Clinical characteristics and prognostic factors in patients with fever of unknown origin who developed secondary haemophagocytic lymphohistiocytosis.

IF 3 3区 医学 Q2 HEMATOLOGY
Annals of Hematology Pub Date : 2025-05-01 Epub Date: 2025-02-20 DOI:10.1007/s00277-024-06174-0
Zhe Zhou, Guanmin Yuan, Yang Li, Haocheng Zhang, Shenglei Yu, Lingyun Shao, Jingwen Ai, Wenhong Zhang
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引用次数: 0

Abstract

Background: Patients with fever of unknown origin (FUO) can sometimes be accompanied by haemophagocytic lymphohistiocytosis (HLH), a life-threatening disease. The prognostic model and specific markers for the early prognosis and the optimized treatment regimen are of considerable research interest.

Results: A total of 135 FUO/HLH patients were enrolled and classified according to the 60-day outcomes following diagnosis. 79 patients (including 5 patients lost in follow-up) enrolled from 2007 to 2015 served as the derivation cohort, and 56 patients from 2016 to 2023 served as the validation cohort. In the derivation cohort, 27 patients (27/74, 36.5%) survived within 60 days and multivariate analyses showed that age > 67 years (P = 0.003), baseline PLT < 42 × 10^9/L (P = 0.012) and LDH > 1505 U/L (P = 0.002) were associated with a higher mortality rate in HLH patients. The external validation proved the reliability of the prediction model. In derivation cohort, the median alteration of PLT (△PLT) were + 78 × 10^9/L and - 17 × 10^9/L in the survival and non-survival groups, respectively (P < 0.001). The median △LDH was - 197.5U/L in the survival group, while in the non-survival group was + 119U/L (P < 0.001).

Conclusions: Age, baseline LDH and PLT levels may predict early mortality in secondary HLH patients and identify patients in critical conditions. △LDH and △PLT levels were of high value to monitor the efficacy of therapeutic regimen and the disease progression in HLH patients.

不明原因发热继发嗜血球性淋巴组织细胞增多症患者的临床特点及预后因素分析。
背景:不明原因发热(FUO)患者有时可伴有噬血细胞性淋巴组织细胞增多症(HLH),这是一种危及生命的疾病。早期预后的预后模型和特异性标志物以及优化的治疗方案是目前研究的热点。结果:共纳入135例FUO/HLH患者,并根据诊断后60天的结果进行分类。2007 - 2015年入组的79例患者(包括5例失访患者)为衍生队列,2016 - 2023年入组的56例患者为验证队列。在衍生队列中,27例患者(27/ 74,36.5%)在60天内存活,多因素分析显示,年龄在60至67岁之间(P = 0.003),基线PLT为1505 U/L (P = 0.002)与HLH患者较高的死亡率相关。外部验证证明了预测模型的可靠性。衍生队列中,生存组和非生存组的PLT中位变化(△PLT)分别为+ 78 × 10^9/L和- 17 × 10^9/L。(P)结论:年龄、基线LDH和PLT水平可预测继发性HLH患者的早期死亡,并可识别危重患者。△LDH、△PLT水平对监测HLH患者治疗方案疗效及病情进展具有重要价值。
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
Annals of Hematology
Annals of Hematology 医学-血液学
CiteScore
5.60
自引率
2.90%
发文量
304
审稿时长
2 months
期刊介绍: Annals of Hematology covers the whole spectrum of clinical and experimental hematology, hemostaseology, blood transfusion, and related aspects of medical oncology, including diagnosis and treatment of leukemias, lymphatic neoplasias and solid tumors, and transplantation of hematopoietic stem cells. Coverage includes general aspects of oncology, molecular biology and immunology as pertinent to problems of human blood disease. The journal is associated with the German Society for Hematology and Medical Oncology, and the Austrian Society for Hematology and Oncology.
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