中性粒细胞与淋巴细胞比值和血小板与淋巴细胞比值基线预测非洲黑人晚期肝癌姑息治疗患者住院死亡率的预后价值:一项比较队列研究

IF 2.6 Q2 GASTROENTEROLOGY & HEPATOLOGY
Hepatic Medicine : Evidence and Research Pub Date : 2021-12-08 eCollection Date: 2021-01-01 DOI:10.2147/HMER.S333980
Alassan Kouame Mahassadi, Henriette Anzouan-Kacou Kissi, Alain Koffi Attia
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引用次数: 5

摘要

背景:中性粒细胞与淋巴细胞比值(NLR)和血小板与淋巴细胞比值(PLR)在预测非洲黑人晚期肝细胞癌(HCC)姑息治疗患者住院死亡率中的预后价值尚不清楚。目的:比较NLR和PLR与child - turcot - pugh (CTP)、终末期肝病模型(MELD)评分和巴塞罗那临床肝癌分期系统(BCLC)的预后价值。方法:采用受试者工作特征曲线(AUC)下的时间依赖面积、对数秩检验和Cox比例风险比来确定这些预后评分的截止点、准确性及其与死亡率的相关性。结果:共纳入104例晚期HCC患者(中位年龄49.5岁,男性58.7%)。所有患者均因右胸象限肝脏肿大至少15.4 cm而住院。总体而言,46例(44.2%)患者在随访期间在医院死亡。NLR >2.5 (log rank检验=7.11,p=0.01)或PLR >92 (log rank检验=5.63,p=0.02)的患者生存较差。与住院死亡率相关的因素是MELD评分(p=0.01)、NLR (p=0.03)和血红蛋白水平(p=0.02)。NLR在随访30天(AUC=0.618)、60天(AUC=0.680)和90天(AUC=0.613)时预测院内死亡率的准确性优于CTP、MELD评分、BCLC和PLR。然而,在90天的随访中,PLR显示出更高的准确性(AUC=0.688)。结论:NLR可用于预测黑非洲晚期肝癌患者的住院死亡率。NLR和PLR可同时用于长期随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Prognostic Values of Neutrophil-to-lymphocyte Ratio and Platelet-to-Lymphocyte Ratio at Baseline in Predicting the In-hospital Mortality in Black African Patients with Advanced Hepatocellular Carcinoma in Palliative Treatment: A Comparative Cohort Study.

The Prognostic Values of Neutrophil-to-lymphocyte Ratio and Platelet-to-Lymphocyte Ratio at Baseline in Predicting the In-hospital Mortality in Black African Patients with Advanced Hepatocellular Carcinoma in Palliative Treatment: A Comparative Cohort Study.

The Prognostic Values of Neutrophil-to-lymphocyte Ratio and Platelet-to-Lymphocyte Ratio at Baseline in Predicting the In-hospital Mortality in Black African Patients with Advanced Hepatocellular Carcinoma in Palliative Treatment: A Comparative Cohort Study.

Background: The prognostic values of the neutrophil-to-lymphocyte ratio (NLR) and the platelet-to-lymphocyte ratio (PLR) in predicting the in-hospital mortality of Black African patients with advanced hepatocellular carcinoma (HCC) in palliative treatment is unknown.

Aim: To determine the prognostic value of NLR and PLR compared with that of Child-Turcotte-Pugh (CTP), model for end-stage liver disease (MELD) scores and the Barcelona clinic liver cancer staging system (BCLC).

Methods: The cutoffs, accuracies and association with the mortality of these prognostic scores were determined using a time-dependent area under receiver operating characteristic curves (AUC), the log rank test and Cox proportional hazards ratio.

Results: A total of 104 patients with advanced HCC (median age=49.5 years, males=58.7%) were enrolled. All were hospitalized for an enlarged liver mass of at least 15.4 cm in size in the right thoracic quadrant. Overall, 46 (44.2%) patients died in hospital during follow-up. Patients with NLR >2.5 (log rank test=7.11, p=0.01) or PLR >92 (log rank test=5.63, p=0.02) had poor survival. Factors associated with the in-hospital mortality were the MELD score (p=0.01), NLR (p=0.03) and hemoglobin level (p=0.02). NLR exhibits better and stable accuracy in predicting the in hospital mortality at time points of 30 (AUC=0.618), 60 (AUC=0.680) and 90 (AUC=0.613) days of follow-up, compared with CTP, MELD scores, BCLC and PLR. However, PLR displayed an enhanced accuracy over 90 days of follow up (AUC=0.688).

Conclusion: NLR is useful in predicting the in-hospital mortality in Black African patients with advanced stage HCC in clinical practice. NLR and PLR may be used concomitantly for long-term follow-up.

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来源期刊
Hepatic Medicine : Evidence and Research
Hepatic Medicine : Evidence and Research GASTROENTEROLOGY & HEPATOLOGY-
自引率
0.00%
发文量
15
审稿时长
16 weeks
期刊介绍: Hepatic Medicine: Evidence and Research is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of adult and pediatric hepatology in the clinic and laboratory including the following topics: Pathology, pathophysiology of hepatic disease Investigation and treatment of hepatic disease Pharmacology of drugs used for the treatment of hepatic disease Although the main focus of the journal is to publish research and clinical results in humans; preclinical, animal and in vitro studies will be published where they will shed light on disease processes and potential new therapies. Issues of patient safety and quality of care will also be considered. As of 1st April 2019, Hepatic Medicine: Evidence and Research will no longer consider meta-analyses for publication.
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