A scoring system based on the expression of six surface molecules allows the identification of three prognostic risk groups in B-cell chronic lymphocytic leukemia

被引:42
作者
Zucchetto, A
Bomben, R
Dal Bo, M
Sonego, P
Nanni, P
Rupolo, M
Bulian, P
Dal Maso, L
Del Poeta, G
Del Principe, MI
Degan, M
Gattei, V
机构
[1] IRCCS, Ctr Riferimento Oncol, Clin & Expt Hematol Res Unit, Aviano, PN, Italy
[2] IRCCS, Ctr Riferimento Oncol, Epidemiol & Biostat Unit, Aviano, PN, Italy
[3] Univ Roma Tor Vergata, Hematol Sect, Rome, Italy
关键词
D O I
10.1002/jcp.20570
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We have previously identified 12 surface antigens whose differential expression represented the signature of B-cell chronic lymphocytic leukemia (B-CLL) Subsets with different prognosis. In the present study, expression data for these antigens, as determined in 137 B-CLL cases, all with survivals, were utilized to devise a comprehensive immunophenotypic scoring system of prognostic relevance for B-CLL patients. In particular, univariate z score was employed to identify the markers with greater prognostic impact, while maximally selected log-rank statistics were chosen to define the optimal cut-off points capable to split patients into two groups with different survivals. A weighted immunophenotypic scoring system was developed by integrating results from these analyses. Six antigens were selected: three positive prognosticators (CD62L, CID54, CD496 and three negative prognosticators (CD49d, CD38, CD79b), with cut-off values ranging from 30% to 50% of positive cells. By weighing the expression of each marker according to its statistical power, a complete scoring system, with point values comprised between 0 (complete absence of phenotypic conditions associated with good prognosis) and 9 (all the phenotypic conditions associated with good prognosis fulfilled), allowed to split the whole set of B-CLL patients, into three distinctive prognostic groups (P= 4.78 x 10(-11)) with high- (score-0-3), intermediate- (score4-6), and low-(score 7-9) risk of death. The three risk groups showed different distribution of cases as for Rai's stages, IgV(H) mutations, and ZAP-70 expression. The proposed immunophenotypic scoring system may be an additional useful tool in routine diagnostic/prognostic procedures for B-CLL. J. Cell. Physiol. 207: 354-363, 2006. (c) 2005 Wiley-Liss, Inc.
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页码:354 / 363
页数:10
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