接受姑息治疗的晚期癌症患者与c反应蛋白和白蛋白相关的炎症生物标志物的变化:一项纵向研究

E. Wiegert, L. Calixto-Lima, G. Cunha, Tais Saint Martin Fonseca, G. Silva, L. C. de Oliveira
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引用次数: 0

摘要

背景:关于炎症生物标志物在终末期癌症发展过程中如何变化的证据尚缺乏。本研究探讨了接受姑息治疗的晚期癌症患者在生命最后三个月内白蛋白和c反应蛋白(CRP)水平以及CRP/白蛋白比(CAR)的纵向变化。方法:这是从一项前瞻性队列研究中提取的变量进行回顾性分析,该研究包括巴西国家癌症研究所独家姑息治疗单元的住院患者。记录死亡前0 ~ 15天(T1)、16 ~ 30天(T2)、31 ~ 45天(T3)、46 ~ 60天(T4)、61 ~ 75天(T5)、76 ~ 90天(T6)血常规白蛋白、CRP检查结果,且只纳入至少两次检查的患者。采用粗糙和调整后的线性混合效应回归模型来验证生物标志物的纵向轨迹与死亡之间的关系。结果:共纳入1635例患者。在整个分析时间内,白蛋白的中位数为3.00g/dL(四分位数范围,IQR: 2.50-3.60),随着死亡的临近而下降,而CRP的中位数为9.31mg/L (IQR: 4.42-17.30), CAR为3.20 (IQR: 1.40-6.60),两者均升高。白蛋白(斜率:0.01 ~ 0.02;p <0.001), CRP(斜率:-0.10 ~ -0.12;p <0.001), CAR(斜率:-0.06;P <0.001),在粗模型和校正模型中显示与死亡呈线性剂量-反应关系。结论:炎症生物标志物的纵向变化水平随着死亡的临近而恶化,可用于预测晚期癌症患者的终末期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Inflammatory Biomarkers Related to C-reactive Protein and Albumin in Patients With Terminal Cancer Receiving Palliative Care: a Longitudinal Study
Background: Evidence about how inflammatory biomarkers vary during the end-stage cancer trajectory is lacking. This study investigates the longitudinal changes in albumin and C-reactive protein (CRP) levels, and CRP/albumin ratio (CAR) in patients with terminal cancer receiving palliative care in the last three months of life.Methods: This is a retrospective analysis of variables extracted from a prospective cohort study that included admitted patients to the exclusive Palliative Care Unit of the National Cancer Institute in Brazil. Routine blood examination results of albumin and CRP were recorded at 0-15 (T1), 16-30 (T2), 31-45 (T3), 46-60 (T4), 61-75 (T5), and 76-90 (T6) days before death and only patients with at least two measurements were included. Crude and adjusted linear mixed-effects regression models were performed to verify the relationships between the longitudinal trajectories of biomarkers and death. Results: A total of 1,635 patients were included. Median albumin was 3.00g/dL across the whole time-period analyzed (interquartile range, IQR: 2.50-3.60) and decreased with the approach of death, while median CRP was 9.31mg/L (IQR: 4.42-17.30) and CAR was 3.20 (IQR: 1.40-6.60), and both increased. The albumin (slope: 0.01 to 0.02; p <0.001), CRP (slope: -0.10 to -0.12; p <0.001), and CAR (slope: -0.06; p <0.001) showed a linear dose-response relationship with death in crude and adjusted models tested. Conclusions: The longitudinal change levels of inflammatory biomarkers worsen with the approach of death and could be used to predict end-stage in patients with terminal cancer.
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