Evidence map›Paper›PMID 42369726›Full record

ArticleTherapeutic advances in medical oncology2026

Clinical characteristics and outcomes of advanced EGFR-mutated NSCLC treated with 45 or 30 mg starting doses of dacomitinib: a retrospective multicenter analysis.

Ping-Chih Hsu, How-Wen Ko, Li-Chung Chiu, Shih-Hong Li, Shih-Hao Huang, Chung-Shu Lee, Yu-Ching Lin, Scott Chih-Hsi Kuo, Jia-Shiuan Ju, Chin-Chou Wang and 1 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 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
–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

11 authors.

Ping-Chih HsuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.ORCID https://orcid.org/0000-0003-0173-7509
How-Wen KoDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.ORCID https://orcid.org/0000-0002-6415-2965
Li-Chung ChiuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.
Shih-Hong LiDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.ORCID https://orcid.org/0000-0003-3755-0287
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.ORCID https://orcid.org/0000-0003-3309-937X
Jia-Shiuan JuDivision of Thoracic Medicine, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Taoyuan City, Taiwan.ORCID https://orcid.org/0009-0001-2285-2787
Chin-Chou WangDepartment of Medicine, College of Medicine, Chang Gung University, Taoyuan City, Taiwan.
Cheng-Ta YangDepartment of Thoracic Medicine, Chang Gung Memorial Hospital, 123 Dinghu Road, Gueishen District, Taoyuan City 33378, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The evidence from studies comparing 45 and 30 mg starting doses of first-line dacomitinib for advanced epidermal growth factor receptor (EGFR)-mutated non-small-cell lung cancer (NSCLC) remains limited. Objectives: This study aimed to compare the clinical efficacy and safety of two starting-dose first-line dacomitinib strategies in patients with advanced EGFR-mutated NSCLC. Design: This study employed a multicenter retrospective cohort design. Methods: A total of 189 patients with stage IIIB/IV EGFR-mutated NSCLC who received first-line dacomitinib between October 2020 and September 2023 at one of four Taiwanese centers were analyzed. Among them, 59 patients started with 45 mg and 130 patients started with 30 mg. Results: The 45-mg group included significantly more male patients and had higher baseline body weight and body mass index. The objective response rate (ORR) and disease control rate were comparable between the 45-mg (72.9% and 94.9%) and 30-mg (66.9% and 91.5%) groups ( Conclusion: This study suggests that a 30-mg starting dose of dacomitinib may provide similar efficacy with improved tolerability compared with 45 mg. Prospective noninferiority studies are warranted to confirm these findings.

Indexed as

30 mg starting dose45 mg starting dosedacomitinibepidermal growth factor receptor mutationnon-small-cell lung cancer (NSCLC)tyrosine kinase inhibitor

Identifiers

PMID42369726
PMCPMC13305405

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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.