Cost-effectiveness analysis of anlotinib plus penpulimab versus sorafenib in the treatment of unresectable hepatocellular carcinoma.
Jiefeng Luo, Zhengxiong Li, Chengxia Gui, Qiong Du, Jiyong Liu
Abstract
Open AccessThe APOLLO trial demonstrated that anlotinib plus penpulimab significantly prolonged progression-free survival (PFS) and overall survival compared to sorafenib in patients with unresectable hepatocellular carcinoma (HCC). However, its cost-effectiveness remains uncertain. This study aimed to evaluate the cost-effectiveness of this regimen from the perspective of the Chinese healthcare system. We constructed a partitioned survival model comprising three health states to evaluate the cost-effectiveness of anlotinib plus penpulimab versus sorafenib for unresectable HCC. Over a 10-y time horizon, we compared the total costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs) between two groups. The robustness of the results was validated through one-way sensitivity analysis and probabilistic sensitivity analysis (PSA). Compared to sorafenib, anlotinib plus penpulimab provided an additional 0.21 QALYs at an incremental cost of $18,194.86. This resulted in an ICER of $86,546.80/QALY. One-way sensitivity analysis revealed that the utility value for PFS exerted the greatest influence on the model results, followed by penpulimab prices and the disutility due to adverse events (grade ≥3) in the anlotinib plus penpulimab group. PSA indicated a 0% probability of the anlotinib plus penpulimab regimen being cost-effective at a willingness-to-pay threshold of $40,335/QALY. Scenario analysis results showed that the Patient Assistance Program of penpulimab could help the regimen achieve favorable cost-effectiveness. Compared with sorafenib, anlotinib plus penpulimab for unresectable HCC patients was unlikely cost-effective under the perspective of the Chinese healthcare system.