急性髓系白血病发病时发热对预后的影响:一项回顾性队列研究。

IF 2.2 4区 医学 Q3 HEMATOLOGY
Leukemia & Lymphoma Pub Date : 2025-08-01 Epub Date: 2025-04-17 DOI:10.1080/10428194.2025.2493342
Eran Levanon, Ido Peles, Eran Meyer, Etai Tarab, Idan Giterman, Yehonatan Sherf, Uri Greenbaum, Tzvika Porges
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引用次数: 0

摘要

发热是急性髓性白血病(AML)的常见临床特征,但其在化疗开始前的预后意义尚不清楚。这项基于人群的回顾性研究分析了2013年至2023年以色列南部的198例AML患者。28.3%的患者出现发热,并伴有较高的1年(53.5% vs. 45.1%, p = 0.030)和5年死亡率(67.8% vs. 57.0%, p = 0.017)。多变量分析显示,发热≥38°C增加1年死亡风险(OR 1.39, 95% CI 1.06-2.58, p = 0.05),发热≥39°C增加至1.93 (95% CI 1.17-2.95, p = 0.02)。发热患者的中位无事件生存期较短(HR 1.63, 95% CI 1.14-2.35, p = 0.008),发热≥39°C患者的中位无事件生存期更短(HR 2.08, 95% CI 1.23-3.53, p = 0.006)。发热与预后的关系因年龄和感染状况而异。这些发现表明,出现发热可能是急性髓性白血病预后不良的临床标志,需要更密切的监测和量身定制的管理,以改善结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic impact of fever at presentation in acute myeloid leukemia: a retrospective cohort study.

Fever at presentation is a common clinical feature in acute myeloid leukemia (AML), yet its prognostic significance before chemotherapy initiation remains unclear. This retrospective, population-based study analyzed 198 AML patients in southern Israel from 2013 to 2023. Fever was present in 28.3% of patients and was associated with higher one-year (53.5% vs. 45.1%, p = 0.030) and five-year mortality rates (67.8% vs. 57.0%, p = 0.017). Multivariable analysis showed that fever ≥38 °C increased one-year mortality risk (OR 1.39, 95% CI 1.06-2.58, p = 0.05), rising to 1.93 for fever ≥39 °C (95% CI 1.17-2.95, p = 0.02). Median event-free survival was shorter in febrile patients (HR 1.63, 95% CI 1.14-2.35, p = 0.008), with greater association at fever ≥39 °C (HR 2.08, 95% CI 1.23-3.53, p = 0.006). Fever's prognostic association varied by age and infection status. These findings suggest that fever at presentation may serve as a clinical marker of poor prognosis in AML, warranting closer monitoring and tailored management to improve outcomes.

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来源期刊
Leukemia & Lymphoma
Leukemia & Lymphoma 医学-血液学
CiteScore
4.10
自引率
3.80%
发文量
384
审稿时长
1.8 months
期刊介绍: Leukemia & Lymphoma in its fourth decade continues to provide an international forum for publication of high quality clinical, translational, and basic science research, and original observations relating to all aspects of hematological malignancies. The scope ranges from clinical and clinico-pathological investigations to fundamental research in disease biology, mechanisms of action of novel agents, development of combination chemotherapy, pharmacology and pharmacogenomics as well as ethics and epidemiology. Submissions of unique clinical observations or confirmatory studies are considered and published as Letters to the Editor
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