Prognostic Effect of Complex Karyotype, Monosomal Karyotype, and Chromosome 17 Abnormalities in B-Cell Acute Lymphoblastic Leukemia

被引:4
|
作者
Khoral, Priya [1 ,2 ]
Atenafu, Eshetu G. [3 ]
Craddock, Kenneth J. [1 ,2 ]
Schimmer, Aaron [4 ]
Chang, Hong [1 ,2 ]
机构
[1] Univ Hlth Network, Dept Lab Hematol & Pathol, Toronto, ON M5G 2C4, Canada
[2] Univ Hlth Network, Dept Lab Med & Pathobiol, Toronto, ON, Canada
[3] Univ Hlth Network, Dept Biostat, Toronto, ON, Canada
[4] Univ Hlth Network, Dept Hematol & Med Oncol, Toronto, ON, Canada
关键词
Cytogenetic risk analysis; p53; Oncogenes; Multivariate analysis; Risk groups; ACUTE MYELOID-LEUKEMIA; DE-NOVO; TP53; MUTATIONS; ADULT PATIENTS; IMPACT; CYTOGENETICS; THERAPY; RELAPSE; CANCER; AML;
D O I
10.1016/j.clml.2017.02.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The effect of monosomal karyotype (MK), complex karyotype (CK) and chromosome 17 abnormalities on prognosis in B-cell acute lymphoid leukemia (B-ALL) has not yet been established. We conducted a retrospective analysis of prognostic factors on 237 adult patients with B-ALL treated at our institution. Our results showed that MK and CK do not play a predictive role in patients with B-ALL, but further study is required to determine whether specific changes on chromosome 17 might have prognostic value. Background: The effect of monosomal karyotype (MK), complex karyotype (CK), and chromosome 17 abnormalities (abnl 17) on prognosis in B-cell acute lymphoid leukemia (B-ALL) has not yet been established. Patients and Methods: We conducted a retrospective analysis of prognostic factors on 237 adult patients with B-ALL treated at our institution. Results: Older age (older than 60 years), higher white blood cell count (> 30), and abnl 17 were associated with shorter overall survival in univariate analysis, but multivariable analysis only identified older age as an independent poor prognostic actor. There was a significant correlation between abnl 17 and older age. Conclusion: In contrast to the patients with acute myeloid leukemia, our results show that MK and CK do not play a predictive role in patients with B-ALL, but further study is required to determine whether specific changes on chromosome 17 might have prognostic value when investigated separately.
引用
收藏
页码:215 / 219
页数:5
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