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低白蛋白血症作为急性髓系白血病患者更高死亡率和治疗并发症的预后生物标志物。

Hypoalbuminemia as a prognostic biomarker for higher mortality and treatment complications in acute myeloid leukemia.

机构信息

Division of Hematology/Oncology, Georgetown University Hospital, Lombardi Comprehensive Cancer Center, Washington, DC, USA.

Department of Medicine, University of Washington, Seattle, Washington, USA.

出版信息

Hematol Oncol. 2021 Dec;39(5):697-706. doi: 10.1002/hon.2925. Epub 2021 Sep 9.

DOI:10.1002/hon.2925
PMID:34499366
Abstract

Older age and poor performance status lead to worse outcomes in acute myeloid leukemia (AML) patients. Hypoalbuminemia is a negative predictor of morbidity and mortality in several malignancies. We evaluated the relationship between baseline serum albumin levels on treatment-related complications, as well as short-term mortality and overall survival (OS) in 756 newly diagnosed AML patients. We conducted a retrospective multicenter study to examine treatment-related complications and OS according to pretreatment serum albumin levels: normal albumin ≥3.5 g/dl, marked hypoalbuminemia <2.5 g/dl, and hypoalbuminemia 2.5-3.4 g/dl. In an adjusted multivariate analysis, a lower baseline albumin was independently associated with a higher number of grade ≥3 complications when adjusting for age, secondary AML, sex and intensive treatment. When comparing normal to markedly low albumin levels, the estimated mean number of complications increases by a factor of 1.35. Patients who had a normal baseline albumin had a 30 day-mortality rate of 4.8%, which was significantly lower compared with patients with hypoalbuminemia (16.5%) and marked hypoalbuminemia (33.9%; p < 0.01). Similarly, 60-day mortality rate was significantly higher in the hypoalbuminemia group (24.0%) and marked hypoalbuminemia group (45%) compared with normal albumin group (8.3%; p < 0.01). Patients with lower baseline albumin levels have increased treatment-related morbidity and mortality, suggesting that pre-treatment serum albumin is an important independent prognostic marker.

摘要

老年和较差的体能状态导致急性髓系白血病 (AML) 患者的预后更差。低白蛋白血症是多种恶性肿瘤发病率和死亡率的负预测因子。我们评估了 756 例新诊断的 AML 患者的基线血清白蛋白水平与治疗相关并发症之间的关系,以及短期死亡率和总生存期 (OS)。我们进行了一项回顾性多中心研究,根据预处理血清白蛋白水平检查治疗相关并发症和 OS:正常白蛋白 ≥3.5 g/dl、显著低白蛋白血症 <2.5 g/dl 和低白蛋白血症 2.5-3.4 g/dl。在调整后的多变量分析中,在校正年龄、继发性 AML、性别和强化治疗后,较低的基线白蛋白与更高的≥3 级并发症数量独立相关。当将正常白蛋白与显著低白蛋白水平进行比较时,估计的并发症数量增加了 1.35 倍。基线白蛋白正常的患者 30 天死亡率为 4.8%,明显低于低白蛋白血症(16.5%)和显著低白蛋白血症(33.9%)患者(p<0.01)。同样,低白蛋白血症组(24.0%)和显著低白蛋白血症组(45%)的 60 天死亡率明显高于正常白蛋白血症组(8.3%)(p<0.01)。基线白蛋白水平较低的患者治疗相关发病率和死亡率增加,表明治疗前血清白蛋白是一个重要的独立预后标志物。

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