Evidence map›Paper›PMID 42577174›Full record

ArticleFrontiers in public health2026

Cost-effectiveness analysis of sacituzumab tirumotecan vs. chemotherapy for patients with EGFR-TKI-resistant, EGFR-mutated advanced non-small cell lung cancer in China.

Kai Xu, Yuting Yan, Zhaoliu Cao, Jinchun Liu, Hongting Yao, Yuyang Sun, Jingyu Zhang, Hong Wu

Abstract read
In one paragraph

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

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

8 authors.

Kai XuDepartment of Pharmacy, Nanjing Qixia Community Healthcare Center, Nanjing, Jiangsu, China.
Yuting YanShanghai Key Laboratory of Emotions and Affective Disorders, Songjiang District Central Hospital, Songjiang Research Institute, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Zhaoliu CaoDepartment of Pharmacy, Nanjing Qixia District Hospital, Nanjing, Jiangsu, China.
Jinchun LiuDepartment of Pharmacy, Nanjing Drum Tower Hospital, Nanjing, Jiangsu, China.
Hongting YaoDepartment of Pharmaceutical Regulatory Science and Pharmacoeconomics, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Yuyang SunDepartment of Pharmaceutical Regulatory Science and Pharmacoeconomics, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu, China.
Jingyu ZhangDepartment of Oncology, Affiliated Lianyungang Clinical College of Nantong University, Lianyungang, Jiangsu, China.
Hong WuDepartment of Pharmacy, The Second People's Hospital of Lianyungang & The Oncology Hospital of Lianyungang, Lianyungang, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In the OptiTROP-Lung04 trial, sacituzumab tirumotecan (sac-TMT) yielded a median progression-free survival of 8.3 months-a clinically significant outcome that has approval by the National Medical Products Administration. This study evaluates the cost-effectiveness of sac-TMT as a later-line therapy for patients with EGFR-mutant advanced NSCLC who have progressed on EGFR-TKIs, from the perspective of Chinese healthcare system. Methods: A partitioned survival model was constructed to simulate patients' health state transitions in 28-day cycles and predict long-term survival and economic outcomes over a 10-year time horizon for the two treatment strategies. Clinical data were sourced from the OptiTROP-Lung04 trial, whereas cost and utility parameters were extracted from local medical charges and published literatures. The model calculated total costs, life-years (LYs), quality-adjusted life-years (QALYs), and the incremental cost-effectiveness ratio (ICER). One-way and probabilistic sensitivity analyses were conducted to verify the robustness of model outputs. Scenario analyses evaluated changes in the ICER under different sac-TMT price levels and alternative time horizons. Subgroup analyses estimated ICER values corresponding to hazard ratios across distinct subgroups. Results: Compared with the chemotherapy group, sac-TMT incurred an incremental cost of $28,285.28 and generated an additional 0.84 QALYs and 1.74 LYs, yielding an ICER of $33,514.79/QALY. One-way sensitivity analysis revealed that cost of sac-TMT, progression-free survival (PFS) utility value, and discount rate were the three parameters exerting the strongest influence on the ICER. Probabilistic sensitivity analysis indicated that sac-TMT had a 23.90% probability of being cost-effective. Scenario analysis demonstrated that the ICER would precisely hit the cost-effectiveness threshold ($27,906.03/QALY) if the unit price of sac-TMT decreased to $541.55/200 mg. Conclusions: Based on this analytical model, sac-TMT is unlikely to be cost-effective for Chinese patients with EGFR-TKI-resistant, EGFR-mutated advanced NSCLC. Nevertheless, a further price reduction of 14.98% would make it cost-effective.

Indexed as

Antineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsChinaCost-Benefit AnalysisCost-Effectiveness AnalysisDrug Resistance, NeoplasmErbB ReceptorsFemaleHumansMaleMutationProtein Kinase InhibitorsQuality-Adjusted Life YearsAntineoplastic AgentsEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitorscost-effectivenessnon-small cell lung cancerOptiTROP-Lung04 trialpartitioned survival modelsacituzumab tirumotecan

Identifiers

PMID42577174
PMCPMC13453752

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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.