Outcome scoring systems for locoregional therapy in hepatocellular carcinoma: a systematic review

医学 列线图 内科学 肝细胞癌 一致性 接收机工作特性 肿瘤科 肝硬化 阶段(地层学) 人口 荟萃分析 肝癌 肝细胞癌 总体生存率 癌症 多元分析 梅德林 生存分析 风险评估 前瞻性队列研究 曲线下面积 肝功能 计分系统 置信区间 缓和医疗 性能状态 试验预测值 预后变量
作者
Cyrus Daruwalla,Evelyn Calderon,Christo Mathew,Lauren Mignogna,Ajit Vyas,David Sada,Rayhan Hai,Benjamin Hines,Muzammil Hanif,Ewout W. Steyerberg,Hashem B. El‐Serag,Rubén Hernáez
出处
期刊:Gut [BMJ]
卷期号:: gutjnl-2025
标识
DOI:10.1136/gutjnl-2025-337557
摘要

Background Locoregional therapy (LRT) is frequently used as bridging therapy to transplantation/resection or palliative treatment for hepatocellular carcinoma (HCC). Multiple prediction models have been developed for prognosis and treatment response among patients undergoing LRTs. Objective We aimed to systematically review the methodological quality and performance of clinical risk scores predicting outcomes in patients with HCC treated with LRT. Design EMBASE and PubMed were searched from inception to 18 March 2026. Our main outcome was the concordance statistic, or area under the receiver operating characteristic curve (AUROC), to predict survival and other tumour-related and liver-related outcomes. Results 130 studies met the inclusion criteria, resulting in 179 individual scoring systems. The total population was 70 061 patients, 21% female (4–51%), most with Barcelona Clinic Liver Cancer Stage B (39%). Risk scores commonly incorporated tumour parameters, liver function tests, cirrhosis staging and comorbidities. AUROC values ranged from 0.56 to 0.94. 16 studies (12.3%) had low risk of bias, while most had high risk of bias. Of these, the Y-scoring system, Cheng et al nomogram and Li et al nomogram showed the highest discrimination for overall survival in palliative LRT (AUROC >0.87). Separate pooled analyses showed that the Hepatoma Arterial-embolisation Prognostic (HAP) and modified Hepatoma Arterial-embolisation Prognostic II (mHAP-II) scores had the highest performance (pooled AUROC >0.72), while the Six-and-Twelve (0.68) and Albumin-Bilirubin (ALBI) scores (0.60) demonstrated lower performance. Conclusion Several outcome scoring systems are promising for specific LRTs and populations. However, most models have high risk of bias, underscoring the need for further development and validation.
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