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. 2022 Jan 27;14(1):140–157. doi: 10.4254/wjh.v14.i1.140

Table 1.

Immune checkpoint inhibitor therapy for hepatocellular carcinoma

Immune checkpoint inhibitor therapy
Agent
Type of study
Study details
Outcome
Tremelimumab (anti-CTLA4)[45] Phase II clinical trial 21 HCC patients infected with hepatitis C virus and not eligible for surgery or locoregional therapy 15 mg/kg IV every 90 d 17.6% patients-partial response; 58.8% patients-stable disease; Time to progression-6.48 mo; Overall survival-8.2 mo; Decreased viral load
TRC105 (carotuximab) antibody to CD105[46] Phase I/II study TRC105 (15 mg/kg) every 2 wk given with sorafenib 400 mg twice daily Tumor ablation utilizing RFA and TACE enhance the efficacy of tremelimumab; Improves intratumoral effector CD8+ T cells infiltration
Nivolumab (anti-PD-1)[47] CheckMate 040 phase I/II dose-escalation study 182 patients with advanced HCC; Patients naive to or previously treated with sorafenib received 0.1-10 mg/kg and 3 mg/kg once every 2 wk Durable responses with long-term survival and favorable safety in both sorafenib-naive and -experienced patients; 3.8% complete response, 14.8% partial response, and 62.6% disease control rate
Nivolumab (anti-PD-1)[33] Phase I/II study NCT01658878 262 HCC patients; HCC patients on sorafenib 1.4% complete response; 18.2% partial response; 83% overall survival at 6 mo
Pembrolizumab (anti-PD-1)[48] KEYNOTE-224 trial 104 advanced HCC patients on sorafenib 1% complete response; 16% partial response; 54% overall survival at 12 mo
Durvalumab (PD-L1) and tremelimumab (CTLA4)[49] Phase I/II, open-label, randomized study For the efficacy of durvalumab combined with tremelimumab in unresectable HCC No unexpected safety signals with durvalumab and tremelimumab seen in unresectable HCC patients
Tremelimumab (CTLA4)[50] Phase II trial NCT01853618 32 patients with HCC with HCV; Tremelimumab at 3.5 and 10 mg/kg i.v. every 4 wk for 6 doses, followed by 3-monthly infusions; Combined with subtotal radiofrequency ablation or chemoablation at day 36 No dose-limiting toxicities; Accumulation of intratumoral CD8+ T cells; 26% partial response

CTLA-4: Cytotoxic T lymphocyte protein 4; PD-1: Programmed cell death protein 1; HCC: Hepatocellular carcinoma; HCV: Hepatitis C virus; RFA: Radiofrequency ablation; TACE: Transarterial chemoembolization.