Prognostic significance of recurrent additional chromosomal abnormalities in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia

被引:10
作者
Seol, Chang Ahn [1 ,2 ]
Cho, Young-Uk [1 ,2 ]
Jang, Seongsoo [1 ,2 ]
Park, Chan-Jeoung [1 ,2 ]
Lee, Jung-Hee [2 ,3 ]
Lee, Je-Hwan [2 ,3 ]
Lee, Kyoo Hyung [2 ,3 ]
Seo, Eul-Ju [1 ,2 ]
机构
[1] Univ Ulsan, Coll Med, Dept Lab Med, Seoul, South Korea
[2] Asan Med Ctr, Seoul, South Korea
[3] Univ Ulsan, Coll Med, Dept Internal Med, Seoul, South Korea
关键词
Acute lymphoblastic leukemia; Philadelphia chromosome-positive; additional hromosomal abnormality; prognosis; CHILDRENS ONCOLOGY GROUP; CYTOGENETIC ABNORMALITIES; IMPACT; CHEMOTHERAPY;
D O I
10.1016/j.cancergen.2017.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In Philadelphia (Ph) chromosome-positive acute lymphoblastic leukemia (ALL), additional chromosomal abnormalities (ACAs) are frequently observed. We investigated the cytogenetic characteristics and prognostic significance of ACAs in Ph-positive ALL. We reviewed the clinical data and bone marrow cytogenetic findings of 122 adult Ph-positive ALL patients. The ACAs were examined for partial or whole chromosomal gains or losses, and structural aberrations. The overall survival (OS) and disease-free survival (DFS) of patients who received hematopoietic cell transplantation were compared between the isolated Ph group and ACA group. ACAs were present in 73.0% of all patients. The recurrent ACAs were extra Ph (24.7%), 9/9p loss (20.2%), and 7/7p loss (19.1%). Complex karyotype was found in 28.1% of patients in the ACA group. Younger patients (19-30 years) in the ACA group showed the highest frequency of extra Ph (54%) compared to other age groups. The OS in the ACA group was significantly shorter than in the isolated Ph group. The presence of an extra Ph chromosome or 9/9p loss was significantly associated with shorter OS and DFS, whereas 7/7p loss and complex karyotype were not associated with poorer prognosis. We suggest that subclassification of ACAs could be applied to prognostic investigation of Ph-positive ALL.
引用
收藏
页码:29 / 36
页数:8
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