Evidence map›Paper›PMID 42539464›Full record

ArticleFrontiers in pharmacology2026

Disitamab vedotin plus toripalimab as a first-line treatment for HER2-expressing advanced urothelial cancer: a cost-effectiveness analysis from China based on the RC48-C016 trial.

Xiaolin Yun, Qiongshi Wu, Chenxin Zeng

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
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

Corrections and comments

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

3 authors.

Xiaolin YunDepartment of Pharmacy, Hainan General Hospital, Haikou, China.
Qiongshi WuDepartment of Pharmacy, Hainan General Hospital, Haikou, China.
Chenxin ZengDepartment of Pharmacy, Jinhua Municipal Central Hospital, Jinhua, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The phase III RC48-C016 trial demonstrated that disitamab vedotin plus toripalimab (DV + T) provides significant survival benefits compared to chemotherapy in patients with HER2-expressing advanced urothelial cancer (UC), along with a favorable safety profile. However, its cost-effectiveness has not yet been evaluated. This study aims to evaluate the cost-effectiveness of DV + T versus chemotherapy as first-line treatment for HER2-expressing advanced UC from the perspective of the Chinese healthcare system. Methods: A partitioned survival model with a 15-year time horizon was developed to evaluate the cost-effectiveness of DV + T compared to chemotherapy. Outcomes included total cost, quality-adjusted life year (QALY), and the incremental cost-effectiveness ratio (ICER). Model uncertainty was examined through one-way and probabilistic sensitivity analyses. Results: DV + T yielded 2.44 QALYs at a total cost of $98,514.95, while chemotherapy yielded 1.43 QALYs at a cost of $28,300.87. The ICER was $69,575.31 per QALY. In China, at a willingness-to-pay (WTP) threshold of $20,167.02 per QALY, DV + T has a 0% probability of being cost-effective as a first-line treatment for HER2-expressing advanced UC compared to chemotherapy. Subgroup analysis suggested that the ICER of DV + T versus chemotherapy tended to be substantially lower in patients ineligible to receive cisplatin ($61,264.33 per QALY) than in those eligible for cisplatin-based chemotherapy ($245,983.12 per QALY). Conclusion: From the perspective of the Chinese healthcare system, DV + T is not cost-effective as first-line treatment for HER2-expressing advanced UC compared to chemotherapy.

Indexed as

advanced urothelial cancerchemotherapycost-effectivenessdisitamab vedotinpartitioned survival modeltoripalimab

Identifiers

PMID42539464
PMCPMC13423685

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