Department of Medicine, University of Padova, 35123 Padova, Italy.
National Institute of Gastroenterology-IRCCS "Saverio de Bellis", 70013 Castellana Grotte, Italy.
Int J Mol Sci. 2023 Nov 18;24(22):16485. doi: 10.3390/ijms242216485.
Hepatocellular carcinoma (HCC) accounts for more than 75% of primary liver cancers, which are the second leading cause of cancer-related deaths. The GALAD (gender, age, AFP-L3, AFP, and des-carboxy-prothrombin) score is a diagnostic tool developed based on gender, age, alpha-fetoprotein, alpha-fetoprotein L3, and des-gamma-carboxy prothrombin, originally designed as a diagnostic tool for HCC in high-risk patients.
We analyzed 212 patients with and without cirrhosis. The population study was divided into patients with liver cirrhosis without evidence of HCC at the time of serum sample collection for GALAD score determination and patients with liver cirrhosis and a confirmed diagnosis of HCC at the time of serum sample collection for GALAD score determination. Patients were followed up until death or liver transplantation. The association between variables and HCC mortality risk was performed, and the results were presented as hazard ratio (HR). The receiver operating characteristic (ROC) curve was used to assess the performance of the GALAD HCC diagnosis. The survival probability was explored using the non-parametric test, and the equality of survival amongst categories was assessed with the log-rank test.
Biomarkers were higher in the HCC group compared to cirrhosis. Kaplan-Meier survival probability analysis for individual GALAD categories revealed that a high GALAD level was associated with decreased survival during follow-up, and the difference between the curves was statistically significant ( = 0.01).
Our findings suggest that the GALAD score has promise as a prognostic tool, with implications for improving patient management and treatment strategies for HCC.
肝细胞癌(HCC)占原发性肝癌的 75%以上,是癌症相关死亡的第二大主要原因。GALAD(性别、年龄、AFP-L3、AFP 和脱羧基凝血酶原)评分是一种基于性别、年龄、甲胎蛋白、甲胎蛋白 L3 和脱羧基凝血酶原开发的诊断工具,最初是为高危患者的 HCC 设计的诊断工具。
我们分析了 212 例有和无肝硬化的患者。人群研究分为肝硬化患者,在进行 GALAD 评分测定时无 HCC 证据,以及肝硬化患者,在进行 GALAD 评分测定时已确诊 HCC。患者随访至死亡或肝移植。对变量与 HCC 死亡率风险的相关性进行了分析,并以风险比(HR)表示结果。采用接收者操作特征(ROC)曲线评估 GALAD 对 HCC 的诊断性能。采用非参数检验探讨生存概率,对数秩检验评估各分类之间生存的均等性。
与肝硬化组相比,HCC 组的生物标志物更高。对个体 GALAD 分类的 Kaplan-Meier 生存概率分析表明,高 GALAD 水平与随访期间的生存降低相关,曲线之间的差异具有统计学意义(=0.01)。
我们的研究结果表明,GALAD 评分有望成为一种预后工具,对改善 HCC 的患者管理和治疗策略具有重要意义。