Prognostic significance of CD20 expression in adults with de novo precursor B-lineage acute lymphoblastic leukemia

被引:151
作者
Thomas, Deborah A. [1 ]
O'Brien, Susan [1 ]
Jorgensen, Jeffrey L. [2 ]
Cortes, Jorge [1 ]
Faderl, Stefan [1 ]
Garcia-Manero, Guillermo [1 ]
Verstovsek, Srdan [1 ]
Koller, Charles [1 ]
Pierce, Sherry [1 ]
Huh, Yang [2 ]
Wierda, William [1 ]
Keating, Michael J. [1 ]
Kantarjian, Hagop M. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
ACUTE LYMPHOCYTIC-LEUKEMIA; HYPER-CVAD; RITUXIMAB; CELL; LYMPHOMA; REGIMEN; THERAPY; CHEMOIMMUNOTHERAPY; CHEMOTHERAPY; RESISTANCE;
D O I
10.1182/blood-2008-04-151860
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immunophenotypic classification of acute lymphoblastic leukemia (ALL) has well-recognized prognostic implications. The significance of CD20 expression has been evaluated in childhood precursor B-lineage ALL with conflicting results. We retrospectively analyzed the influence of CD20 expression on outcome in 253 adults with de novo precursor B-lineage ALL treated with either conventional (VAD/CVAD) or intensive (hyper-CVAD) frontline chemotherapy regimens in the pre-rituximab era. Overall, CD20 positivity of at least 20% was associated with lower 3-year rates of complete remission duration (CRD; 20% vs 55%, P < .001) and overall survival (OS; 27% vs 40%, p = .03). In the CD20 negative subset, the 3-year rates for CRD (58% vs 42%, p = .04) and OS (60% vs 28%, P < .001) were superior for hyper-CVAD compared with VAD/CVAD; rates were particularly favorable for the CD20 negative younger age group (68% and 85%, respectively). In contrast, 3-year CRD and OS rates were uniformly poor for the CD20-positive group regardless of therapy (27% or less). Multivariate analysis for event-free survival identified older age, leukocyte count higher than 30 x 10(9)/L, presence of Philadelphia chromosome, high systemic risk classification, and CD20 positivity as independent predictors of worse outcome. In conclusion, CD20 expression in de novo adult precursor B-lineage ALL appears to be associated with a poor prognosis. Incorporation of monoclonal antibodies directed against CD20 into frontline chemotherapy regimens warrants investigation. (Blood. 2009; 113: 6330-6337)
引用
收藏
页码:6330 / 6337
页数:8
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