein tyrosine kinase ZAP-70; CD38; antigen; IgV(H) status; genomic aberrations; cDNA microarray analysis;
D O I
10.1038/sj.leu.2403707
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prognostic predictions in B-cell chronic lymphocytic leukemia (B-CLL) at early clinical stage are based on biological disease parameters, such as ZAP-70 and CD38 protein levels, genomic aberrations as well as immunoglobulin variable heavy chain gene (IgV(H)) mutation status. In the current study, ZAP-70 and CD38 expressions were examined by flow cytometry in 252 patients with B-CLL. Cytoplasmic ZAP-70 expression in more than 20% (ZAP-70(+)) and surface CD38 expression on more than 30% (CD38(+)) of B-CLL cells were associated with an unfavorable clinical course. The levels of ZAP-70 and CD38 did not change over time in the majority of patients where sequential samples were available for analysis. Combined analysis of ZAP-70 and CD38 yielded discordant results in 73 patients (29.0%), whereas 120 patients (47.6%) were concordantly negative and 59 patients (23.4%) were concordantly positive for ZAP-70 and CD38 expression. Median treatment-free survival times in patients whose leukemic cells were ZAP-70(+)CD38(+) was 30 months as compared to 130 months in patients with a ZAP-70(-)CD38(-) status. In patients with discordant ZAP-70/CD38 results, the median treatment-free survival time was 43 months. Thus, ZAP-70 and CD38 expression analyses provided complementary prognostic information identifying three patient subgroups with good, intermediate and poor prognosis. Over-representation of high-risk genomic aberrations such as 17p deletion or 11q deletion and distribution of the IgVH mutation status in B-CLL discordant for ZAP-70/ CD38 pointed toward a distinct biologic background of the observed disease subgroups. This finding was also supported by microarray-based gene expression profiling in a subset of 35 patients. The expression of 37 genes differed significantly between the three groups defined by their expression of ZAP-70 and CD38, including genes that are involved in regulation of cell survival and chemotherapy resistance.
引用
收藏
页码:750 / 758
页数:9
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