Evidence map›Paper›PMID 41761381›Full record

Observational studyCancer medicine2026

Dacomitinib as a First-Line Therapy for Advanced EGFR-Mutated Non-Small Cell Lung Cancer Without Brain Metastases: A Multicenter Retrospective Observational Study.

Ping-Chih Hsu, How-Wen Ko, Li-Chung Chiu, Shih-Hao Huang, Chung-Shu Lee, Yu-Ching Lin, Scott Chih-Hsi Kuo, Jia-Shiuan Ju, Chin-Chou Wang, Cheng-Ta Yang

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Cancer medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Ping-Chih HsuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
How-Wen KoDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
Li-Chung ChiuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
Shih-Hao HuangDepartment of Thoracic Medicine, New Taipei Municipal TuCheng Hospital, New Taipei City, Taiwan.
Chung-Shu LeeDepartment of Medicine, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Yu-Ching LinDepartment of Medicine, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Scott Chih-Hsi KuoDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
Jia-Shiuan JuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
Chin-Chou WangDepartment of Medicine, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Cheng-Ta YangDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.

Funding

Chang Gung Memorial Hospital, Linkou CMRPG3N1331
6 · The paper itself

Abstract

backgroundReal-world evidence regarding the use of dacomitinib as a first-line therapy for advanced non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations remains limited. This multicenter, retrospective cohort study aimed to evaluate the clinical outcomes of dacomitinib as a first-line treatment in patients with untreated advanced EGFR-mutant NSCLC without brain metastases. PATIENTS AND

methodsThis retrospective analysis included 161 patients with stage IIIB/IV EGFR-mutant NSCLC without brain metastasis at baseline who received first-line dacomitinib between October 2020 and August 2023 at four Taiwanese cancer centers. The primary outcomes included the objective response rate (ORR), progression-free survival (PFS), overall survival (OS), predictive risk factors for PFS, and adverse events (AEs).

resultsThe ORR was 64.0%, and the disease control rate (DCR) reached 91.3%. The median PFS was 20.93 months (95% CI: 17.55-24.32), and the median OS was 41.27 months (95% CI: 31.71-50.82). Multivariate analysis revealed that an Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≥ 2, bone metastasis, and liver metastasis were independent predictors of shorter PFS. Among patients who experienced disease progression and underwent rebiopsy, the secondary T790M mutation rate was 50.6%. Most treatment-related AEs were grade 1-2 and manageable.

conclusionsDacomitinib demonstrated favorable efficacy and tolerability as a first-line therapy in advanced NSCLC patients with common EGFR mutations (exon 19 deletion or L858R). A baseline ECOG PS ≥ 2 and the presence of bone or liver metastases were significantly associated with worse PFS, suggesting a need for additional therapeutic strategies in these subgroups.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsProtein Kinase InhibitorsQuinazolinonesAdultAgedAged, 80 and overBrain NeoplasmsErbB ReceptorsFemaleHumansMaleMiddle AgedMutationProgression-Free SurvivalRetrospective StudiesdacomitinibEGFR protein, humanErbB ReceptorsProtein Kinase InhibitorsQuinazolinonescommon EGFR mutationdacomitinibepidermal growth factor receptor mutationnon‐small cell lung cancer (NSCLC)tyrosine kinase inhibitor

Identifiers

PMID41761381
PMCPMC12948714

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Registered trials

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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.