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Page 6 of 9                                                  Tang et al. Hepatoma Res 2019;5:19  I  http://dx.doi.org/10.20517/2394-5079.2019.07


            Prior antitumor   therapy  Any (57%)  Surgical resection   (5%)  RFA (19%)  TACE (33%)  Radioembolization   (29%)  Sorafenib (24%)  Sorafenib (22%)  Other systemic   therapies (32%)  TACE (39%)  Resection (28%)  Ablation (28%)  Surgical resection   (60%)  Radiotherapy   (19%)  TACE (55%)  Systemic therapy   (74%)  Sorafenib  (68%)  Surgical resection   (27.3%)  Radiotherapy   (9.1%)  TACE (100%)  sorafenib (54.5%)  Any (95%)  Biologic (38%)  Chemotherapy   (83





            BCLC   stage  A   (14%)  B   (29%)  C   (57%)  B   (25%)  C   (75%)  NG  B   (24%)  C   (76%)  NG  B   (36%)  C   (64%)  NG  NG


            Alpha-  fetoprotein  AFP ≥ 400   ng/mL   (29%)  NG  AFP >200   ng/mL   (41%)  AFP ≥ 400   ng/mL   (37%)  AFP ≥ 400   ng/mL   (46%)  NG  NG



           Child-  Pugh   stage  A   (57%)  B   (43%)  NG  A   (94%)  B (6%)  NG  NG  NG             A   (93%)

           Child-  Pugh   score  6.5   (100%)  5 (44%)  6 (16%)  7 (9%)  NG  5 (70%)  6 (29%)  7-9   (2%)  NG  NG  NG


            ECOG  0   (71.4%)  1   (28.6%)  0 (25%)  1 (75%)  0 (61%)  1 (39%)  NG  0   (81.8%)  1   (18.2%)  0   (42.5%)  1   (57.5%)  NG


            Viral   status     HBV (16%)  HCV (59%)  HBV (21%)  HCV (25%)  HBV (83%)  HCV (23%)  uninfected   HBV (25%)  uninfected   HCV (23%)  uninfected
                HCV  (100%)                              (53%)    HBV   (100%)  HCV   (20%)  (55%)    HBV   (28%)  (50%)
           Age in   year   (range)  65.2   (48-79)  61   (36-76)  68   (62-73)  64   (56-70)  54.8   (42-70)  61.5   (20-77)  NG


            Patient   number  21  32      104      214            11         40                      40


            Duration   of dosing  360 days  6 months  2 years  Depend   on disease   progression  6 cycles  12 months  8 months AFP: alpha fetoprotein; BCLC: barcelona clinic liver cancer; CTLA-4: cytotoxic T-lymphocyte associated antigen 4; ECOG: the eastern cooperative oncology group; PD1: programmed death 1; PD-L1: programmed



            Dosage  15 mg/kg   3.5 mg/kg;   10 mg/kg  200 mg   intravenous   injection  3 mg/kg  4 mg/kg  10 mg/kg   Q2W   NG



            Male,   n (%)  15   (71.4%)  28   (87.5%)  86 (3%)  171   (80%)  8   (72.7%)  32   (80.0%)  NG


                Tremelimumab   Tremelimumab        Nivolumab      Nivolumab  Durvalumab              Durvalumab/  tremelimumab death ligand 1; HCV: hepatitis C virus; HBV: hepatitis B virus; NG: not given; RFA: radiofrequency ablation; TACE: transcatheter arterial embolization
            Agent                         Pembrolizumab



            Target  CTLA-4     CTLA-4     PD-1     PD-1           PD-1        PD-L1                  PD-1   and   CTLA4


       Table 1. Characteristics of patients in included studies
            Race                          White (81%)  Asian (13%)  Black (3%)  Other (2%)  Unknown (1%)  white (49%)  Asian (47%)  Black (3%)  Other 2 (1%)  Asian (100%)  Asian (26.5%)  American   Hawaiian or   other Pacific   Other (2.9%)
                NG             NG                                            White   (55.9%)  Black or   African   (8.8%)  Native   Islander   (5.9%)  NG
            Area  Multi-  center  Multi-  center  Multi-  center  Multi-  center  China  center      Multi-  center

           Clinical   trial   phase  Phase 2  Phase 1  Phase2   Phase1/2  NG  Phase1/2  Multi-       Phase 1


            Year  2013         2017       2018     2017           2017       2017                    2017



            Author  Sangro et al. [15]  Duffy et al. [16]  Zhu et al. [17]  El-Khoueiry et al. [18]  Feng et al. [19]  Wainberg et al. [20]  Kelley et al. [21]



            No  1              2          3        4              5          6                       7
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