Current progress of immune checkpoint inhibitors in the treatment of advanced hepatocellular carcinoma

Liver cancer is the sixth most common type of malignant tumor and the third leading cause of cancer-associated deaths [1,2]. Hepatocellular carcinoma (HCC) accounts for approximately 75–85% of primary liver cancers and is currently one of the most common malignant tumors, which seriously threatens people’s lives and health. The vast majority of HCC cases occur in the setting of chronic liver disease, with cirrhosis being the primary risk factor for HCC. Currently, surgical treatment is still the main approach to obtain a radical cure for HCC, including early hepatectomy and liver transplantation, with a 5-year survival rate of up to 70% [3]. For patients with advanced HCC, various non-surgical treatments such as transcatheter arterial chemoembolization (TACE), local ablation therapy, radiotherapy, and molecular targeted drug therapy with sorafenib can be selected [4–8]. However, the treatment of advanced HCC is still insufficient and the tumor is prone to invasion, metastasis, and recurrence, resulting in a low overall survival (OS) rate, high mortality, and a poor prognosis.

In recent years, with the rapid development of molecular immunology, tumor immunotherapy has come into being, providing a new option for the treatment of HCC. Tumor immunotherapy refers to the use of the immune defense mechanism of the body to enhance the antitumor immune response and overcome the immune escape of the tumor through various methods, thereby controlling and killing tumor cells. The current progress of tumor immunotherapy manifests itself primarily in the immune checkpoint (ICP) inhibitor (ICI), and is mainly represented by tumor vaccine therapy (dendritic cell [DC] vaccine and oncolytic virus vaccine), and adoptive cell therapy (ACT); among them, ICI therapy is of particular concern and has achieved positive results [9,10]. In September 2017, the U.S. Food and Drug Administration (FDA) approved nivolumab for patients with HCC previously treated with sorafenib, marking the official arrival of the era of immunotherapy for liver cancer.

The mechanisms of tumor immune escape have been intensively explored [11–13]. Tumors can induce and establish a tumor microenvironment (TME) conducive to immunosuppression, including immunosuppressive cells and molecules, resulting in the loss of antitumor function of T cells and triggering immune escape. Regulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs) are the most important components of immunosuppressive cells. Furthermore, immunosuppressive molecules include ICPs, such as the programmed cell death 1 (PD-1) receptor and its ligands programmed death ligand 1 (PD-L1) and PD-L2, as well as the cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) [14]. ICIs, including anti-PD-1, anti-PD-L1, and anti-CTLA-4 antibodies, can enhance the activities of effective T cells and inhibit immunosuppression in the TME [15,16]. Furthermore, lymphocyte activation gene-3 (LAG-3), as an ICP control protein, has its main function in negatively regulating T-cell immunity. It is expected to become the primary target, second only to PD-1 in the development of cancer treatment [17]. T-cell immunoglobulin mucin-3 (TIM-3) was first identified as an immunosuppressive molecule on the surface of T helper 1 (Th1) cells [18], and animal studies involving gene knockout and tumor-bearing mouse models have shown that compared with treatment with anti-CTLA-4 and anti-PD-1 antibodies, the anti-TIM-3 antibody (Ab) does not cause obvious autoimmune side effects, suggesting that it has good prospects for clinical application [19]. The T-cell immunoglobulin and ITIM domain protein (TIGIT) is also a type I transmembrane protein that is expressed mainly in activated T cells, Tregs, memory T cells, and NK cells. TIGIT is usually co-expressed with LAG-3, TIM-3, and PD-1. They jointly participate in the immune recognition of the body and are closely related to patient survival [20]. In summary, ICP offers new hope to patients with advanced HCC [21]. Here, we review the latest research on the mechanism and clinical application of ICIs in the occurrence and development of HCC. New biomarkers for predicting treatment response are described, and the future direction of ICP therapy has been prospected.

The blood supply to the liver comes from portal veins and hepatic arteries. The blood in the portal veins and hepatic arteries contains autoantigens and endogenous antigens, respectively. When a variety of autoantigens and endogenous antigens flow through the liver, autoimmune tolerance is established that prevents the liver from being damaged by the autoimmune reaction [22]. Due to this immune tolerance mechanism, tumor cells in the liver can more easily escape the immunity of the body, avoiding being recognized and killed under the surveillance of the immune system. Furthermore, in the TME, various immunosuppressive cells or molecules form a complex regulatory network to promote tumor cell immune tolerance and escape the body’s immune surveillance (Figure 1). Immunosuppressive cells, such as the increase in Tregs in peripheral blood and tumor-infiltrating lymphocytes (TILs) in patients with liver cancer, can promote transforming growth factor-β (TGF-β) or increase the inhibitory regulatory molecules CTLA4 and PD-L1, further inhibiting the immune response [23,24]. In cancer, myeloid cell differentiation often changes, producing a group of MDSCs to promote angiogenesis and immunosuppression in the TME [25]. Some clinical studies indicate that targeting MDSCs can significantly improve the antitumor effects of sorafenib and ICIs [26]. ICPs, as an important class of immunosuppressive molecules, are expressed on the membrane of different types of immune cells, such as natural killer cells, DCs, tumor-associated macrophages, monocytes, and B and T cells [27]. These ICP proteins function as physiological inhibitors to prevent the activation of these cells, avoiding possible off-target tissue damage. Studies have found that the high expression of ICPs in HCC is related to tumor invasion, progression, and a poorer prognosis. After suppressing ICP expression in HCC models, the in vivo growth of HCC is largely inhibited [28,29], and the high expression of ICPs appears to be the key point for HCC to produce immune tolerance. The ICP CTLA-4 has a high degree of homology to CD28, so it can compete with CD28 for the binding site of the B7 molecule on the antigen-presenting cell (APC) surface, thus exerting the function of inhibiting T cells. In addition, CTLA-4 is also expressed on the Treg cell membrane. It inhibits T-cell activation by enhancing Treg activity and differentiation. Treg s derived from liver cancer can interfere with DC function and down-regulate CD80/CD8 expression on DCs in a cell contact-dependent manner in vitro [30]. Programmed death receptor-1 (PD-1) is a type I transmembrane glycoprotein located on the surface of T cells. It is also expressed on activated B cells and myeloid cells. PD-L1/PD-L2 are PD-1 ligands expressed on a variety of cells. When PD-L1/PD-L2 binds to its receptor, its downstream tyrosine residues are phosphorylated, thus recruiting protein tyrosine phosphates (PTPs), such as SHP2, to dephosphorylate key kinases in downstream pathways, such as ZAP70, P13K-AKT, and RAS-ERK. Currently, several ICI clinical trials conducted in the field of advanced HCC have shown that the objective response rate (ORR) of PD-1/PD-L1 inhibitor monotherapy can reach 10–20%, and is safe and reliable [31]. It was recommended in the treatment guidelines as a second-line treatment for advanced HCC.

HCC usually occurs in the context of liver inflammation, in which PD-1 is highly expressed in intrahepatic lymphocytes, while its ligands, PD-L1 and PD-L2, are highly expressed in Kupffer cells, sinusoidal endothelial cells, and leukocytes once cells are exposed to pro-inflammatory cytokines [32]. PD-1 inhibitors interfere with the binding of PD-1 to PD-L1 and PD-L2 and promote the recognition and killing of tumor cells by the immune system. PD-1 inhibitors have been demonstrated to be effective therapeutics in melanoma, non-small-cell lung cancer (NSCLC), renal cell cancer, bladder cancer, and head and neck squamous cell carcinoma [33]. Nivolumab is the first fully humanized IgG4 monoclonal antibody against PD-1. In 2017, the U.S. FDA approved it for use in patients with advanced HCC who relapsed or became intolerant after sorafenib treatment. In the phase I/II CheckMate040 dose escalation and expansion trial, nivolumab was investigated in 262 patients with unresectable liver cancer (Table 1). The patients included those who were initially treated with sorafenib. The results indicated that the ORR in the dose-expansion group was 20% and the median progression-free survival (PFS) was 4.0 (2.9–5.4) months. In the dose-escalation group, the median OS was 15.6 (13.2–18.9) months. Treatment-related adverse events (AEs) of grade 3–4, including fatigue and diarrhea, occurred in 18 and 23% of the patients in these two groups, respectively, suggesting that the safety of nivolumab is manageable and no new symptoms were observed in patients with advanced HCC [34]. Pembrolizumab is another PD-1 monoclonal antibody. In the KEYNOTE-224 study, 104 patients with advanced HCC who were intolerant to sorafenib or had imaging progression after treatment received pembrolizumab, with an ORR of 17% and a disease control rate (DCR) of 62%, and an mPFS and mOS of 4.9 and 12.9 months, respectively. At the data cut-off date, 17 patients (16%) were still receiving pembrolizumab treatment. Common grade 3 treatment-related events include elevated transaminases and fatigue. Immune hepatitis occurred in 3% of the patients, but there was no viral outbreak [35]. These results indicate that pembrolizumab is effective and tolerable in patients with advanced HCC who had previously been treated with sorafenib. Although pembrolizumab did not reach the established statistical difference, the prolonged trend in OS and PFS suggests that patients can benefit from treatment [36]. Atezolizumab is a new monoclonal antibody that targets the PD-L1 protein. Atezolizumab binds to PD-L1 expressed on tumor cells and tumor-infiltrating immune cells, blocking its interaction with PD-1 and B7.1 receptors. By inhibiting PD-L1, T cells can be activated to destroy tumor cells. In the IMbrave150 experiment, atezolizumab-bevacizumab achieved good results in patients with advanced liver cancer [37]. In addition, camrelizumab, durvalumab, avelumab, and other ICIs have been reported in various experiments, and more first-line treatment options may be developed in the future (Table 1) [34–46].

CTLA-4, the first clinically targeted ICP receptor, is a T lymphocyte surface protein that regulates the amplitude of T-cell activation at the initial stage [47]. CTLA-4 inhibitors (such as ipilimumab and tremelimumab) improve the activity of APC and T lymphocytes to recognize and eliminate tumor cells. An NCT study indicated that after treatment of 20 patients with advanced HCC with tremelimumab, the ORR was 17.6% and the DCR 17.6%, with a median PFS of 6.48 months. A significant drop in viral load was observed when new emerging variants of hypervariable region 1 of hepatitis C virus (HCV) replaced the predominant variants present before therapy. It was assumed that this antiviral effect is associated with an enhanced specific anti-HCV immune response [42]. A multicenter randomized phase III study (NCT04039607) investigating nivolumab in combination with ipilimumab as the first-line treatment was scheduled to be completed in September 2023. The FDA has approved nivolumab plus ipilimumab for the treatment of advanced HCC in patients who were previously treated with sorafenib in 2020 [48]. However, this class of immunotherapy has not been approved as a single-agent therapy in HCC.

PD-1/PD-L1 and CTLA-4 inhibitors can be used alone or in combination with other ICIs to treat malignant tumors. For certain types of solid tumors, combination therapy has a favorable therapeutic effect. For example, when durvalumab (anti-PD-L1 antibody) plus tremelimumab (anti-CTLA-4 antibody) was used to treat primary HCC, ORR increased by 47% compared with durvalumab alone [49]. Since these two antibodies act at different checkpoints, they may have therapeutic synergies. In the CheckMate040 subcohort study, 148 patients who received sorafenib were treated with nivolumab plus ipilimumab. The results suggested that ORR was 31% with increased OS compared with sorafenib alone. Furthermore, the combination of nivolumab plus ipilimumab was determined to have manageable safety, a promising ORR, and a durable response [43]. PD-1 inhibitors alone may not be able to activate a sufficient number of T lymphocytes, and combined use with CTLA-4 inhibitors may further increase the number of activated T lymphocytes, leading to more T lymphocytes in the TME and increased antitumor activity. Therefore, various combination therapies should be further explored to improve therapeutic efficacy.

In recent years, the combination of a variety of molecularly targeted drugs with different mechanisms of action to control the progression of advanced tumors has become a hot topic for researchers. In 2007, sorafenib, a tyrosine kinase inhibitor (TKI), was demonstrated to improve OS in the Sorafenib HCC Assessment Randomized Protocol and Asia-Pacific trials, opening the door for its use in HCC treatment [4]. It has dual antitumor effects. It not only directly inhibits tumor cell proliferation by blocking the RAF/MEK/ERK-mediated signal transduction pathway but also indirectly inhibits tumor cell growth by blocking VEGFR and platelet-derived growth factor (PDGF) receptors, thereby cutting off tumor blood vessel formation. Clinical trials of anti-PD-1 antibodies combined with TKI, including sorafenib (NCT03211416, NCT03439891, NCT02988440), regorafenib (NCT03347292), cabozantinib (NCT03299946 and NCT01658878), and axitinib (NCT03289533), have shown that, compared with monotherapy with TKI, combination therapy could provide more survival benefits in patients with advanced HCC. Bevacizumab is a monoclonal antibody that targets vascular endothelial growth factor (VEGF) and inhibits angiogenesis and tumor growth. The latest data from the phase III clinical study IMbrave150 [37] were announced at the 2019 ESMO-ASIA. OS at 12 months was 67.2% with atezolizumab-bevacizumab and 54.6% with sorafenib. The median PFS was 6.8 and 4.3 months in the respective groups. Grade 3 or 4 AEs occurred in 56.5% of 329 HCC patients who received at least one dose of atezolizumab-bevacizumab and in 55.1% of 156 patients who received at least one dose of sorafenib.

Local regional therapy (LRT) of HCC is an important method for the systemic treatment of advanced liver cancer, including TACE, radiotherapy, and radiofrequency ablation (RFA). Generally, tumors with low mutation loads are less immunogenic and insensitive to ICI treatment. LRT creates conditions for the release of tumor-associated antigens by directly destroying tumor tissues, thus activating tumor antigen phagocytosis mediated by APCs, activating T lymphocytes, and improving sensitivity to ICIs [27].

Radiotherapy is an important treatment for advanced HCC. It promotes immunogenic cell death and releases antigens from irradiated tumor cells, subsequently activating the immune system. At the same time, radiation changes the TME to some extent and alters the immune resistance of tumor cells. Chiang et al. [50] reported that stereotactic body radiotherapy combined with nivolumab for the treatment of unresectable HCC achieved an ORR of 100%. Among the five treated patients, two achieved a complete response and the remaining three achieved a partial response. The median rate for the reduced diameter was 38.7% (30.5–84.5%), the median PFS was 14.9 months, and the 1-year OS and the 1-year local control rate were 100%. A patient had grade 3 toxicities (pneumonitis and skin reaction). There was no classical radiation-induced liver disease. Yu et al. [51] applied radiotherapy during nivolumab treatment in 76 patients and found that patients receiving combined therapy had significantly higher PFS and OS than those receiving nivolumab alone. The results indicated that the combination of chemotherapy with ICIs and radiation therapy is effective for advanced HCC and should be further investigated.

The liver has a dual blood supply from the portal vein and the hepatic artery, and liver cancer is frequently hypervascular. Approximately 90% of the blood supply of the tumor is supplied by the hepatic artery, a blood supply that is much greater in livers with cancer than in normal livers. Based on this characteristic, TACE, a technique that combines intraarterial chemotherapy and selective ischemia, has been used as first-line treatment for patients with intermediate-stage HCC, including those with large or multinodular HCC [5]. TACE is also used to treat patients with unresectable HCC, although long-term survival remains low [52]. Current ongoing trials include the evaluation of the combination of pembrolizumab with TACE for the treatment of advanced HCC (NCT03397654) and nivolumab combined with drug-eluting beads (DEBs)-TACE (NCT03143270) [53], and the results are expected to be announced in the near future.

RFA therapy is currently one of the main interventional treatments for liver cancer. Previous studies have shown that radiofrequency thermal ablation stimulates NK cells, giving them more differentiated and activated phenotypic characteristics, and generally increases their functional activity, improving the antitumor immune response [54]. Duffy et al. [55] reported that tremelimumab in combination with tumor ablation in patients with advanced HCC is feasible and leads to the accumulation of intratumoral CD8+ T cells. Patients were enrolled in this pilot study of tremelimumab at two dose levels (3.5 and 10 mg/kg) and were treated every 4 weeks for a total of six doses, followed by 3 months of infusions until the off-treatment criteria were met. Trimelimumab combined with RFA resulted in partial remission in 26% of HCC patients, resulting in probabilities of PFS at 6 and 12 months of 57.1 and 33.1%, respectively, with a median time to tumor progression (TTP) of 7.4 months (95% CI: 4.7–19.4 months). The median OS was 12.3 months (95% CI: 9.3–15.4 months).

While randomized controlled trials (RCTs) are commonly used to evaluate the safety and efficacy of new drugs, the inclusion and exclusion criteria of RCTs are often too restrictive and the results may not fully conform to the real clinical environment. Real-world research, which aims to generate reliable data on patient responses to drugs in real diagnostic and therapeutic settings, maybe a more appropriate source of data on the safety and efficacy of new drugs. For ICIs, many real-world studies have been performed where large cohorts were analyzed (Table 2) [56–61]. Scheiner et al. [57] conducted an international multicenter real-world cohort study with 65 patients of Child-Pugh class A/B/C (34 nivolumab and 31 pembrolizumab). The results indicated that both inhibitors have promising efficacy and safety in patients with advanced HCC, including subjects with Child-Pugh stage B and patients with intensive pretreatment. Chen et al. [58] found that patients treated with lenvatinib plus ICI had a significantly higher ORR (41.5 vs 20.0%, P=0.023) and DCR (72.3 vs 46.7%, P=0.009) than those treated with lenvatinib. A real-world study by Sung et al. [59] showed that nivolumab treatment seems clinically effective in treating unresectable HCC in an endemic area of HBV infection. Twenty-nine patients (88%) in this cohort were HBsAg positive. These patients were evaluated for efficacy and showed an ORR of 21.4%. The median OS was 26.4 weeks. Liụ et al. [60] also found that the combination of anti-PD-1 immunotherapy plus TKIs proved to be a safe and effective treatment for advanced HCC. Xie et al. [61] included 60 patients treated with sintilimab plus TKI between February 2019 and December 2019, showing an ORR of 36.7% (95% CI: 24.9–48.5%) and a DCR of 81.7% (95% CI: 71.9–91.5%). A total of 46 patients (76.7%) reported AEs, and 8 patients (13.3%) discontinued combination therapy due to grade 3/4 serious AEs.

Studies have indicated that the ORR of ICIs is ∼20% in HCC, which means that a considerable proportion of patients do not respond to this type of treatment. Therefore, appropriate patients should be selected for ICI treatment to achieve a higher ORR. If the population likely to benefit can be screened using predictive biomarkers, the advantages of ICI treatment can be better exploited. The tumor mutation burden (TMB) is an index of the total number of mutations in each coding region of the tumor genome. Theoretically, tumors with higher TMB levels can express more neoantigens, thus eliciting a stronger antitumor immune response and may be targeted for immunotherapy. A high TMB and neoantigen load can predict the response of tumors such as melanoma and NSCLC to anti-PD-1 treatment [62]. Unfortunately, this is not the case in HCC. TMB testing on 755 patients with HCC, of which 74% of patients had TMB of <4 mutations/Mb, and 95% of patients had TMB <10 mutations/Mb, suggested that TMB in HCC was at a low level [63]. Microsatellite instability (MSI) is a hypermutation phenotype caused by mismatch repair defects (dMMRs). In 2017, the FDA approved pembrolizumab for use in patients with advanced or metastatic solid tumors with MSI-H or dMMR. However, MSI in HCC seems to be a rare event [64]. Therefore, the search for markers that predict the response of HCC to immunotherapy still needs further exploration.

PD-L1 expression is the first predictive biomarker in cancer immunotherapy [65]. Sangro et al. observed complete or partial tumor responses in both PD-L1-positive and PD-L1-negative patients treated with nivolumab monotherapy. The median OS of patients with high and low expression of PD-L1 was 28.1 (95% CI: 18.2–N.A) vs. 16.6 months (95% CI: 14.2–20.2), respectively [66]. However, the expression of PD-L1 is controversial in predicting the response to immunotherapy in HCC. Shrestha et al. [33] reported that only 65 of 751 HCC patients expressed PD-L1. Therefore, whether PD-L1 expression can be used to predict the efficacy of ICI in patients with HCC still needs further research.

TILs, including B cells, natural killer cells, and T cells, are an important part of body antitumor immunity. Studies have shown that TILs (especially CD8+ T cells) can be used as a predictor of primary resected liver tumors and as an independent indicator of survival and recurrence of metastatic liver tumors [67]. Katz et al. [68] demonstrated that for metastatic liver tumors, high levels of Treg infiltration had a suppressive effect on immunity. β-catenin is a multifunctional protein encoded by the CTNNB1 gene, and mutations in β-catenin induced activation of WNT signaling and were associated with poor immune cell infiltration [69]. It has been suggested that there are two modes of lymphocyte infiltration in HCC. One type is noninfiltrating, characterized by tumors with mutations in TP53 and CTNNB1 genes, which are insensitive to immunotherapy, and are known as ‘cold tumors’. In contrast, lymphocyte-infiltrating tumors that do not have TP53 or CTNNB1 mutations and are also known as ‘hot tumors’ [70]. Harding et al. [71] analyzed the correlation between therapeutic response and the genome mutation spectrum of 27 HCC patients treated with ICIs and found that activating mutations in the WNT/β-catenin pathway were associated with lower DCR, shorter PFS, and shorter OS. Cellular diversity in tumors is a key factor in therapeutic failures and lethal outcomes of solid malignancies. Sangro et al. [66] found that the four inflammatory gene signature was associated with an improved ORR. Ma et al. [72] found that tumors with higher transcriptomic diversity were associated with worse OS.

Host-related markers and liquid biopsy biomarkers are also recent research hotspots. ESMO demonstrated the predictive value of the neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) in the treatment of liver cancer with nivolumab [73]. Zheng et al. reported that fecal samples from patients who responded to ICI (n=3) during anti-PD-1 immunotherapy for HCC showed a higher Lactobacillus content in their intestinal microbiota than those who did not (n=5). The intestinal microbiota was suggested for the first time to influence the efficacy of PD-1/PD-L1 in the treatment of HCC [74]. Imaging methods have also been used to evaluate the response of advanced HCC to immunotherapy. For example, Qayyum et al. [75] used magnetic resonance elastography (MRE) to evaluate the therapeutic effect of immunotherapy in advanced HCC. In this prospective study, they found that early changes in tumor stiffness in MRE may be an important factor in evaluating the efficacy of treatment for advanced HCC. Age was also a predictor of the ICI response. Studies have shown that the ORR of patients under 65 years of age for anti-PD-1 treatment is low [76]. The reason may be that elderly patients have a less active immune system and anti-PD-1/PD-L1 antibodies can restore lost antitumor immunity, so elderly patients may benefit more. With the deepening of research, an increasing number of prognostic biomarkers related to ICIs have been proposed (Table 3) [33–35,46,63,64,66–68,77–81].

Cancer progression has been reported to be accelerated by an unexpected increase in the progression rate and tumor volume during immunotherapy, often leading to a significant reduction in survival time. This condition is therefore termed hyperprogressive disease (HPD). A more comprehensive definition is as follows: in immunotherapy, the time for tumor progression is less than 2 months, the tumor burden increases by more than 50% compared with the baseline period, and the tumor growth rate (TGR) after immunotherapy increases more than two-fold. The tumor flare caused by treatment is a paradoxical phenomenon and is a significant challenge for the management of immunotherapy in clinics. The reported incidence of HPD is between 4 and 29%, which may depend on the enrolled population and the type of tumor [82–84]. Although HPD frequently occurs in the context of ICB treatment, the mechanism of its occurrence has not been reasonably explained [85]. It is necessary to improve the understanding of the nature of this phenomenon in the clinic to accurately identify suitable patients for immunotherapy. Many studies have been conducted to identify clinical or molecular factors that can be used to predict HPD, such as hemoglobin, Child-Pugh Score, portal vein tumor thrombus (PVTT), NLR, MDM2, BIRC5, circulating tumor DNA (ctDNA), MMR etc. (Table 4) [86–99], although these factors require further validation in HCC and other cancers.

Current studies have demonstrated that ICIs represented by anti-PD-1/PD-L1 and anti-CTLA-4 antibodies have shown good results in the clinical treatment of advanced HCC. ICI combination therapy with LRT or molecularly targeted drugs, such as TKIs, can further improve anticancer efficiency. How to effectively utilize the synergistic effects of different antitumor mechanisms will be the focus of future research and is expected to change the status of HCC treatment. In general, ICIs are safe and cause fewer AEs, such as skin reactions, immune diarrhea, liver and kidney toxicity, immune-related pneumonia, and gastrointestinal disorders. At the same time, the treatment process should be closely monitored, timely detection and treatment of adverse reactions should be performed, and unnecessary treatment interruptions should be reduced. Although ICIs have broad prospects for the treatment of HCC, their ORR is still relatively low. The discovery and application of biomarkers for the effect of ICB therapy will help clinicians effectively screen patients who would benefit from ICI treatment and make individualized treatment more precise. However, at present, biomarkers for ICI beneficiaries of liver cancer are still in the exploratory stage or lack strong evidence, and the combination of multiple biomarkers may be a new development trend. In the future, there is a need to develop more immunosuppressive agents, explore new therapies, and discover new prognostic biomarkers to achieve better treatment results. More RCTs with larger sample sizes are required to further validate the therapeutic results of ICIs for advanced HCC.

The authors declare that there are no competing interests associated with the manuscript.

This work was supported by the National Natural Science Foundation of China [grant number 81872276]; and the Foundation of Anhui Province Key Laboratory of Medical Physics and Technology [grant number LMPT201908].

W.Y. was responsible for the project conception, design, and text editing. X.Y. and T.W. collected materials for the manuscript, analyzed, and wrote relevant content. Y.L. was responsible for editing references and participating in text editing. All authors read and approved the final manuscript.

We thank Professor Meng Xiangling from Anhui Medical University for his constructive discussion and suggestions on the manuscript.

Ab

antibody

ADR

adverse reaction

AE

adverse event

APC

antigen-presenting cell

CTLA-4

cytotoxic T lymphocyte-associated antigen 4

DC

dendritic cell

DCR

disease control rate

dMMR

mismatch repair defect

ESMO

European Society of Medical Oncology

FDA

Food and Drug Administration

HBsAg

hepatitis B surface antigen

HCC

hepatocellular carcinoma

HCV

hepatitis C virus

HPD

hyperprogressive disease

ICB

immune checkpoint blockade

ICI

immune checkpoint inhibitor

ICP

immune checkpoint

LAG-3

lymphocyte activation gene-3

LRT

local regional therapy

MDSC

myeloid-derived suppressor cell

mOS

median overall survival

mPFS

median progression-free survival

MRE

magnetic resonance elastography

MSI

microsatellite instability

NLR

neutrophil-to-lymphocyte ratio

NSCLC

non-small-cell lung cancer

ORR

objective response rate

OS

overall survival

PD-1

programmed cell death 1

PD-L1

programmed death ligand 1

PFS

progression-free survival

RCT

randomized controlled trial

RFA

radiofrequency ablation

TACE

transcatheter arterial chemoembolization

TIGIT

T-cell immunoglobulin and ITIM domain protein

TIL

tumor-infiltrating lymphocyte

TIM-3

T-cell immunoglobulin mucin-3

TKI

tyrosine kinase inhibitor

TMB

tumor mutation burden

TME

tumor microenvironment

Treg

regulatory T cell