ArticleHuman vaccines & immunotherapeutics2026
Cost-effectiveness analysis of sugemalimab plus chemotherapy for the first-line treatment of advanced gastric cancer or gastroesophageal junction cancer.
Article in Human vaccines & immunotherapeutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Camrelizumab plus CAPOX versus CAPOX for HER2-negative gastric or gastro-oesophageal junction adenocarcinoma: a cost-effectiveness analysis.Frontiers in pharmacology · 2026Article
Corrections and comments
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The GEMSTONE-303 trial demonstrated the significant efficacy and safety of sugemalimab plus chemotherapy (S + C) as first-line treatment for patients with advanced gastric cancer (GC) or gastroesophageal junction cancer (GEJC). To evaluate the cost-effectiveness of S + C for advanced GC/GEJC from the perspective of the Chinese healthcare system. A partitioned survival model with a 3-week cycle was created to evaluate the cost-effectiveness of S + C compared to placebo plus chemotherapy (P + C) as the first-line treatment for advanced GC/GEJC. Total costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICERs) as the primary outputs. Sensitivity analyses were performed to evaluate the uncertainty and stability of model parameters. Additionally, subgroup and scenario analyses were conducted. The base-case analysis revealed that the total costs of S + C ($89,510.52) was $49,907.43 higher than that P + C ($39,603.10). However, it also increased the QALYs by 0.29 (1.27 QALYs vs. 0.98 QALYs), with an ICER of $170,440.21/QALY, which was higher than the willingness-to-pay of $40,334.05/QALY. Sensitivity analyses demonstrated that the cost of sugemalimab, utility of progression-free survival and the discount rate had a greater impact on the model. Subgroup analyses indicated that S + C was more cost-effective in patients with advanced GC/GEJC with programmed cell death ligand 1 combined positive score ≥10. Compared to P + C, S + C is currently not an economically viable option for first-line treatment of advanced GC/GEJC in China.
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Registered trials
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