# Cost-effectiveness analysis of tislelizumab plus chemotherapy as first-line treatment for HER2-negative advanced gastric or gastro-oesophageal junction adenocarcinoma

**Authors:** Liangliang Zou, Guilan Guo, Yufan Huang, Cuihua Yuan

PMC · DOI: 10.3389/fphar.2025.1500729 · Frontiers in Pharmacology · 2025-05-22

## TL;DR

Adding tislelizumab to chemotherapy improves patient outcomes but is not cost-effective in China for treating advanced stomach cancer.

## Contribution

This study evaluates the cost-effectiveness of tislelizumab plus chemotherapy in China using a Markov model and real clinical trial data.

## Key findings

- Tislelizumab plus chemotherapy provided 1.53 QALYs at $23,484.39 compared to 1.14 QALYs at $12,123.52 for chemotherapy alone.
- The incremental cost-effectiveness ratio was $29,608.51 per QALY gained, exceeding China's willingness-to-pay threshold.
- Tislelizumab plus chemotherapy had only a 0.8% probability of being cost-effective at the threshold of $19,067 per QALY.

## Abstract

The RATIONALE-305 trial indicates that tislelizumab plus chemotherapy (TLE-CHM) offers clinical benefits over placebo plus chemotherapy (PLB-CHM) as a first-line treatment for patients with HER2-negative advanced gastric or gastro-oesophageal junction (G/GEJ) adenocarcinoma. Nonetheless, incorporating tislelizumab results in higher treatment costs, raising concerns about its cost-effectiveness relative to PLB-CHM. This study aimed to assess the cost-effectiveness of TLE-CHM as an initial treatment for HER2-negative advanced G/GEJ adenocarcinoma from the perspective of the Chinese healthcare system.

A Markov partitioned survival model incorporating three health states was developed to evaluate the cost-effectiveness of TLE-CHM as a first-line treatment for advanced G/GEJ adenocarcinoma. Clinical data were sourced from the RATIONALE-305 trial, with drug costs calculated at the national tender price, and additional costs and utility values derived from published literature. The outcomes measured included total costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs). Sensitivity analyses were conducted to validate the model’s robustness.

TLE-CHM achieved 1.53 QALYs at a cost of $23,484.39, compared to 1.14 QALYs at $12,123.52 for PLB-CHM. The ICER for TLE-CHM versus PLB-CHM was $29,608.51 per QALY gained. Key parameters influencing the model results included PFS utility, the cost of tislelizumab, and disease progression utility. At a willingness-to-pay threshold of $19,067 per QALY, TLE-CHM had an 0.8% probability of being cost-effective compared to PLB-CHM.

From the perspective of the Chinese healthcare system, TLE-CHM is not a cost-effective first-line treatment for advanced G/GEJ adenocarcinoma compared to chemotherapy.

## Linked entities

- **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}
- **Diseases:** PLB-CHM (MESH:D000084202), CHM (MESH:D015794), G/GEJ adenocarcinoma (MESH:D005764)
- **Chemicals:** tislelizumab (MESH:C000707970)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC12137247/full.md

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Source: https://tomesphere.com/paper/PMC12137247