继发性噬血细胞性淋巴组织细胞病(HLH)诊断和治疗模式的现状展望。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Leonard Naymagon, Philip Roehrs, Michelle Hermiston, James Connelly, Jeffrey Bednarski, Jaap-Jan Boelens, Shanmuganathan Chandrakasan, Blachy Dávila Saldaña, Michael M Henry, Prakash Satwani, Anish Ray, Kelly Walkovich, David Teachey, Edward M Behrens, Scott W Canna, Ashish Kumar
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引用次数: 0

摘要

临床医生对噬血细胞淋巴组织细胞增多症(HLH)认识的提高导致了其诊断的增加。通常根据HLH- 2004标准进行诊断。虽然这些标准有相当大的优势,但它们缺乏特异性,可能在许多促炎疾病的环境中得到满足。影响细胞毒性的遗传缺陷导致家族性(原发性)HLH。另一方面,继发性HLH更多的是许多条件下共同的病理生理过程,而不是单一的疾病实体。遗传、免疫和功能检测的改进不仅改变了我们诊断HLH的方式,也改变了我们治疗HLH的方式。在2004年,几乎没有有效的药物和治疗方案。2024年,有多种安全有效的靶向治疗。我们已经开始认识到,在继发性HLH中常规和立即使用依托泊苷为基础的治疗可能是不合适的,而新兴的细胞因子定向治疗可能是更合理的干预措施。此外,人们认识到,识别和治疗继发性HLH的驱动因素至少与治疗细胞因子风暴和免疫失调同样重要。不幸的是,过度依赖和狭隘地解释《卫生健康报告- 2004》标准可能导致过度诊断、误诊和不必要地接触可能有害的药物。重要的是,临床医生要了解继发性HLH当前诊断模式的局限性,以及依托泊苷基础治疗的反射性使用的缺点。在此,我们将讨论当前识别、诊断和治疗继发性HLH的范例的利弊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perspectives on the current diagnostic and treatment paradigms in secondary hemophagocytic lymphohistiocytosis (HLH).

Improved awareness of hemophagocytic lymphohistiocytosis (HLH) among clinicians has led to an increase in its diagnosis. Often diagnosis is made based on the HLH- 2004 criteria. While these criteria have considerable strengths, they lack specificity and may be fulfilled in the setting of many pro-inflammatory disorders. Genetic defects affecting cellular cytotoxicity cause familial (primary) HLH. On the other hand, secondary HLH is more a pathophysiologic process common to many conditions, rather than a singular disease entity. Improved genetic, immunologic, and functional testing have changed not only the way we diagnose HLH, but also how we treat it. In 2004, there were few active agents and regimens. In 2024, there are multiple safe and effective targeted therapies. We have begun to understand that routine and immediate use of etoposide-based therapy in secondary HLH is likely not appropriate, and emerging cytokine-directed therapies may be more rational interventions. Moreover, it is recognized that identifying and treating the driver of secondary HLH is at least as important as treating the cytokine storm and immune dysregulation. Unfortunately, over-reliance on, and narrow interpretation of, the HLH- 2004 criteria can lead to overdiagnosis, misdiagnosis, and unneeded exposure to drugs that can be harmful. It is important that clinicians understand the limitations of the current diagnostic paradigms for secondary HLH, and the shortcomings of reflexive use of etoposide-based therapy. Herein we will discuss the pros and cons of the current paradigm for the recognition, diagnosis, and treatment of secondary HLH.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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