Immune-Based Combination Therapies for Advanced Hepatocellular Carcinoma

被引:10
作者
Carloni, Riccardo [1 ,2 ]
Sabbioni, Simone [1 ,2 ]
Rizzo, Alessandro [3 ,6 ]
Ricci, Angela Dalia [4 ]
Palloni, Andrea [1 ,2 ]
Petrarota, Cataldo [3 ]
Cusmai, Antonio [3 ]
Tavolari, Simona [1 ,2 ]
Gadaleta-Caldarola, Gennaro [5 ]
Brandi, Giovanni [1 ,2 ]
机构
[1] Univ Bologna, Dept Specialized Expt & Diagnost Med, Bologna, Italy
[2] IRCCS Azienda Osped Univ Bologna, Div Med Oncol, Bologna, Italy
[3] IRCCS Ist Tumori Giovanni Paolo II, Struttura Semplice Dipartimentale Oncol Med Presa, Bari, Italy
[4] Saverio Bellis Res Hosp, Natl Inst Gastroenterol, Med Oncol Unit, Bari, Italy
[5] Osped Mons AR Dimiccoli, Unita Operativa Complessa Oncol Med, Barletta, Italy
[6] IRCCS Ist Tumori Giovanni Paolo II, Struttura Semplice Dipartimentale Oncol Med Presa, Viale Orazio Flacco 65, I-70124 Bari, Italy
关键词
hepatocellular carcinoma; VEGF; PD-1; tislelizumab; atezolizumab; durvalumab; ATEZOLIZUMAB PLUS BEVACIZUMAB; INFILTRATING T-CELLS; PHASE-I TRIAL; CHILD-PUGH; OPEN-LABEL; SAFETY; SORAFENIB; LANDSCAPE; NIVOLUMAB; VACCINE;
D O I
10.2147/JHC.S390963
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) is the fourth most frequent cause of cancer-related death worldwide. HCC frequently presents as advanced disease at diagnosis, and disease relapse following radical surgery is frequent. In recent years, immune checkpoint inhibitors (ICIs) have revolutionized the treatment of advanced HCC, particularly with the introduction of atezolizumab/ bevacizumab as the new standard of care for first-line treatment. Recently, dual immune checkpoint blockade with durvalumab plus tremelimumab has also emerged as an effective first-line treatment for advanced HCC and most of the research is currently focused on developing combination treatments based mainly on ICIs. In this review, we will discuss the rationale and ongoing clinical trials of immune-based combination therapies for the treatment of advanced HCC, also focusing on new immunotherapy strategies such as chimeric antigen receptor T cells (CAR-T) and anti-cancer vaccines.
引用
收藏
页码:1445 / 1463
页数:19
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