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Camrelizumab plus rivoceranib versus sorafenib as first-line therapy for patients with unresectable hepatocellular carcinoma: a cost–utility analysis in China and the United States

Affiliation
Clinical Oncology School of Fujian Medical University ,Fujian Cancer Hospital ,Fuzhou ,Fujian ,China
Zhao, Qiuling;
Affiliation
School of Pharmacy ,Fujian Medical University ,Fuzhou ,Fujian ,China
He, Yimin;
Affiliation
School of Pharmacy ,Fujian Medical University ,Fuzhou ,Fujian ,China
Nian, Zilin;
Affiliation
School of Pharmacy ,Fujian Medical University ,Fuzhou ,Fujian ,China
Huang, Yongjian;
Affiliation
Clinical Oncology School of Fujian Medical University ,Fujian Cancer Hospital ,Fuzhou ,Fujian ,China
Huang, Ruyi;
Affiliation
Clinical Oncology School of Fujian Medical University ,Fujian Cancer Hospital ,Fuzhou ,Fujian ,China
Lai, Lijun;
Affiliation
Clinical Oncology School of Fujian Medical University ,Fujian Cancer Hospital ,Fuzhou ,Fujian ,China
Yang, Lin

Objective Camrelizumab plus rivoceranib (camr-rivo) has been shown to significantly improve overall survival (OS) in patients with unresectable or advanced hepatocellular carcinoma (HCC) in the CARES-310 trial. However, the cost-utility of this treatment remains unclear. Therefore, this study evaluated the cost–utility of camr-rivo versus sorafenib as a first-line systemic therapy for patients with unresectable or advanced HCC from the perspectives of the Chinese healthcare system and the United States (US) payers. Methods Based on the CARES-310 trial, a partitioned survival model was constructed to estimate economic costs and health outcomes over a 10-year lifetime horizon. Drug costs were obtained from the public database, Red Book, and relevant literature. Health utility values were derived from the literature. One-way and probabilistic sensitivity analyses were performed. The willingness-to-pay (WTP) threshold was $36,627.25/QALY in China and $150,000.00/QALY in the United States. Results Camr-rivo yielded an additional 0.34 quality-adjusted life years (QALY) compared to sorafenib for patients with unresectable or advanced HCC. The incremental costs in China and the United States were $4,762.10 and $92,700.49, respectively, and the incremental cost–utility ratios (ICURs) were $14,174.40/QALY and $272,852.59/QALY, respectively. Sensitivity analyses indicated that the cost of rivoceranib and camrelizumab had the greatest impact on the ICUR in China and the United States. Scenario analyses showed that a price reduction of approximately 30% for camrelizumab and rivoceranib could make camr-rivo a cost-utility option in the United States. Conclusion At the set WTP threshold, camr-rivo is a cost–utility treatment strategy compared to sorafenib as a first-line therapy for patients with unresectable or advanced HCC in China but not in the United States.

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License Holder: Copyright © 2025 Zhao, He, Nian, Huang, Huang, Lai and Yang.

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