Evidence map›Paper›PMID 41051581›Full record

ArticleDiscover oncology2025

Clinical study of aumolertinib versus osimertinib in the treatment of EGFR-mutated advanced non-small cell lung cancer.

Sheng-Xi Yang, Jia-De Zhu, Ling Ma, Yan Pan, Qiu-Rui Li, Wen-Lian Tu, Zhi-Qing Zhang

Abstract read
In one paragraph

Article in Discover oncology, 2025. 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
–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

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

7 authors.

Sheng-Xi Yang *Department of Clinical Pharmacy, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032, China.
Jia-De Zhu *Department of Pharmacy, The People's Hospital of Yongshan County, Zhaotong, 657300, China.
Ling MaDepartment of Clinical Pharmacy, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032, China.
Yan PanDepartment of Clinical Pharmacy, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032, China.
Qiu-Rui LiDepartment of Pharmacy, The People's Hospital of Chuxiong Yi Autonomo, Chuxiong, 675000, China.
Wen-Lian TuDepartment of Clinical Pharmacy, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032, China. tuwenlian18@aliyun.com.
Zhi-Qing ZhangDepartment of Clinical Pharmacy, The First People's Hospital of Yunnan Province/The Affiliated Hospital of Kunming University of Science and Technology, Kunming, 650032, China. 564267128@qq.com.

Funding

the Science and Technology Department of Yunnan Province (Joint Special Project of Kunming Medical University) 202201AY070001-238
6 · The paper itself

Abstract

backgroundTo compare the efficacy and safety of aumolertinib and osimertinib in the treatment of advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations.

methodsA retrospective analysis was performed for patients with EGFR-mutant NSCLC. The primary outcome was median progression-free survival (mPFS). Kaplan-Meier curves and the log-rank test were used to evaluate PFS and overall survival (OS), Cox regression was used for prognostic factors assessment.

resultsA total of 202 patients were included, comprising 106 aumolertinib users and 96 osimertinib users. In the first-line treatment, no significant difference was observed in mPFS between aumolertinib and osimertinib group (19.0 months; hazard ratio [HR], 1.15; 95% confidence interval [CI], 0.70-1.91; P = 0.58). The disease control rate (DCR) (95.7% vs. 89.8%), objective response rate (ORR) (39.1% vs. 30.6%), and median OS (27.0 vs. 38.0 months) were comparable between the two groups, with no statistical significance. In the second-line treatment, aumolertinib and osimertinib demonstrated similar mPFS (13.5 vs. 13.0 months; HR, 1.13; 95% CI, 0.75-1.71; P = 0.55), DCR (90.0% vs. 87.2%), ORR (16.7% vs. 17.0%), and median OS (24.0 vs. 20.0 months). Adverse events of grade 1-2 were also similar between the two groups. Cox regression revealed that performance status (P < 0.001) and the treatment lines of aumolertinib/osimertinib (P = 0.015) were independent prognostic factors.

conclusionAumolertinib and osimertinib exhibit comparable efficacy and safety profiles in the treatment of EGFR-mutant NSCLC, providing a reference path for clinicians to optimize drug treatment strategies in NSCLC.

Indexed as

AumolertinibEGFRNSCLCOsimertinib

Identifiers

PMID41051581
PMCPMC12500483

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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.