Atezolizumab-bevacizumab plus Y-90 TARE for the treatment of hepatocellular carcinoma: preclinical rationale and ongoing clinical trials

阿替唑单抗 医学 免疫疗法 贝伐单抗 封锁 肝细胞癌 肿瘤科 免疫检查点 肿瘤微环境 内科学 癌症 癌症研究 无容量 化疗 受体
作者
Alessandro Di Federico,Alessandro Rizzo,Riccardo Carloni,Andrea De Giglio,R. Bruno,Dalia Ricci,Giovanni Brandi
出处
期刊:Expert Opinion on Investigational Drugs [Informa]
卷期号:31 (4): 361-369 被引量:68
标识
DOI:10.1080/13543784.2022.2009455
摘要

The treatment algorithm of advanced hepatocellular carcinoma (HCC) has evolved since the introduction of immunotherapy. The IMbrave150 trial set atezolizumab-bevacizumab as a new standard-of-care first-line treatment for unresectable HCC patients. However, for patients with intermediate or advanced stage with portal vein thrombosis but without distant metastases, 90Yttrium transarterial radioembolization (90Y-TARE) is considered the treatment of choice.We discuss the main evidence regarding the use of 90Y-TARE in HCC, the recent progress of immunotherapy in this tumor, and the preclinical rationale of combining VEGF blockade with the other two treatment strategies.HCC has an extremely heterogeneous tumor immune microenvironment. This may explain the inconsistent outcomes obtained with immune-checkpoint inhibitors. The identification of patients who could benefit most from immunotherapy is crucial; however, reliable markers of response are lacking. Radiation therapy and VEGF inhibition have an established synergism with immunotherapy, mainly linked to enhanced antigen presentation and reduced immunosuppressive immune infiltrate. Combining an immune-checkpoint inhibitor with VEGF blockade and 90Y-TARE might hence overcome primary resistances observed when each of these treatments is administerd alone.
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