Ouyang Mei-Fei, Wang Dan, Liu Ying-Ting, Xu Lin-Yong, Zhao Ming-Yi, Yin Xiao-Cheng, Xie Min, Yang Liang-Chun, Yang Ming-Hua
Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China.
Zhongguo Dang Dai Er Ke Za Zhi. 2019 Apr;21(4):359-364. doi: 10.7499/j.issn.1008-8830.2019.04.011.
To study the association between S100A8 expression and prognosis in children with acute lymphoblastic leukemia (ALL).
The clinical data of 377 children with ALL who were treated with the CCLG-2008-ALL regimen were retrospectively reviewed. ELISA and PCR were used to measure serum protein levels and mRNA expression of S100A8. The Kaplan-Meier method was used for survival analysis and a Cox regression analysis was also performed.
The children were followed up for 56 months, and the overall survival rate of the 377 children was 89.1%. The prednisone good response group had significantly lower S100A8 protein and mRNA levels than the prednisone poor response group (P<0.01). In the children with standard or median risk, both S100A8 protein and mRNA levels were associated with event-free survival rate (P<0.05). There were significant differences in S100A8 protein and mRNA levels between the children with different risk stratifications (P<0.01). The children who experienced events had significantly higher S100A8 protein and mRNA levels than those who did not (P<0.01). The Kaplan-Meier survival analysis and the Cox regression model suggested that S100A8 overexpression was an independent risk factor for the prognosis of children with ALL.
High S100A8 expression may be associated with the poor prognosis of children with ALL and is promising as a new marker for individualized precise treatment of children with ALL.
研究S100A8表达与急性淋巴细胞白血病(ALL)患儿预后的关系。
回顾性分析377例采用CCLG - 2008 - ALL方案治疗的ALL患儿的临床资料。采用ELISA和PCR检测血清S100A8蛋白水平及mRNA表达。采用Kaplan - Meier法进行生存分析,并进行Cox回归分析。
对患儿随访56个月,377例患儿的总生存率为89.1%。泼尼松反应良好组的S100A8蛋白和mRNA水平显著低于泼尼松反应不良组(P<0.01)。在标准或中危患儿中,S100A8蛋白和mRNA水平均与无事件生存率相关(P<0.05)。不同危险分层患儿的S100A8蛋白和mRNA水平存在显著差异(P<0.01)。发生事件的患儿的S100A8蛋白和mRNA水平显著高于未发生事件的患儿(P<0.01)。Kaplan - Meier生存分析和Cox回归模型表明,S100A8过表达是ALL患儿预后的独立危险因素。
S100A高表达可能与ALL患儿预后不良有关,有望作为ALL患儿个体化精准治疗的新标志物。