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A Review of Current and Emerging Therapeutic Options for Hemophagocytic Lymphohistiocytosis

医学 噬血细胞性淋巴组织细胞增多症 阿勒姆图祖马 托珠单抗 巨噬细胞活化综合征 免疫失调 重症监护医学 阿纳基纳 细胞激素风暴 造血干细胞移植 细胞因子释放综合征 临床试验 疾病 免疫学 免疫系统 2019年冠状病毒病(COVID-19) 嵌合抗原受体 免疫疗法 内科学 传染病(医学专业) 抗体
作者
Jenna Summerlin,Drew A. Wells,Mary Kate Anderson,Zachery Halford
出处
期刊:Annals of Pharmacotherapy [SAGE Publishing]
卷期号:57 (7): 867-879 被引量:12
标识
DOI:10.1177/10600280221134719
摘要

Objective: To provide an overview of clinical sequelae and emerging treatment options for hemophagocytic lymphohistiocytosis (HLH). Data Sources: A literature search was conducted using the search terms “hemophagocytic lymphohistiocytosis,” “hemophagocytic syndrome,” “macrophage activation syndrome,” and “treatment” on Ovid and PubMed from January 1, 2017, through September 28, 2022. Study Selection and Data Extraction: Relevant clinical trials, meta-analyses, case reports, review articles, package inserts, and guidelines to identify current and emerging therapeutic options for the management of HLH. Data Synthesis: Genetic disorders and secondary causes may trigger HLH in both children and adults. Notable improvements in the diagnosis of HLH were seen with implementation of the HLH-2004 standard diagnostic criteria; however, timely and accurate identification of HLH remain significant barriers to optimal management. Multiagent immunochemotherapy are the backbone of aggressive therapy for acutely ill patients with HLH. Relevance to Patient Care and Clinical Practice: The global coronavirus 2019 (COVID-19) pandemic and emerging immune effector cell therapies have served to highlight the concerns with immune dysregulation and subsequent HLH precipitation. Without prompt identification and treatment, HLH can be fatal. Historically, the clinician’s armamentarium for managing HLH was sparse, with etoposide-based protocols serving as the standard of care. Relapsed or refractory disease portends a poor prognosis and requires additional treatment options. Second- or subsequent-line options now include hematopoietic stem cell transplantation, emapalumab, alemtuzumab, anakinra, ruxolitinib, and tocilizumab. Conclusions: Improvements in diagnostic methods and novel immunosuppressive treatment strategies, including noncytotoxic immunochemotherapy, have transformed the therapeutic landscape. Unfortunately, many unanswered questions remain. Additional studies are required to optimize dosing, schedules, treatment sequences, and indications for novel treatment options.
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