Flow cytometry in the diagnosis of myelodysplastic syndromes

IF 2.3 3区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Wolfgang Kern, Arjan van de Loosdrecht
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引用次数: 0

Abstract

In hematologic neoplasms, the identification of recurrent disease-associated phenotypic features in general is followed after a prolonged period by the identification of disease-associated and even disease-defining genetic changes based on which specific treatment will be developed. As an example, for chronic myelogenous leukemia (CML) this has taken one and a half century from the first publication on morphology (Virchow, 1845) to the first report on a tyrosin-kinase inhibitor (Druker et al., 2001). For myelodysplastic syndromes (MDS) the interval between publication of morphologic classification system (Bennett et al., 1982) and the most recent WHO classification applying genetic criteria for diagnostics (Khoury et al., 2022) the interval has been significantly shorter. For various reasons, the role of immunophenotypic features of MDS and their flow cytometric identification had been neglected for a long time.

Following pivotal publication on the topic by Denise Wells and Mike Loken (Wells et al., 2003) flow cytometrists became increasingly interested and gathered together in 2007 at the MDS Foundation Conference in Florence, Italy, which proved to be the founding hour of the “ELN iMDS flow working group.” Each member of the group has focused their research on assessing the diagnostic application of flow cytometry in MDS. Since 2007, the ELN iMDS flow working group has held yearly meetings to discuss progress in research activities as well as to divise consensus guideline publications aiming to apply flow cytometry in a valid manner for in the diagnostic setting of MDS (Porwit, 2014; van de Loosdrecht et al., 2009; van de Loosdrecht et al., 2013; Westers et al., 2012; Westers et al., 2017). These meetings allowed not only for continuous scientific discussion between experts from worldwide (i.e., although formed under the roof of the European LeukemiaNet members came from North America, Europe, Asia and Australia) but also for friendships reaching beyond any scientific scope.

This Special Issue of Clinical Cytometry on the application of flow cytometry in the diagnostic setting of MDS comprises a variety of different papers from the ELN iMDS flow working group reaching from updated consensus guidelines over multi center studies to research results generated by the members of the group. It has been our pleasure to coordinate this group for one and a half decades and we hope the readers of the Special Issue enjoy reading the articles and get stimulated to add their research to the topic.

Wolfgang Kern declares part ownership of MLL Munich Leukemia Laboratory.

流式细胞术在骨髓增生异常综合征诊断中的应用
在血液学肿瘤中,通常在确定复发性疾病相关的表型特征之后,经过很长一段时间,确定疾病相关甚至疾病定义的遗传变化,从而开发特异性治疗。例如,对于慢性髓性白血病(CML),从首次发表形态学(Virchow, 1845)到首次报道酪氨酸激酶抑制剂(Druker et al., 2001),已经花了一个半世纪的时间。对于骨髓增生异常综合征(MDS),从形态学分类系统(Bennett et al., 1982)的发表到应用遗传诊断标准的最新WHO分类(Khoury et al., 2022)的间隔时间明显缩短。由于种种原因,MDS的免疫表型特征及其流式细胞术鉴定的作用长期被忽视。在Denise Wells和Mike Loken (Wells等人,2003年)发表了关于这一主题的重要文章之后,流式细胞仪学家对这一主题越来越感兴趣,并于2007年在意大利佛罗伦萨举行的MDS基金会会议上聚集在一起,这被证明是“ELN iMDS流动工作组”的成立时刻。每个小组成员都专注于评估流式细胞术在MDS中的诊断应用。自2007年以来,ELN iMDS流动工作组每年召开会议,讨论研究活动的进展,并就旨在有效地将流式细胞术应用于MDS诊断环境的共识指南出版物进行划分(Porwit, 2014;van de Loosdrecht et al., 2009;van de Loosdrecht et al., 2013;Westers et al., 2012;韦斯特等人,2017)。这些会议不仅允许来自世界各地的专家之间进行持续的科学讨论(即,尽管是在欧洲白血病网的屋檐下形成的,但来自北美、欧洲、亚洲和澳大利亚的成员),而且还允许超越任何科学范围的友谊。《临床细胞术》特刊关于流式细胞术在MDS诊断中的应用,包括来自ELN iMDS流式工作小组的各种不同论文,从多中心研究的最新共识指南到小组成员产生的研究结果。我们很高兴能在十五年的时间里协调这个小组,我们希望特刊的读者喜欢阅读这些文章,并受到激励,将他们的研究添加到这个主题中。沃尔夫冈·科恩宣布MLL慕尼黑白血病实验室部分所有权。
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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来源期刊
CiteScore
6.80
自引率
32.40%
发文量
51
审稿时长
>12 weeks
期刊介绍: Cytometry Part B: Clinical Cytometry features original research reports, in-depth reviews and special issues that directly relate to and palpably impact clinical flow, mass and image-based cytometry. These may include clinical and translational investigations important in the diagnostic, prognostic and therapeutic management of patients. Thus, we welcome research papers from various disciplines related [but not limited to] hematopathologists, hematologists, immunologists and cell biologists with clinically relevant and innovative studies investigating individual-cell analytics and/or separations. In addition to the types of papers indicated above, we also welcome Letters to the Editor, describing case reports or important medical or technical topics relevant to our readership without the length and depth of a full original report.
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