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Wu et al. Hepatoma Res 2023;9:6  https://dx.doi.org/10.20517/2394-5079.2022.37  Page 11 of 15

               Table 1. Ongoing clinical trials
                Study Title              Aim                               Interventions    Locations
                TACE, Sorafenib and PD-1 Monoclonal  Prospective study assessing objective response rate   ● Combination Product:   Sichuan Cancer
                Antibody in the Treatment of HCC   and overall survival as primary outcomes  TACE combined with   Hospital and
                (NCT04518852)                                              sorafenib and PD-1 mAb  Research Institute,
                                                                                            China
                DEB-TACE Plus Lenvatinib or Sorafenib  This is a prospective study aiming to investigate the   ● Drug: DEB-TACE plus   Guangxi Medical
                or PD-1 Inhibitor for Unresectable   safety and efficacy of DEB-TACE plus sorafenib or   Sorafenib   University Cancer
                Hepatocellular Carcinoma   lenvatinib or PD-1 Inhibitor for unresectable HCC.  ● Drug: DEB-TACE plus   Hospital, China
                (NCT04229355)                                              Lenvatinib
                                                                           ● Drug: DEB-TACE plus
                                                                           PD-1 inhibitor
                A Novel Immunotherapy PD-1 Antibody  The use of novel immunotherapy using the PD-1   ● Drug: PD-1 antibody   Affiliated Tumor
                to Suppress Recurrence of HCC   antibody could suppress postoperative recurrence   ● Procedure: TACE  Hospital of Guangxi
                Combined With PVTT After Hepatic   and prolong HCC patients survival period effectively.  Medical University,
                Resection                                                                   China
                (NCT03914352)
                IMMULAB - Immunotherapy With                               ● Drug: Pembrolizumab   Hannover Medical
                Pembrolizumab in Combination With                          ● Procedure: Radio   School, Germany
                Local Ablation in Hepatocellular                           Frequency Ablation (RFA)
                Carcinoma (HCC)                                            ● Procedure: Microwave
                (NCT03753659)                                              Ablation (MWA)
                Autologous Immune Cell Therapy in   To assess the safety of Autologous Immune Cell   ● Biological: DC-TC +   Shanghai, China
                Primary Hepatocellular Carcinoma   Therapy in Primary Hepatocellular Carcinoma   GM-CSF
                Patients Following Resection and TACE  Patients Following Resection and TACE Therapy
                Therapy
                (NCT01828762)
                Tremelimumab With        To assess the safety and feasibility of combining   ● Drug: Tremelimumab   National Institutes of
                Chemoembolization or Ablation for   Tremelimumab with trans-arterial catheter   ● Procedures: RFA, TACE  Health Clinical
                Liver Cancer             chemoembolization (TACE) radiofrequency ablation  and cryoablation  Center, Maryland,
                (NCT01853618)            (RFA) or cryoablation in patients with advanced HCC  USA



               improved efficacy with TACE and sorafenib, which highlights the importance of timing the administration
               of therapy and evaluation of tumor progression. Further studies may adopt the methods used in the
               TACTICS trial to determine if there is a further significant improvement. Combining LRT and
               immunotherapy  works  to  create  a  synergistic  boost  in  the  existing  immune  response.  Given
               immunotherapy in HCC is relatively new, the combination of these agents with LRT is up and coming as
               multiple studies are currently underway. Combined therapy is a promising direction in the treatment for
               HCC and future studies are encouraged to reveal the patient population who will best benefit from these
               therapies.

               DECLARATIONS
               Author contribution
               Contributed to the conception and the design of the study, data search and manuscript writing: Wu Y
               Made contributions to conception, manuscript writing, and table design: Wakil A
               Performed data acquisition and manuscript writing: Solomon F
               Supervised the article concept and manuscript review: Pyrsolpoulos N


               Availability of Data and Materials
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               Financial support and sponsorship
               None.
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