Genetic, Cytogenetic and Hematological Features in Newly Diagnosed Acute Lymphoid Leukemia Patients under Eighteen Years Age Rreferred to Ali Asghar Hospital of Tehran, Iran, from 2013 to 2023.

Nafiseh Mortazavi, Aziz Eghbali, Omid Kiani Ghalesardi, Reza Afrisham, Reza Asadpouri, Zahra Salehi, Soudabeh Hosseini, Elahe Razmara Lak
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Abstract

Introduction: Acute lymphoblastic leukemia (ALL), a hematopoietic cancer of T or B lymphoblasts, is the most prevalent cancer in children. Ongoing research aims to better understand the factors contributing to ALL and create more successful treatment options. Therefore, the current study presented cytogenetic, genetic, and hematologic features from 318 ALL patients under eighteen years of age who were referred to Ali Asghar Hospital of Tehran, Iran, from 2013 to 2023.

Methods: This study was designed as a retrospective cross-sectional analysis, focusing on 318 children in Tehran, Iran, who had been newly diagnosed with ALL. All data were extracted from the patient case files that included additional information, such as clinical data, and demographic information. The Flow cytometry technique was employed to perform immunophenotyping for various markers. Moreover, the standardized protocol was carried out for conventional cytogenetic analysis.

Results: Out of 318, 179 (56.3%) and 139 (43.7%) were males and females, respectively. The most common subtype of ALL was Common B Cell ALL, accounting for 182 cases (57.23%), followed by Pre B cell ALL with 74 cases (23.27%) and T cell ALL with 27 cases (8.49%). Out of 222 patients, 17 (7.7%) had genetic abnormalities, with the highest incidence of abnormalities being associated with Runx 1 (four cases). Additionally, out of 228 patients, 143 (62.7%) were identified as having cytogenetic abnormalities, with the most prevalent abnormalities being hyperdiploidy (54 cases) and t (12;21) (28 cases).

Conclusion: Our findings showed that some cytogenetic abnormalities, such as t (9;22) and hyperdiploidy, were consistent with previous studies. These results offer valuable foundational insights that can help direct future research on ALL patients and inform potential treatment strategies.

2013年至2023年伊朗德黑兰Ali Asghar医院新诊断的18岁以下急性淋巴性白血病患者的遗传、细胞遗传学和血液学特征
简介:急性淋巴细胞白血病(ALL)是一种T淋巴细胞或B淋巴细胞造血肿瘤,是儿童中最常见的癌症。正在进行的研究旨在更好地了解导致ALL的因素,并创造更成功的治疗方案。因此,目前的研究报告了2013年至2023年在伊朗德黑兰Ali Asghar医院转诊的318名18岁以下ALL患者的细胞遗传学、遗传学和血液学特征。方法:本研究采用回顾性横断面分析,以伊朗德黑兰318例新诊断为ALL的儿童为研究对象。所有数据均从患者病例文件中提取,其中包括附加信息,如临床数据和人口统计信息。采用流式细胞术技术对各种标记物进行免疫分型。此外,标准化方案进行常规细胞遗传学分析。结果:318例患者中,男179例(56.3%),女139例(43.7%)。ALL最常见亚型为普通B细胞ALL,占182例(57.23%),其次为Pre B细胞ALL 74例(23.27%),T细胞ALL 27例(8.49%)。222例患者中,17例(7.7%)存在遗传异常,其中与runx1相关的异常发生率最高(4例)。此外,在228例患者中,143例(62.7%)被确定为细胞遗传学异常,最常见的异常是高二倍体(54例)和t(12例;21例)(28例)。结论:我们的研究结果表明,一些细胞遗传学异常,如t(9;22)和高二倍体,与以往的研究一致。这些结果提供了有价值的基础见解,可以帮助指导未来对ALL患者的研究,并为潜在的治疗策略提供信息。
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