Rivera-Esteban Jesús, Muñoz-Martínez Sergio, Higuera Mónica, Sena Elena, Bermúdez-Ramos María, Bañares Juan, Martínez-Gomez María, Cusidó M Serra, Jiménez-Masip Alba, Francque Sven M, Tacke Frank, Minguez Beatriz, Pericàs Juan M
Liver Unit, Department of Internal Medicine, Vall d'Hebron University Hospital, Barcelona, Spain; Vall d'Hebron Institut de Recerca, Vall d'Hebron Barcelona Campus Hospitalari, Barcelona, Spain; Department of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain.
Vall d'Hebron Institut de Recerca, Vall d'Hebron Barcelona Campus Hospitalari, Barcelona, Spain; Universitat de Barcelona, Barcelona, Spain.
Clin Gastroenterol Hepatol. 2024 Sep;22(9):1774-1789.e8. doi: 10.1016/j.cgh.2024.03.028. Epub 2024 Apr 10.
Hepatocellular carcinoma (HCC) typically develops as a consequence of liver cirrhosis, but HCC epidemiology has evolved drastically in recent years. Metabolic dysfunction-associated steatotic liver disease (MASLD), including metabolic dysfunction-associated steatohepatitis, has emerged as the most common chronic liver disease worldwide and a leading cause of HCC. A substantial proportion of MASLD-associated HCC (MASLD-HCC) also can develop in patients without cirrhosis. The specific pathways that trigger carcinogenesis in this context are not elucidated completely, and recommendations for HCC surveillance in MASLD patients are challenging. In the era of precision medicine, it is critical to understand the processes that define the profiles of patients at increased risk of HCC in the MASLD setting, including cardiometabolic risk factors and the molecular targets that could be tackled effectively. Ideally, defining categories that encompass key pathophysiological features, associated with tailored diagnostic and treatment strategies, should facilitate the identification of specific MASLD-HCC phenotypes. In this review, we discuss MASLD-HCC, including its epidemiology and health care burden, the mechanistic data promoting MASLD, metabolic dysfunction-associated steatohepatitis, and MASLD-HCC. Its natural history, prognosis, and treatment are addressed specifically, as the role of metabolic phenotypes of MASLD-HCC as a potential strategy for risk stratification. The challenges in identifying high-risk patients and screening strategies also are discussed, as well as the potential approaches for MASLD-HCC prevention and treatment.
肝细胞癌(HCC)通常是由肝硬化发展而来,但近年来HCC的流行病学已发生了巨大变化。代谢功能障碍相关脂肪性肝病(MASLD),包括代谢功能障碍相关脂肪性肝炎,已成为全球最常见的慢性肝病和HCC的主要病因。相当一部分与MASLD相关的HCC(MASLD-HCC)也可在无肝硬化的患者中发生。在这种情况下引发致癌作用的具体途径尚未完全阐明,对MASLD患者进行HCC监测的建议也颇具挑战性。在精准医学时代,了解在MASLD背景下确定HCC风险增加患者特征的过程至关重要,包括心脏代谢危险因素和可有效应对的分子靶点。理想情况下,定义包含关键病理生理特征的类别,并结合量身定制的诊断和治疗策略,应有助于识别特定的MASLD-HCC表型。在本综述中,我们讨论了MASLD-HCC,包括其流行病学和医疗负担、促进MASLD、代谢功能障碍相关脂肪性肝炎和MASLD-HCC的机制数据。特别阐述了其自然史、预后和治疗,以及MASLD-HCC代谢表型作为风险分层潜在策略的作用。还讨论了识别高危患者和筛查策略方面的挑战,以及MASLD-HCC预防和治疗的潜在方法。