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罗马尼亚急性淋巴细胞白血病患儿:一项长达十年的单中心研究结果

Children With Acute Lymphoblastic Leukemia in Romania: Results From a Decade-Long Single-Center Study.

作者信息

Neaga Alexandra, Jimbu Laura, Mesaros Oana, Blag Cristina, Zdrenghea Mihnea

机构信息

Department of Pediatric Oncology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, ROU.

Department of Hematology, Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, ROU.

出版信息

Cureus. 2024 Sep 25;16(9):e70166. doi: 10.7759/cureus.70166. eCollection 2024 Sep.

DOI:10.7759/cureus.70166
PMID:39463583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11505573/
Abstract

BACKGROUND

Acute lymphoblastic leukemia (ALL) is the most prevalent cancer in children, with continuously improving survival rates. As few studies in Romania have analyzed ALL patients and disease characteristics or survival, we conducted a retrospective study on 158 patients diagnosed with ALL admitted to the Department of Pediatric Oncology and Hematology at the Emergency Hospital for Children, Cluj-Napoca, Romania, from January 2011 until April 2021. The most important objectives of the study are to establish full profiles of the patients and ALL, remission rates, relapses, and deaths, an epidemiology analysis to determine the incidence of ALL for comparison with the standard European population, and also to assess survival by the most important parameters, including minimal residual disease (MRD).

METHODS

This was a retrospective study that focused on patients with newly diagnosed ALL from January 2011 to April 2021 in the Department of Pediatric Hematology and Oncology of the Emergency Hospital for Children, Cluj-Napoca, Romania. The inclusion criteria were: patients with de novo ALL, patients who were younger than 18 years of age, and patients with signed informed consents. The exclusion criteria included patients who were older than 18 years of age; patients with relapsed ALL; and patients who did not have a signed informed consent. A total of 158 patients were included in the study, aged between 0 and 17 years. The information about patient characteristics and all variables was taken from the patients' files, where informed consent is mandatorily stored. Descriptive statistics were used to evaluate variables such as age, gender, leukocyte number, immunophenotype, prednisone response, risk group assessment, cytogenetics, relapse, and MRD. Kaplan-Meier curves were used to assess survival, for which patients were divided into two subcohorts: a 2011-2015 subcohort and a 2016-2020 subcohort. The statistical analyses used Prism version 10.2.3 (GraphPad Software, La Jolla, CA). For the analysis, we used Kaplan-Meier curves, the log-rank (Mantel-Cox) test, the log-rank test for trends, the Gehan-Breslow-Wilcoxon test, survival proportions, the chi-square test, and correlations.

RESULTS

A shift in risk groups was observed after the introduction of MRD testing in 2017, with more patients being stratified in the medium-risk group (MRG) and high-risk group (HRG). At the survival analyses between bone marrow (BM) aspiration and MRD on day 15, we discovered that patients with MRD>10% had much higher overall survival (OS) and event-free survival (EFS) compared to patients with >25% blasts in the BM; 24(11.4%) patients relapsed, of which, nine (3.8%) were very early relapses and 10 (4.1%) were late relapses. The five-year OS and EFS for patients with the T-cell immunophenotype of ALL and those with leukocyte counts >100,000/mm were identical to those at one year.

CONCLUSIONS

The OS of the 2016-2020 subcohort was higher than that of the 2011-2015 subcohort, and more patients were stratified into MRG and HRGs due to the implementation of MRD testing. Minimal residual disease testing helped to improve significantly the survival rates of patients with more than 10% residual disease. None of the patients with very early relapses entered complete remission (CR), but all late relapses achieved CR. All events experienced by patients with the T-cell immunophenotype, or leukocyte counts of >100,000/mm occurred in the first year after diagnosis.

摘要

背景

急性淋巴细胞白血病(ALL)是儿童中最常见的癌症,其生存率在不断提高。由于罗马尼亚很少有研究分析ALL患者、疾病特征或生存率,我们对2011年1月至2021年4月期间在罗马尼亚克卢日-纳波卡市儿童急救医院儿科肿瘤血液科收治的158例确诊为ALL的患者进行了一项回顾性研究。该研究的最重要目标是建立患者和ALL的完整档案、缓解率、复发率和死亡率,进行流行病学分析以确定ALL的发病率并与欧洲标准人群进行比较,同时通过包括微小残留病(MRD)在内的最重要参数评估生存率。

方法

这是一项回顾性研究,重点关注2011年1月至2021年4月期间罗马尼亚克卢日-纳波卡市儿童急救医院儿科血液肿瘤科新诊断为ALL的患者。纳入标准为:初发ALL患者、年龄小于18岁的患者以及签署知情同意书的患者。排除标准包括年龄大于18岁的患者;复发ALL患者;以及未签署知情同意书的患者。共有158例年龄在0至17岁之间的患者纳入研究。关于患者特征和所有变量的信息取自患者档案,其中强制存储了知情同意书。使用描述性统计来评估年龄、性别、白细胞计数、免疫表型、泼尼松反应、风险组评估、细胞遗传学、复发和MRD等变量。使用Kaplan-Meier曲线评估生存率,为此将患者分为两个亚组:2011 - 2015亚组和2016 - 2020亚组。统计分析使用Prism 10.2.3版本(GraphPad软件,加利福尼亚州拉霍亚)。分析中,我们使用了Kaplan-Meier曲线、对数秩(Mantel-Cox)检验、趋势对数秩检验、Gehan-Breslow-Wilcoxon检验、生存比例、卡方检验和相关性分析。

结果

2017年引入MRD检测后观察到风险组发生了变化,更多患者被分层到中风险组(MRG)和高风险组(HRG)。在第15天进行骨髓穿刺和MRD的生存分析中,我们发现MRD>10%的患者与骨髓中原始细胞>25%的患者相比,总生存率(OS)和无事件生存率(EFS)要高得多;24例(11.4%)患者复发,其中9例(3.8%)为早期复发,10例(4.1%)为晚期复发。ALL T细胞免疫表型且白细胞计数>100,000/mm³的患者的五年OS和EFS与一年时相同。

结论

2016 - 2020亚组的OS高于2011 - 2015亚组,并且由于实施了MRD检测,更多患者被分层到MRG和HRG。微小残留病检测有助于显著提高残留病超过10%的患者的生存率。所有早期复发的患者均未进入完全缓解(CR),但所有晚期复发的患者均实现了CR。ALL T细胞免疫表型或白细胞计数>100,000/mm³的患者经历的所有事件均发生在诊断后的第一年。

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