HALP评分预测移植后早期预后:一项25年肝细胞癌和肝移植预后的回顾性研究。

IF 0.8
Cihan Agalar, Tufan Egeli, Anil Aysal, Mucahit Ozbilgin, Berkay Sakaoglu, Nilay Danis, Emre Karadeniz, Erhan Tükel, Ibrahim Astarcioglu, Ozgul Sagol, Tarkan Unek
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引用次数: 0

摘要

目的:血红蛋白-白蛋白-淋巴细胞-血小板(HALP)评分是一种与各种恶性肿瘤预后相关的免疫营养指标。然而,其在肝移植(LT)治疗肝细胞癌(HCC)中的预后意义仍未被探索。本研究探讨了HALP评分对HCC患者移植后生存和复发的预后影响。患者和方法:一项回顾性队列研究纳入了1998年至2023年间131例因HCC接受肝移植的患者。根据受试者工作特征(ROC)分析确定的阈值55.689将患者分为高HALP组和低HALP组。采用Kaplan-Meier和Cox回归模型分析总生存期(OS)、无病生存期(DFS)和围手术期死亡率。结果:低HALP组围手术期死亡率(18.3% vs. 5.6%, P = 0.003)、第一年死亡率(30.0% vs. 9.9%, P = 0.001)和三年死亡率(48.3% vs. 22.5%, P = 0.001)均显著高于低HALP组。低HALP组总生存期明显缩短(P = 0.003)。多因素分析发现,低HALP是围手术期(OR: 12.76, P = 0.019; HR: 11.68, P = 0.021)、第一年(OR: 5.19, P = 0.005; HR: 4.22, P = 0.007)和第三年死亡率(OR: 3.67, P = 0.01; HR: 2.88, P = 0.012)的独立危险因素。结论:HALP评分是一种有希望预测肝细胞癌肝移植患者早期风险的预后生物标志物。将HALP纳入移植前评估可以优化患者选择和围手术期管理,改善移植后预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
HALP Score Predicts Early Post-Transplant Outcomes: A 25-Year Retrospective Study on Hepatocellular Carcinoma and Liver Transplantation Outcomes.

Aim: The Hemoglobin-Albumin-Lymphocyte-Platelet (HALP) score is an immune nutritional marker associated with prognosis in various malignancies. However, its prognostic significance in liver transplantation (LT) for hepatocellular carcinoma (HCC) remains unexplored. This study investigates the prognostic impact of the HALP score on post-transplant survival and recurrence in HCC patients.

Patients and methods: A retrospective cohort study included 131 patients who underwent Liver Transplantation for HCC between 1998 and 2023. Patients were stratified into high and low HALP groups based on a threshold value of 55.689 determined via receiver operating characteristic (ROC) analysis. Overall survival (OS), disease-free survival (DFS), and perioperative mortality were analyzed using Kaplan-Meier and Cox regression models.

Results: The low HALP group exhibited significantly higher perioperative mortality (18.3% vs. 5.6%, P = .003), first-year mortality (30.0% vs. 9.9%, P = .001), and three-year mortality (48.3% vs. 22.5%, P = .001). Overall survival was significantly shorter in the low HALP group (P = .003). Multivariate analysis identified low HALP as an independent risk factor for perioperative (OR: 12.76, P = .019; HR: 11.68, P = .021), first-year (OR: 5.19, P = .005; HR: 4.22, P = .007) and third-year mortality (OR: 3.67, P = .01; HR: 2.88, P = .012).

Conclusion: The HALP score is a promising prognostic biomarker for predicting early risk in LT candidates with HCC. Integrating HALP into pre-transplant assessment may optimize patient selection and perioperative management, improving post-transplant outcomes.

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