Singh Amisha, Beechinor Ryan J, Huynh Jasmine C, Li Daneng, Dayyani Farshid, Valerin Jennifer B, Hendifar Andrew, Gong Jun, Cho May
Internal Medicine, University of California, Davis, Sacramento, CA 95817, USA.
UC Davis Comprehensive Cancer Center, Sacramento, CA 95817, USA.
Cancers (Basel). 2021 Apr 30;13(9):2164. doi: 10.3390/cancers13092164.
Hepatocellular carcinoma (HCC) is the second most common cause of cancer death worldwide. HCC tumor development and treatment resistance are impacted by changes in the microenvironment of the hepatic immune system. Immunotherapy has the potential to improve response rates by overcoming immune tolerance mechanisms and strengthening anti-tumor activity in the tumor microenvironment. In this review, we characterize the impact of immunotherapy on outcomes of advanced HCC, as well as the active clinical trials evaluating novel combination immunotherapy strategies. In particular, we discuss the efficacy of atezolizumab and bevacizumab as demonstrated in the IMbrave150 study, which created a new standard of care for the front-line treatment of advanced HCC. However, there are multiple ongoing trials that may present additional front-line treatment options depending on their efficacy/toxicity results. Furthermore, the preliminary data on the application of chimeric antigen receptor (CAR-T) cell therapy for treatment of HCC suggests this may be a promising option for the future of advanced HCC treatment.
肝细胞癌(HCC)是全球第二大常见癌症死亡原因。HCC肿瘤的发展和治疗耐药性受到肝脏免疫系统微环境变化的影响。免疫疗法有潜力通过克服免疫耐受机制和增强肿瘤微环境中的抗肿瘤活性来提高缓解率。在本综述中,我们阐述了免疫疗法对晚期HCC治疗结果的影响,以及评估新型联合免疫疗法策略的正在进行的临床试验。特别是,我们讨论了阿替利珠单抗和贝伐单抗在IMbrave150研究中所显示的疗效,该研究为晚期HCC的一线治疗确立了新的护理标准。然而,有多项正在进行的试验,根据其疗效/毒性结果可能会提供更多一线治疗选择。此外,嵌合抗原受体(CAR-T)细胞疗法治疗HCC的初步数据表明,这可能是晚期HCC治疗未来的一个有前景的选择。