Evidence map›Paper›PMID 40349136›Full record

ArticleThe oncologist2025

Efficacy and safety of dacomitinib in treatment-naïve patients with advanced NSCLC and brain metastasis: a multicenter cohort study.

Puyuan Xing, Xingxiang Pu, Yu Zhou, Ziling Liu, Yu Yao, Jiayu Liu, Shouzheng Wang, Ying Hu, Junling Li, Lin Wu

Abstract readMulticenter Study
In one paragraph

Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Puyuan XingDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, People's Republic of China.ORCID 0000-0003-4415-9892
Xingxiang PuThe Second Department of Thoracic Oncology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha, 410013,People's Republic of China.
Yu ZhouThe Second Department of Thoracic Oncology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha, 410013,People's Republic of China.
Ziling LiuDepartment of Oncology, the First Hospital of Jilin University, Changchun, 130031, People's Republic of China.
Yu YaoDepartment of Oncology, the First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, People's Republic of China.
Jiayu LiuDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, People's Republic of China.
Shouzheng WangThe Department of Oncology, Beijing Chest Hospital, Beijing, 101149, People's Republic of China.
Ying HuThe Department of Oncology, Beijing Chest Hospital, Beijing, 101149, People's Republic of China.
Junling LiDepartment of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, 100021, People's Republic of China.ORCID 0000-0002-7361-325X
Lin WuThe Second Department of Thoracic Oncology, The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University/Hunan Cancer Hospital, Changsha, 410013,People's Republic of China.ORCID 0000-0001-7078-7767

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-2019Genecast-024Hunan Cancer Hospital Climb Plan ZX2020005-5Hunan Provincial Health High-Level Talent Scientific Research Project R2023125National Key Clinical Specialty Scientific Research Project Z2023098
6 · The paper itself

Abstract

backgroundThe data for dacomitinib, a second-generation EGFR-TKI, treating patients with advanced non-small cell lung cancer (NSCLC) and brain metastasis was lacking. This study aimed to explore the efficacy and safety of dacomitinib in treating EGFR-mutated advanced NSCLC with brain metastasis in first-line settings.

methodsEligible patients were treatment-naïve advanced NSCLC patients with ≥1 brain metastasis no less than 5 mm treated with dacomitinib. The primary endpoint was intracranial objective response rate (ORR). Secondary endpoints included intracranial and extracranial progression-free survival (PFS), overall survival (OS), intracranial and extracranial ORR, disease control rate (DCR), and safety. The response was evaluated per modified Response Evaluation Criteria in Solid Tumors (mRECIST) and RANO-BM (Response Assessment in Neuro-Oncology Brain Metastases) criteria.

resultBetween July 2nd, 2019, and September 30th, 2022, a total of 87 treatment-naïve patients with advanced NSCLC and brain metastasis treated with dacomitinib from four hospitals were included. The data cutoff date was March 24th, 2023, and the median duration of follow-up time was 17.5 months (range 1.6-34.7 months). Based on mRECIST criteria, for all the 87 patients with evaluable brain metastasis, the iORR was 89.7% (95%CI, 81.3%-95.2%) and iDCR was 97.7% (95%CI, 91.9-99.7%), with 42 patients achieving CR, 36 patients achieving PR, and 7 patients maintaining SD. Based on RANO-BM criteria, the iORR was 71.3% (62/87, 95%CI 60.6%-80.5%) and iDCR was 97.7% (85/87, 95%CI, 91.9%-99.7%), with 42 patients achieving CR, 20 patients achieving PR, and 23 patients maintaining SD (Table). Median iPFS was 26.0 (95%CI, 20.7-31.4) months, and the 1-year and 2-year iPFS rate were 68.9% and 51.5%, respectively. Of 75 patients with evaluable extracranial lesions, 2 patients achieved CR (2.7%), the systemic ORR was 73.8% (95%CI 63.1%-82.8%) and DCR was 96.4% (89.9%-99.3%) (Table). Systemic median PFS was 14.0 (95%CI 11.1-16.9) months and median OS was 34.0 (95%CI 28.0-39.9) months. Overall, 86 of 87 (98.9%) patients experienced adverse events (AEs) of any grade. The most common (≥20%) AEs including rash (89.7%), oral ulcer (74.2%), diarrhea (67.8%), and paronychia (59.8%). Most of the AEs were grade 1 or grade 2 and no patients died due to severe AEs.

conclusionsDacomitinib showed promising efficacy and a manageable safety profile for advanced NSCLC with brain metastasis harboring EGFR mutation in the first-line treatment.

Indexed as

Brain NeoplasmsCarcinoma, Non-Small-Cell LungLung NeoplasmsProtein Kinase InhibitorsQuinazolinonesAdultAgedAged, 80 and overCohort StudiesFemaleHumansMaleMiddle AgeddacomitinibProtein Kinase InhibitorsQuinazolinonesbrain metastasisdacomitinibEGFRnon-small cell lung cancertreatment

Identifiers

PMID40349136
PMCPMC12065940

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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.