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本文引用的文献

1
[Clinical effect of CCLG-ALL2008 regimen in treatment of children and adolescents aged >10 years with acute lymphoblastic leukemia].CCLG-ALL2008方案治疗10岁以上儿童及青少年急性淋巴细胞白血病的临床疗效
Zhongguo Dang Dai Er Ke Za Zhi. 2019 May;21(5):405-410. doi: 10.7499/j.issn.1008-8830.2019.05.001.
2
Prognostic Effect of CD20 Expression in Adult B-cell Acute Lymphoblastic Leukemia.CD20 表达对成人 B 细胞急性淋巴细胞白血病的预后影响。
Clin Lymphoma Myeloma Leuk. 2018 May;18(5):361-367. doi: 10.1016/j.clml.2018.02.013. Epub 2018 Feb 26.
3
CD20 expression sub-stratifies standard-risk patients with B cell precursor acute lymphoblastic leukemia.CD20表达可对B细胞前体急性淋巴细胞白血病的标准风险患者进行亚分层。
Oncotarget. 2017 Oct 31;8(62):105397-105406. doi: 10.18632/oncotarget.22207. eCollection 2017 Dec 1.
4
CD20 positivity and white blood cell count predict treatment outcomes in Philadelphia chromosome-negative acute lymphoblastic leukemia patients ineligible for pediatric-inspired chemotherapy.CD20阳性和白细胞计数可预测不符合儿童启发式化疗条件的费城染色体阴性急性淋巴细胞白血病患者的治疗结果。
Jpn J Clin Oncol. 2017 Nov 1;47(11):1047-1054. doi: 10.1093/jjco/hyx126.
5
Immunophenotypic markers in adult acute lymphoblastic leukemia: the prognostic significance of CD20 and TdT expression.成人急性淋巴细胞白血病的免疫表型标志物:CD20和末端脱氧核苷酸转移酶(TdT)表达的预后意义
Blood Res. 2015 Dec;50(4):227-34. doi: 10.5045/br.2015.50.4.227. Epub 2015 Dec 21.
6
[CD20 Expression in Adult Patients with B-lineage Acute Lymphoblastic Leukemia and Its Prognostic Significance].[成人B系急性淋巴细胞白血病患者CD20表达及其预后意义]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2015 Jun;23(3):619-22. doi: 10.7534/j.issn.1009-2137.2015.03.003.
7
[A clinical study of drug-related toxicities of CCLG-ALL 08 protocol for childhood acute lymphoblastic leukemia].CCLG-ALL 08方案治疗儿童急性淋巴细胞白血病药物相关毒性的临床研究
Zhongguo Dang Dai Er Ke Za Zhi. 2013 Sep;15(9):737-42.
8
TGF-β-induced apoptosis of B-cell lymphoma Ramos cells through reduction of MS4A1/CD20.TGF-β 通过降低 MS4A1/CD20 诱导 B 细胞淋巴瘤 Ramos 细胞凋亡。
Oncogene. 2013 Apr 18;32(16):2096-106. doi: 10.1038/onc.2012.219. Epub 2012 Jun 4.
9
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Hematology. 2012 Mar;17(2):66-70. doi: 10.1179/102453312X13221316477741.
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CD20 expression has no prognostic role in Philadelphia-negative B-precursor acute lymphoblastic leukemia: new insights from the molecular study of minimal residual disease.CD20 表达在费城染色体阴性 B 前体细胞急性淋巴细胞白血病中无预后作用:微小残留病分子研究的新见解。
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[CD20并非高白细胞计数儿童B系急性淋巴细胞白血病的不良预后因素]

[CD20 is not a poor prognostic factor for childhood B-lineage acute lymphoblastic leukemia with high white blood cell count].

作者信息

Zhang Lu-Yang, Chen Xiao-Juan, Wang Shu-Chun, Guo Ye, Yang Wen-Yu, Chen Yu-Mei, Zhang Li, Zou Yao, Zhu Xiao-Fan

机构信息

State Key Laboratory of Experimental Hematology, National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin 300020, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2020 Jul;22(7):728-733. doi: 10.7499/j.issn.1008-8830.2001095.

DOI:10.7499/j.issn.1008-8830.2001095
PMID:32669169
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7389610/
Abstract

OBJECTIVE

To study the significance of CD20 combined with white blood cell (WBC) count at diagnosis in the prognosis assessment in children with B-lineage acute lymphoblastic leukemia (ALL).

METHODS

A retrospective analysis was performed on the medical data of 821 B-ALL children who were treated with CCLG-ALL2008 regimen from April 2008 to April 2015. Their survival status was followed up.

RESULTS

Among the 821 children, 547 (66.6%) were negative, while 274 (33.4%) were positive for CD20 expression. Among 694 children with WBC<50×10/L (lower WBC count), the 5-year EFS rates were 65.9%±3.2% and 77.3%±2.0% for CD20 positive and negative patients respectively (P=0.001); the 5-year OS rates were 78.3%±2.9% and 87.5%±1.6% for CD20 positive and negative patients respectively (P=0.005); CD20 positive expression was an independent risk factor for EFS (HR=1.634, P=0.001) and OS (HR=1.761, P=0.005). Among 127 children with WBC>50×10/L (higher WBC count), the 5-year EFS rates was 64.3%±7.7% and 53.7%±5.5% for CD20 positive and negative patients respectively (P=0.135); the 5-year OS rate was 81.4%±6.4% and 58.6%±5.6% for CD20 positive and negative patients respectively (P=0.022); CD20 positive expression was an independent protective factor for OS (HR=0.367, P=0.016).

CONCLUSIONS

In children with B-ALL who are treated with CCLG-ALL2008 regimen, those with CD20 positive expression in lower WBC count at diagnosis have a poor prognosis; however, those with CD20 positive expression in higher WBC count at diagnosis have a better long-time survival.

摘要

目的

探讨CD20联合白细胞(WBC)计数在B系急性淋巴细胞白血病(ALL)患儿诊断时对预后评估的意义。

方法

回顾性分析2008年4月至2015年4月采用CCLG-ALL2008方案治疗的821例B-ALL患儿的临床资料,并对其生存状况进行随访。

结果

821例患儿中,CD20表达阴性者547例(66.6%),阳性者274例(33.4%)。在694例白细胞计数<50×10⁹/L(低白细胞计数)的患儿中,CD20阳性和阴性患儿的5年无事件生存率(EFS)分别为65.9%±3.2%和77.3%±2.0%(P=0.001);5年总生存率(OS)分别为78.3%±2.9%和87.5%±1.6%(P=0.005);CD20阳性表达是EFS(风险比[HR]=1.634,P=0.001)和OS(HR=1.761,P=0.005)的独立危险因素。在127例白细胞计数>50×10⁹/L(高白细胞计数)的患儿中,CD20阳性和阴性患儿的5年EFS分别为64.3%±7.7%和53.7%±5.5%(P=0.135);5年OS分别为81.4%±6.4%和58.6%±5.6%(P=0.022);CD20阳性表达是OS的独立保护因素(HR=0.367,P=0.016)。

结论

采用CCLG-ALL2008方案治疗的B-ALL患儿,诊断时白细胞计数低且CD20阳性表达者预后较差;而诊断时白细胞计数高且CD20阳性表达者长期生存较好。