Mi Ke, Ye Tingdan, Zhu Lin, Pan Calvin Q
Center of Liver Diseases, Beijing Ditan Hospital, Capital Medical University, Beijing, P. R. China.
Division of Gastroenterology and Hepatology, Department of Medicine, NYU Langone Health, New York University Grossman School of Medicine, New York, NY, USA.
Gastroenterol Rep (Oxf). 2025 Feb 20;13:goaf018. doi: 10.1093/gastro/goaf018. eCollection 2025.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is rapidly emerging as the leading global liver disorder and is poised to become the primary cause of hepatocellular carcinoma (HCC). Research indicates that nearly 50% of HCC cases in MASLD patients occur without cirrhosis, often presenting with more advanced and larger tumors. Despite this, current guidelines primarily focus on HCC screening in cirrhotic patients, with limited guidance for non-cirrhotic MASLD individuals. This narrative review seeks to identify key risk factors for HCC development, consolidate available screening methods, and propose a practical, risk-stratified algorithm for HCC surveillance in non-cirrhotic MASLD patients. We conducted a comprehensive review of studies published between 2017 and 2023 using PubMed, Embase, and CNKI, focusing on HCC risk factors and emerging screening strategies for non-cirrhotic MASLD cohorts. Key risk factors for HCC development in these patients include male sex, age over 65, hypertension, diabetes, mild alcohol consumption, smoking, dyslipidemia, elevated alanine aminotransferase levels, and a platelet count ≤ 150 × 10/L. Among the screening methods evaluated, circulating free DNA, alpha-fetoprotein (AFP) combined with protein induced by vitamin K absence or antagonist-II (PIVKA-II), and the GALAD score (incorporating Glypican-3, AFP, alpha-1-Antitrypsin, and des-gamma-carboxy prothrombin) demonstrated the highest performance. Based on these findings, we proposed a risk-stratified HCC surveillance algorithm that integrates GALAD and PIVKA-II into the existing sonography and AFP screening protocols. This review aims to provide clinicians with actionable recommendations for HCC screening in non-cirrhotic MASLD patients.
代谢功能障碍相关脂肪性肝病(MASLD)正迅速成为全球主要的肝脏疾病,并有可能成为肝细胞癌(HCC)的主要病因。研究表明,MASLD患者中近50%的HCC病例发生在无肝硬化的情况下,通常表现为更晚期、更大的肿瘤。尽管如此,目前的指南主要侧重于肝硬化患者的HCC筛查,对非肝硬化MASLD个体的指导有限。这篇叙述性综述旨在确定HCC发生的关键危险因素,整合现有的筛查方法,并为非肝硬化MASLD患者的HCC监测提出一种实用的、基于风险分层的算法。我们使用PubMed、Embase和CNKI对2017年至2023年间发表的研究进行了全面综述,重点关注非肝硬化MASLD队列的HCC危险因素和新兴筛查策略。这些患者发生HCC的关键危险因素包括男性、65岁以上、高血压、糖尿病、轻度饮酒、吸烟、血脂异常、丙氨酸转氨酶水平升高以及血小板计数≤150×10⁹/L。在所评估的筛查方法中,循环游离DNA、甲胎蛋白(AFP)联合维生素K缺乏或拮抗剂-II诱导蛋白(PIVKA-II)以及GALAD评分(包括磷脂酰肌醇蛋白聚糖-3、AFP、α-1抗胰蛋白酶和异常凝血酶原)表现出最高的性能。基于这些发现,我们提出了一种基于风险分层的HCC监测算法,该算法将GALAD和PIVKA-II整合到现有的超声检查和AFP筛查方案中。这篇综述旨在为临床医生提供针对非肝硬化MASLD患者进行HCC筛查的可行建议。