Evidence map›Paper›PMID 39206619›Full record

ArticleCancer medicine2024

Cost-effectiveness analysis of osimertinib plus chemotherapy for patients with EGFR-mutated advanced non-small cell lung cancer.

Wentao Tian, Lishui Niu, Rongrong Zhou, Ziqi Wang, Jiaoyang Ning, Ruoyu Lu, Yin Shi, Zhaohua Tan

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Central nervous system efficacy of third generationJournal of thoracic disease · 2026
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  10. Adagrasib in the treatment of KRASTranslational cancer research · 2025
    Article
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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.

Wentao TianDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0002-8938-7576
Lishui NiuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Rongrong ZhouDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.ORCID 0000-0003-4483-0615
Ziqi WangDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jiaoyang NingDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Ruoyu LuDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Yin ShiXiangya Lung Cancer Center, Xiangya Hospital, Central South University, Changsha, China.
Zhaohua TanDepartment of Oncology, Xiangya Hospital, Central South University, Changsha, Hunan, China.

Funding

Chen Xiao-Ping Foundation for the Development of Science and Technology of Hubei Province CXPJJH121005-01National Multidisciplinary Cooperative Diagnosis and Treatment Capacity Building Project for Major Diseases z027002Natural Science Foundation of Hunan Province 2022JJ30992
6 · The paper itself

Abstract

introductionFirst-line osimertinib plus chemotherapy significantly prolonged progression-free survival of patients with EGFR-mutated advanced non-small cell lung cancer (NSCLC) compared to osimertinib, according to the FLAURA2 trial.

methodsWe established a Markov model to compare the cost-effectiveness of osimertinib plus chemotherapy with that of osimertinib alone. Clinical data were obtained from the FLAURA and FLAURA2 trials, and additional data were extracted from online resources and publications. Sensitivity analyses were conducted to evaluate the robustness of the findings. We used A willingness-to-pay threshold of $150,000 per quality-adjusted life-years (QALYs) gained. The main outcomes were QALYs, overall costs, incremental cost-effectiveness ratio (ICER), incremental net monetary benefit, and incremental net health benefit. Subgroup analyses were conducted according to patients' mutation type and central nervous system (CNS) metastatic status.

resultsIn a 20-year time horizon, the ICER of osimertinib plus chemotherapy versus osimertinib alone was $223,727.1 per QALY gained. The sensitivity analyses identified the cost of osimertinib and the hazard ratio for overall survival as the top 2 influential factors and a 1.9% probability of osimertinib plus chemotherapy to be cost-effective. The subgroup analyses revealed ICERs of $132,614.1, $224,449.8, $201,464.1, and $130,159.7 per QALY gained for L858R mutations, exon 19 deletions, CNS metastases, and no CNS metastases subgroups, respectively.

conclusionsFrom the perspective of the United States health care system, osimertinib plus chemotherapy is not cost-effective compared to osimertinib alone for treatment-naïve patients with EGFR-mutated advanced NSCLC, but more favorable cost-effectiveness occurs in patients with L858R mutations and patients without baseline CNS metastases.

Indexed as

AcrylamidesAniline CompoundsAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, Non-Small-Cell LungCost-Benefit AnalysisErbB ReceptorsLung NeoplasmsMutationQuality-Adjusted Life YearsCost-Effectiveness AnalysisFemaleHumansIndolesMaleMarkov ChainsProgression-Free SurvivalAcrylamidesAniline CompoundsEGFR protein, humanErbB ReceptorsIndolesosimertinibPyrimidineschemotherapycost‐effectivenessEGFRnon‐small cell lung cancerosimertinib

Identifiers

PMID39206619
PMCPMC11358701

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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.