Clinical Significance of CRLF2 High Expression in Bone Marrow Mononuclear Cells from Children with Acute Lymphoblastic Leukemia.
10.19746/j.cnki.issn.1009-2137.2019.04.011
- Author:
Wen-Yong KUANG
1
;
Wan-Li LI
1
;
Min-Cui ZHENG
1
;
Hai-Xia YANG
1
;
Ben-Shan ZHANG
1
;
Pan WU
1
;
Shan HE
1
;
Na SONG
1
;
Rui-Juan LI
2
Author Information
1. Department of Hematology, Hunan Provincial Children's Hospital, Changsha 410007, Hunan Province, China.
2. Department of Hematology, The Second Xiangya Hospital of Central South University, Changsha 410011, Hunan Province, China,E-mail: Kathy5460@sina.com.
- Publication Type:Journal Article
- MeSH:
Bone Marrow;
Child;
Humans;
Precursor Cell Lymphoblastic Leukemia-Lymphoma;
Prognosis;
Receptors, Cytokine;
metabolism;
Recurrence;
Risk Factors
- From:
Journal of Experimental Hematology
2019;27(4):1058-1063
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To detect the expression of CRLF2 in bone marrow mononuclear cells from children with newly diagnosed acute lymphoblastic leukemia(ALL) and to explore its clinical significance in pediatric ALL.
METHODS:A total of 218 children with newly diagnosed ALL who achieveal the complete remission and had the complete follow-up information were selected, and the expression level of CRLF2 in bone marrow mononuclear cells of these children was detected by real-time fluorescent quantitative PCR, and the significance of CRLF2 expression level in clinical prognosis of ALL children was analyzed by using statistical method.
RESULTS:28 cases in 218 children with complete data showed high expression of CRLF2. The cumulative recurrence rate in the CRLF2 high expression group was significantly higher than that in the low expression group (53.6% vs 12.6%) (P＜0.01). The predicted 5-year recurrence-free survival rate (RFS) of ALL children with CRLF2 high expression was significantly higher than that of low expression group (P＜0.01). There was no significant difference in the predicted 5-year RFS between ALL children with CRLF2 low and high expression in the standard-risk(SR) group (P＞0.05). The predicted 5-year RFS of ALL children with CRLF2 low expression was higher than that of ALL children with CRLF2 high expression in the intermediate-risk (IR) and high-risk (HR) groups. (P＜0.05). Cox analysis showed that CRLF2 high expression is an independent risk factor for the relapse of children with ALL.
CONCLUSION:The recurrence rate of pediatric ALL with CRLF2 high expression is high, and CRLF2 high expression is an important prognostic factor for high risk of relapse in ALL children with IR and HR. It is necessary to use CRLF2 expression as an indicator of risk stratification in pediatric ALL.
