# Nivolumab plus ipilimumab versus lenvatinib or sorafenib for US and Chinese patients with unresectable hepatocellular carcinoma: a cost-effectiveness analysis

**Authors:** Qiuji Wu, Yi Qin, Qiu Li

PMC · DOI: 10.3389/fpubh.2025.1726477 · Frontiers in Public Health · 2026-01-12

## TL;DR

This study compares the cost-effectiveness of two cancer treatments in the US and China, finding that the newer combination therapy offers better value for money.

## Contribution

The study provides a comparative cost-effectiveness analysis of immunotherapy versus targeted therapy for hepatocellular carcinoma in the US and China.

## Key findings

- In the US, NIVO + IPI had an ICER of $127,063.87 per QALY, below the $150,000/QALY threshold.
- In China, NIVO + IPI had an ICER of $37,615.40 per QALY, below the $39,933.67/QALY threshold.
- Sensitivity analyses confirmed the cost-effectiveness of NIVO + IPI in both countries.

## Abstract

The CheckMate 9DW trial showed that nivolumab plus ipilimumab (NIVO + IPI) improves overall survival over lenvatinib or sorafenib (LEN/SOR) in patients with unresectable hepatocellular carcinoma (uHCC). We evaluated the cost-effectiveness of NIVO + IPI versus LEN/SOR from payer perspectives in the United States (US) and China, explicitly aiming to inform reimbursement and price-negotiation decisions in each setting.

Based on the overall and subgroup data from the CheckMate 9DW trial, we developed a partitioned survival model to compare the clinical outcomes of NIVO + IPI versus LEN/SOR. Costs included drugs, administration, monitoring, adverse event management, and follow-up care in both the US and China. A lifetime horizon (1-month cycles) and 2024 US dollars were applied. The primary outcome was the incremental cost-effectiveness ratio (ICER), expressed as cost per quality-adjusted life year (QALY) gained. Willingness-to-pay (WTP) thresholds were $150,000/QALY (US) and $39,933.67/QALY (China). Model uncertainty was assessed through one-way and probabilistic sensitivity analyses.

In the US, the NIVO + IPI regimen generated an incremental gain of 0.68 QALYs at an additional cost of $86,403.43, resulting in an ICER of $127,063.87 per QALY. In the China subgroup, NIVO + IPI yielded an incremental gain of 0.94 QALYs with an incremental cost of $35,358.47, corresponding to an ICER of $37,615.40 per QALY. Sensitivity analyses indicated that the ICER was mostly influenced by variations in the discount rate and drug prices. Probabilistic sensitivity analysis demonstrated that the probability of NIVO + IPI being cost-effective exceeded 50% at the respective WTP thresholds in both the United States and China.

This study suggests that NIVO + IPI is cost-effective in both the United States and China at current price levels.

## Linked entities

- **Chemicals:** lenvatinib (PubChem CID 9823820), sorafenib (PubChem CID 216239)
- **Diseases:** hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Diseases:** hepatocellular carcinoma (MESH:D006528)
- **Chemicals:** ipilimumab (MESH:D000074324), lenvatinib (MESH:C531958), IPI (-), sorafenib (MESH:D000077157), NIVO (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12832771/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12832771/full.md

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Source: https://tomesphere.com/paper/PMC12832771