儿童急性淋巴细胞白血病的细胞遗传学和基因组学

IF 2.2 4区 医学 Q3 HEMATOLOGY
Željko Antić , Jana Lentes , Anke K. Bergmann
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引用次数: 0

摘要

在过去的五十年里,儿童急性淋巴细胞白血病(ALL)的诊断、治疗和管理有了显著改善。通过我们对ALL的遗传和生物学背景的理解,这些进展成为可能,从而引入了风险适应治疗和新的治疗靶点,例如BCR:ABL1阳性ALL的酪氨酸激酶抑制剂。ALL分类的进一步进展,新的遗传生物标志物和治疗靶点的发现,以及将靶向和免疫疗法引入一线治疗方案,可能会改善儿童ALL的管理和结果。在这篇综述中,我们描述了ALL儿童(细胞)基因诊断和管理的最新进展,并概述了ALL基因分类的最重要进展。此外,我们还讨论了包括人工智能在内的新技术发展带来的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytogenetics and genomics in pediatric acute lymphoblastic leukaemia

The last five decades have witnessed significant improvement in diagnostics, treatment and management of children with acute lymphoblastic leukaemia (ALL). These advancements have become possible through progress in our understanding of the genetic and biological background of ALL, resulting in the introduction of risk-adapted treatment and novel therapeutic targets, e.g., tyrosine kinase inhibitors for BCR::ABL1-positive ALL. Further advances in the taxonomy of ALL and the discovery of new genetic biomarkers and therapeutic targets, as well as the introduction of targeted and immunotherapies into the frontline treatment protocols, may improve management and outcome of children with ALL. In this review we describe the current developments in the (cyto)genetic diagnostics and management of children with ALL, and provide an overview of the most important advances in the genetic classification of ALL. Furthermore, we discuss perspectives resulting from the development of new techniques, including artificial intelligence (AI).

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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
42
审稿时长
35 days
期刊介绍: Best Practice & Research Clinical Haematology publishes review articles integrating the results from the latest original research articles into practical, evidence-based review articles. These articles seek to address the key clinical issues of diagnosis, treatment and patient management. Each issue follows a problem-orientated approach which focuses on the key questions to be addressed, clearly defining what is known and not known, covering the spectrum of clinical and laboratory haematological practice and research. Although most reviews are invited, the Editor welcomes suggestions from potential authors.
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