CD69 is independently prognostic in chronic lymphocytic leukemia: a comprehensive clinical and biological profiling study

被引:28
作者
Del Poeta, Giovanni [1 ]
Del Principe, Maria Ilaria [1 ]
Zucchetto, Antonella [2 ]
Luciano, Fabrizio [1 ]
Buccisano, Francesco [1 ]
Rossi, Francesca Maria [2 ]
Bruno, Antonio [1 ]
Biagi, Annalisa [1 ]
Bulian, Pietro [2 ]
Maurillo, Luca [1 ]
Neri, Benedetta [1 ]
Bomben, Riccardo [2 ]
Simotti, Cristina [1 ]
Coletta, Angela Maria [1 ]
Dal Bo, Michele [2 ]
de Fabritiis, Paolo [1 ]
Venditti, Adriano [1 ]
Gattei, Valter [2 ]
Amadori, Sergio [1 ]
机构
[1] Univ Tor Vergata, Dept Hematol, I-00144 Rome, Italy
[2] Ctr Riferimento Oncol, Clin & Expt Oncohematol Res Unit, Aviano, PN, Italy
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2012年 / 97卷 / 02期
关键词
chronic lymphocytic leukemia; immunophenotyping; prognosis; ANTIGEN-DRIVEN SELECTION; GENE MUTATION STATUS; CD38; EXPRESSION; ZAP-70; GENOMIC ABERRATIONS; PROTEIN EXPRESSION; CELLS; SURVIVAL; RECEPTOR; ACTIVATION;
D O I
10.3324/haematol.2011.052829
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background CD69 is expressed in several hemopoietic cells and is an early activation marker in chronic lymphocytic leukemia. Chronic lymphocytic leukemia is a clinically heterogeneous disease which needs novel prognostic parameters which can be easily and efficiently managed. Design and Methods We investigated CD69 by flow cytometry in a series of 417 patients affected by chronic lymphocytic leukemia and compared this to other biological and clinical prognosticators. Results CD69 was associated with Rai stages (P=0.00002), beta(2)-microglobulin (P=0.0005) and soluble CD23 (P<0.0001). CD69 and ZAP-70 (P=0.018) or CD38 (P=0.00015) or immunoglobulin variable heavy chain gene mutations (P=0.0005) were also significantly correlated. Clinically, CD69 positive chronic lymphocytic leukemias received chemotherapy more frequently (74%; P<0.0001), and presented a shorter duration of response after fludarabine plus rituximab (P=0.010) as well as shorter progression free survival and overall survival (P<0.0001). CD69 demonstrated true additive prognostic properties, since the CD69(+) plus ZAP-70(+) or CD38(+) or immunoglobulin variable heavy chain gene unmutated patients had the worst progression free survival and overall survival (P<0.0001). Interestingly, low CD69 expression was necessary to correctly prognosticate the longer progression free survival of patients with a low tumor burden of beta(2)-microglobulin (P=0.002), of soluble CD23 (P=0.020), or of Rai stages 0-I (P=0.005). CD69 was confirmed to be an independent prognostic factor in multivariate analysis of progression free survival (P=0.017) and overall survival (P=0.039). Conclusions Our data indicate that CD69 is significantly correlated with poor clinical and biological prognostic factors and is confirmed to be an independent disease prognosticator. This supports its introduction in a routine laboratory assessment and, possibly, in a prognostic scoring system for chronic lymphocytic leukemia, after an adequate standardization process.
引用
收藏
页码:279 / 287
页数:9
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