儿童急性淋巴细胞白血病中嗜生态病毒整合位点1 (EVI1)的临床特征及预后意义

IF 1.2 4区 医学 Q4 HEMATOLOGY Pediatric Hematology and Oncology Pub Date : 2023-05-01 DOI:10.1080/08880018.2022.2117881
Ming Jia, Bo-Fei Hu, Jing-Ying Zhang, Li-Yao Xu, Yong-Min Tang
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引用次数: 0

摘要

与关于EVI1在髓系恶性肿瘤中的广泛知识相反,关于儿童ALL中EVI1转录物的数据很少。本研究旨在探讨EVI1在小儿ALL患者中的临床和生物学意义,并验证其预后意义。在这里,我们通过实时聚合酶链反应(PCR)检测了837例根据中国儿童白血病国家方案(NPCLC)-ALL-2008方案治疗的新诊断ALL儿童中EVI1表达的临床和生物学意义,旨在探讨其在儿科ALL患者中的预后意义。837例患者中有27例(3.2%)检测到EVI1表达。EVI1过表达(EVI1+)组与EVI1-组在强的松反应、完全缓解率和复发率方面均无统计学差异。此外,我们发现两组的无事件生存期(EFS)和总生存期(OS)没有显著差异,多变量分析也没有发现EVI1+是一个独立的预后因素。在亚组分析中,在标准风险(SR)、中风险(IR)和高风险(HR)组中,EVI1+和EVI1-患者的临床结局没有差异。在最小残留病(MRD)-4组中,与EVI1-患者相比,EVI1+患者的EFS和OS发生率显著降低。需要进一步的大规模和精心设计的前瞻性研究来证实未来的结果。
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Clinical features and prognostic implications of ecotropic viral integration site 1 (EVI1) in childhood acute lymphoblastic leukemia.

In contrast to the extensive knowledge on EVI1 in myeloid malignancies, few data are available on the EVI1 transcript in pediatric ALL. The purpose of this study was to examine the clinical and biological significance of EVI1 and validate its prognostic significance in pediatric patients with ALL. Here, we examined the clinical and biological significance of EVI1 expression, as measured by real-time polymerase chain reaction (PCR) in 837 children with newly diagnosed ALL treated on the National Protocol of Childhood Leukemia in China (NPCLC)-ALL-2008 protocol, and aimed to explore their prognostic significance in pediatric ALL patients. The EVI1 expression was detected in 27 of 837 (3.2%) patients. No statistically significant differences in prednisone response, complete remission (CR) rates and relapse rates were found between EVI1 overexpression (EVI1+) group and EVI1- group. Moreover, we found no significant difference in event-free survival (EFS) and overall survival (OS) between these two groups, also multivariate analysis did not identify EVI1+ as an independent prognostic factor. In the subgroup analysis, there was no difference in clinical outcome between EVI1+ and EVI1- patients in standard‑risk (SR), intermediate-risk (IR) and high-risk (HR) groups. In the minimal residual disease (MRD)<10-4 group, EVI1+ patients have significantly lower EFS and OS rates compared to EVI1- patients. Further large‑scale and well‑designed prospective studies are required to confirm the results in the future.

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来源期刊
CiteScore
2.60
自引率
5.90%
发文量
71
审稿时长
6-12 weeks
期刊介绍: PHO: Pediatric Hematology and Oncology covers all aspects of research and patient management within the area of blood disorders and malignant diseases of childhood. Our goal is to make PHO: Pediatric Hematology and Oncology the premier journal for the international community of clinicians and scientists who together aim to define optimal therapeutic strategies for children and young adults with cancer and blood disorders. The journal supports articles that address research in diverse clinical settings, exceptional case studies/series that add novel insights into pathogenesis and/or clinical care, and reviews highlighting discoveries and challenges emerging from consortia and conferences. Clinical studies as well as basic and translational research reports regarding cancer pathogenesis, genetics, molecular diagnostics, pharmacology, stem cells, molecular targeting, cellular and immune therapies and transplantation are of interest. Papers with a focus on supportive care, late effects and on related ethical, legal, psychological, social, cultural, or historical aspects of these fields are also appreciated. Reviews on important developments in the field are welcome. Articles from scientists and clinicians across the international community of Pediatric Hematology and Oncology are considered for publication. The journal is not dependent on or connected with any organization or society. All submissions undergo rigorous peer review prior to publication. Our Editorial Board includes experts in Pediatric Hematology and Oncology representing a wide range of academic and geographic diversity.
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