Hepatology and Liver Unit, Hospital Universitario Austral, School of Medicine, Austral University, Buenos Aires B1629HJ, Argentina.
Clinical Oncology, Insituto do Cancer do Estado de São Paulo, University of São Paulo, São Paulo 05403-000, Brazil.
World J Gastroenterol. 2021 Jun 28;27(24):3429-3439. doi: 10.3748/wjg.v27.i24.3429.
Although hepatocellular carcinoma is considered a highly lethal malignancy, recent therapeutic advances have been achieved during the last 10 years. This scenario resulted in an unprecedented improvement in survival for patients with advanced hepatocellular carcinoma, almost reaching 20-26 mo of overall survival after first-second line sequential treatment. The advent of the combination of atezolizumab with bevacizumab showed, for the first time, superiority over sorafenib with improvement in overall survival. However, first and second-line trials were correctly based on the premise that a strict selection of patients enhances the power to capture the positive effect of treatment by excluding competing risks for mortality such as liver failure, decompensated cirrhosis or other underlying medical conditions. As a result, the inclusion criteria used in clinical trials do not support the use of novel therapies in several real-world scenarios involving underrepresented subgroups, such as patients with unpreserved liver function, other comorbid conditions, a history of solid-organ transplantation, autoimmune disorders and those with a high risk of bleeding. The present text aims at discussing treatment strategies in these subgroups.
虽然肝细胞癌被认为是一种高度致命的恶性肿瘤,但在过去的 10 年中,已经取得了最近的治疗进展。这种情况导致晚期肝细胞癌患者的生存率得到了前所未有的提高,在一线和二线序贯治疗后,总生存时间几乎达到 20-26 个月。阿替利珠单抗联合贝伐珠单抗的出现首次显示出优于索拉非尼的优势,改善了总生存。然而,一线和二线试验的正确性基于这样一个前提,即严格选择患者可以通过排除肝衰竭、失代偿性肝硬化或其他潜在医疗状况等导致死亡的竞争风险,增强对治疗效果的捕捉能力。因此,临床试验中使用的纳入标准并不支持在几个涉及代表性不足的亚组的真实世界场景中使用新的治疗方法,例如肝功能未受损、其他合并症、实体器官移植史、自身免疫性疾病和出血风险高的患者。本文旨在讨论这些亚组的治疗策略。