# Cost-effectiveness of ramucirumab plus paclitaxel as maintenance therapy for patients with advanced HER2-negative gastric or gastroesophageal junction cancer

**Authors:** Dong Li, Xue Zhao, Huixian Jia, Rong Cui, Afang Cao, Liman Huo

PMC · DOI: 10.3389/fonc.2026.1713870 · Frontiers in Oncology · 2026-02-09

## TL;DR

This study evaluates whether adding ramucirumab to paclitaxel is a cost-effective treatment for advanced stomach cancer in China, finding it is not currently cost-effective without significant price reductions.

## Contribution

The study introduces a cost-effectiveness analysis of ramucirumab plus paclitaxel as maintenance therapy for gastric cancer in the Chinese healthcare context.

## Key findings

- At current pricing, ramucirumab plus paclitaxel is not cost-effective in China.
- Price reductions of up to 24% are needed for cost-effectiveness.
- Even with a patient assistance program, further price cuts are required.

## Abstract

This study a to evaluate the cost-effectiveness of ramucirumab plus paclitaxel as a switch maintenance therapy for patients with advanced HER2-negative gastric or gastroesophageal junction cancer, from the perspective of the Chinese healthcare system, to guide clinical decision-making and reimbursement policies.

A three-state Markov model (progression-free, progressed disease, and death) was developed based on data from the ARMANI phase III randomized controlled trial. Two treatment strategies were compared: ramucirumab plus paclitaxel versus continuation of oxaliplatin-based chemotherapy (FOLFOX/CAPOX). Cost data were obtained from national procurement platforms and published literature; utility values were derived from EQ-5D instruments. A willingness-to-pay (WTP) was set at three times China’s 2024 per capita GDP, equivalent to USD 40, 457.32 per QALY.Base-case analysis, one-way and probabilistic sensitivity analyses, threshold price analysis, and a patient assistance program (PAP) scenario were conducted.

The base-case analysis yielded an incremental cost-effectiveness ratio (ICER) of USD 138, 320.14/QALY, which exceeded the WTP threshold. Under the PAP scenario (i.e., “buy two, get one free”), the ICER was reduced to USD 95, 304.89/QALY, but remained above the threshold. Sensitivity analyses showed the model was most sensitive to utility values, discount rates, and drug price. Threshold analysis suggested that the price of ramucirumab would need to be reduced to approximately 24% of its current level (~USD 149/100mg) to achieve cost-effectiveness; even under the PAP scenario, a further price cut to 36% (~USD 223/100 mg) would still be required.

At current pricing and under the existing PAP framework, ramucirumab plus paclitaxel is not a cost-effective switch maintenance strategy in advanced HER2-negative gastric or gastroesophageal junction cancer in China. Significant price reductions through national negotiations may enable this regimen to become economically viable within the Chinese healthcare system.

## Linked entities

- **Chemicals:** paclitaxel (PubChem CID 36314), oxaliplatin (PubChem CID 9887053), FOLFOX (PubChem CID 135659064)
- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, PLAG1 (PLAG1 zinc finger) [NCBI Gene 5324] {aka PSA, SGPA, SRS4, ZNF912}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}
- **Diseases:** Gastric cancer (MESH:D013274), bleeding disorders (MESH:D006470), cachexia (MESH:D002100), wasting (MESH:D019282), cancer (MESH:D009369), height loss (MESH:C000719188), vasculitis (MESH:D014657), fistula (MESH:D005402), Chronic Disease (MESH:D002908), gastrointestinal bleeding (MESH:D006471), gastric cancerand (MESH:D013272), thromboembolic (MESH:D013923), PD (MESH:D018450), peripheral neuropathy (MESH:D010523), gastrointestinal perforation (MESH:D005767), toxicity (MESH:D064420), weight loss (MESH:D015431), anemia (MESH:D000740), hypertension (MESH:D006973), death (MESH:D003643), venous thromboembolism (MESH:D054556), neutropenia (MESH:D009503), Nutrition (MESH:D044342)
- **Chemicals:** Oxaliplatin (MESH:D000077150), aspirin (MESH:D001241), 5-fluorouracil (MESH:D005472), leucovorin (MESH:D002955), Paclitaxel (MESH:D017239), Ramucirumab (MESH:C543333), platinum (MESH:D010984), heparin (MESH:D006493), warfarin (MESH:D014859), capecitabine (MESH:D000069287), FOLFOX (MESH:C410216), CAPOX (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12926126/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926126/full.md

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Source: https://tomesphere.com/paper/PMC12926126