Current trends in the diagnosis and treatment of acute tumor lysis syndrome in children: a review

N. Matinyan, T. Valiev, L. Martynov, V. Akimov, E. A. Kovaleva, Yuri V. Buidenok
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Abstract

INTRODUCTION: Acute tumor lysis syndrome (ATLS) complicates the treatment of highly aggressive leukemia, lymphomas in children and is accompanied by a fatal outcome in 21.4 % of patients. The basis of ATLS is the decay of tumor cells, in which the volume of decay products exceeds the excretory capabilities of the kidneys. The ATLS risk group includes patients with acute lymphoblastic leukemia accompanied by hyperleukocytosis (above 100×109/L) and non-Hodgkin's lymphomas with a large tumor mass (III–IV stages of the disease). To date, the volume of thematic publications in the aggregator of the PubMed medical database is not so large: over the past 10 years, there have been 12 articles, which makes the task of systematizing previously accumulated and recently received information even more relevant for the practitioner. OBJECTIVE: Generalization of the modern scientific base for the diagnosis and treatment of ATLS in children. MATERIALS AND METHODS: To highlight the modern scientific base concerning the diagnosis and treatment of ATLS in children with oncohematological diseases, a search was conducted in PubMed, Research Gate, Web of Science Core Collection and Google Scholar systems for the period from 2000 to August 2022. RESULTS: In total, 94 articles were found, including 1 systematic review with meta-analysis and 16 review articles that meet the requirements. CONCLUSIONS: Conservative ATLS prophylaxis is effective in 93.4–93.6 % of patients. However, in 8.8–21.4 % of patients, ATLS acquires a rapid character, accompanied by the lack of the ability to conservatively correct the indicators of potassium, phosphorus, uric acid. Additional study of the pathogenetic mechanisms of the complication, identification of key targets of drug therapy and a multidisciplinary approach in the treatment of an extremely prognostically unfavorable group of oncohematological patients with advanced stages of the tumor process are possible components of further improving the effectiveness of ATLS therapy.
儿童急性肿瘤溶解综合征的诊断和治疗现状综述
简介:急性肿瘤溶解综合征(ATLS)使儿童高度侵袭性白血病、淋巴瘤的治疗复杂化,并伴有21.4%患者的致命结局。ATLS的基础是肿瘤细胞的衰变,其中衰变产物的体积超过了肾脏的排泄能力。ATLS危险组包括急性淋巴细胞白血病伴白细胞增多症(100×109/L以上)和大肿瘤块的非霍奇金淋巴瘤(疾病的III-IV期)患者。迄今为止,PubMed医学数据库聚合器中专题出版物的数量并不大:在过去的10年里,有12篇文章,这使得对以前积累和最近收到的信息进行系统化的任务对从业者来说更加相关。目的:总结儿童ATLS诊断和治疗的现代科学基础。材料与方法:为了突出血液肿瘤疾病儿童ATLS诊断与治疗的现代科学基础,检索PubMed、Research Gate、Web of Science Core Collection和Google Scholar系统,检索时间为2000年至2022年8月。结果:共检索到94篇文献,其中1篇系统综述进行meta分析,16篇综述符合要求。结论:保守性ATLS预防对93.4 - 93.6%的患者有效。然而,在8.8 - 21.4%的患者中,ATLS获得了快速的特征,并伴有缺乏保守校正钾、磷、尿酸指标的能力。进一步研究并发症的发病机制,确定药物治疗的关键靶点,以及采用多学科方法治疗预后极为不利的晚期肿瘤血液病患者,可能是进一步提高ATLS治疗有效性的组成部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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