阿替唑单抗
非酒精性脂肪性肝炎
贝伐单抗
医学
非酒精性脂肪肝
肝细胞癌
病因学
胃肠病学
代谢综合征
酒精性肝病
内科学
肿瘤科
脂肪肝
疾病
肝硬化
肥胖
化疗
癌症
无容量
免疫疗法
作者
Josep M. Llovet,Mathias Heikenwälder
标识
DOI:10.1053/j.gastro.2023.04.014
摘要
Our studies reporting the survival impact of immune-checkpoint inhibitors (ICIs) in nonalcoholic steatohepatitis (NASH)-associated hepatocellular carcinoma (HCC)1,2 have generated an important debate in the liver cancer field. This is critical given the growing global pandemic of obesity, metabolic syndrome, and nonalcoholic fatty liver disease and the increase in HCC cases related to NASH etiology.3 A recently published Research Letter by Espinoza et al4 in Gastroenterology provides results of the Imbrave 150 for 100 patients with nonviral etiology allocated to the atezolizumab plus bevacizumab arm, readjudicating them to alcohol etiology (n = 51), NASH etiology (n = 47), or unknown (n = 3).
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