Evidence map›Paper›PMID 42723778›Full record

ArticleFrontiers in public health2026

Cost-effectiveness of tremelimumab plus durvalumab versus sorafenib for unresectable hepatocellular carcinoma in China: an economic evaluation based on five-year overall survival data from the HIMALAYA trial.

Rui Feng, Ping Liang, Yajing Wang, Dong Li, Huixian Jia, Ying Zheng, Liman Huo, Qi Lv

Abstract read
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Article in Frontiers in public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Rui Feng *School of Disaster and Emergency Medicine, Tianjin University, Tianjin, China.
Ping Liang *Department of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Yajing WangDepartment of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Dong LiDepartment of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Huixian JiaDepartment of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Ying ZhengDepartment of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Liman Huo *Department of Pharmacy, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Qi Lv *School of Disaster and Emergency Medicine, Tianjin University, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To assess the cost-effectiveness of tremelimumab plus durvalumab [the Single Tremelimumab Regular Interval Durvalumab (STRIDE) regimen] versus sorafenib as first-line treatment for unresectable hepatocellular carcinoma in China using 5-year follow-up data from the HIMALAYA trial. Methods: A three-state partitioned survival model comprising progression-free survival, progressed disease, and death was developed from the perspective of the Chinese healthcare system. Individual patient data were reconstructed from the published Kaplan-Meier curves from the HIMALAYA trial and used to estimate and extrapolate progression-free and overall survival. The model used 28-day cycles, a 10-year base-case time horizon, and an annual discount rate of 4.5%. Only direct medical costs were included and expressed in 2025 United States dollars. The willingness-to-pay threshold was 27,906 USD per quality-adjusted life-year (QALY). One-way sensitivity analysis, probabilistic sensitivity analysis, and scenario analyses were performed. Results: In the base-case analysis, the STRIDE regimen and sorafenib yielded 1.6937 and 1.2900 QALYs at total costs of 93,507.00 and 8,081.94 USD, respectively. The STRIDE regimen provided an additional 0.4037 QALYs at an incremental cost of 85,425.06 USD, resulting in an incremental cost-effectiveness ratio (ICER) of 211,596.11 USD/QALY. The cost of durvalumab was the principal driver of the ICER. At the prespecified willingness-to-pay threshold, the probability that STRIDE was cost-effective was 0.0%. The ICER remained above the threshold in the durvalumab patient assistance program, 15-year time-horizon, alternative overall survival extrapolation, mixture-cure, and lower progressed-disease utility scenarios. The price of durvalumab would need to decrease by 92.34% for the ICER to reach the prespecified threshold. In contrast, reducing the price of tremelimumab to zero was insufficient to lower the ICER to the threshold when the price of durvalumab remained unchanged. Conclusion: Although the STRIDE regimen improved health outcomes compared with sorafenib, it was not cost-effective at current prices in China. The findings suggest that its clinical value has not yet been matched by its economic value, primarily because of the high cumulative cost of durvalumab maintenance therapy. Future pricing, reimbursement, and patient assistance strategies should focus on reducing the cost of maintenance treatment to improve the value for money of the STRIDE regimen.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularLiver NeoplasmsSorafenibChinaCost-Benefit AnalysisCost-Effectiveness AnalysisFemaleHumansMaleMiddle AgedQuality-Adjusted Life YearsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicaldurvalumabSorafenibtremelimumabcost-effectiveness analysisdurvalumabhealth technology assessmentpartitioned survival modeltremelimumabunresectable hepatocellular carcinoma

Identifiers

PMID42723778
PMCPMC13557980

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.