Evidence map›Paper›PMID 40413606›Full record

ArticleTherapeutic advances in respiratory disease

Excellent survival benefit achieved in patients with advanced-stage non-small cell lung cancer harboring the epidermal growth factor receptor-G719X mutation treated by afatinib: the real-world data from a multicenter study in Vietnam.

Van Luan Pham, Cam Phuong Pham, Thi Thai Hoa Nguyen, Tuan Khoi Nguyen, Minh Hai Nguyen, Thi Anh Thu Hoang, Tuan Anh Le, Dinh Thy Hao Vuong, Dac Nhan Tam Nguyen, Van Khiem Dang and 10 more

Abstract readMulticenter StudyComparative Study
In one paragraph

Article in Therapeutic advances in respiratory disease. 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

20 authors.

Van Luan PhamMilitary Central Hospital 108, Hanoi, Vietnam.ORCID 0000-0002-2291-1054
Cam Phuong PhamHanoi Medical University, Hanoi, Vietnam.ORCID 0000-0002-4342-0959
Thi Thai Hoa NguyenVietnam National Cancer Hospital, Hanoi, Vietnam.
Tuan Khoi NguyenHo Chi Minh City Oncology Hospital, Ho Chi Minh, Vietnam.
Minh Hai NguyenMilitary Central Hospital 108, Hanoi, Vietnam.
Thi Anh Thu HoangHo Chi Minh City Oncology Hospital, Ho Chi Minh, Vietnam.
Tuan Anh LeCho Ray Hospital, Ho Chi Minh, Vietnam.
Dinh Thy Hao VuongCho Ray Hospital, Ho Chi Minh, Vietnam.ORCID 0000-0001-8313-5688
Dac Nhan Tam NguyenThong Nhat Hospital, Ho Chi Minh, Vietnam.
Van Khiem DangNational Lung Hospital, Hanoi, Vietnam.
Thi Oanh NguyenNational Lung Hospital, Hanoi, Vietnam.
Hung Kien DoVietnam National Cancer Hospital, Hanoi, Vietnam.ORCID 0000-0001-6059-7046
Ha Thanh VuVietnam National Cancer Hospital, Hanoi, Vietnam.ORCID 0009-0007-3585-8460
Thi Thuy Hang NguyenVietnam National Cancer Hospital, Hanoi, Vietnam.
Van Thai PhamHanoi Medical University, Hanoi, Vietnam.ORCID 0009-0005-3073-8406
Le Huy TrinhHanoi Medical University, Hanoi, Vietnam.
Hoang Gia NguyenHanoi Oncology Hospital, Hanoi, Vietnam.ORCID 0009-0008-6759-9683
Cong Minh TruongVietnam National Cancer Hospital, Hanoi, Vietnam.ORCID 0000-0003-3953-6729
Tran Minh Chau PhamHo Chi Minh City Oncology Hospital, Ho Chi Minh, Vietnam.
Thi Bich Phuong NguyenVietnam National Cancer Hospital, Hanoi, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAfatinib is indicated for patients with advanced-stage non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) mutations, including uncommon mutations. However, the differences in survival benefits between patients with different types of EGFR mutations remain unclear.

objectivesThis study aimed to compare the effectiveness of afatinib treatment in patients harboring the EGFR-G719X mutation with that in patients carrying other uncommon EGFR mutations.

designThis was a retrospective study.

methodsNinety-two patients with locally advanced and metastatic NSCLC, of whom 49 patients with EGFR-G719X mutations that were both single and compound, and 43 patients harbored other uncommon EGFR mutations, who were treated with afatinib as first-line treatment. The patients were followed up and evaluated every 3 months or when there were symptoms of progressive disease. The endpoints were the objective response rate (ORR), time-to-treatment failure (TTF), and overall survival (OS).

resultsThe average ages of patients with the EGFR-G719X and uncommon EGFR mutations were 62.7 years and 63.1 years, respectively. There were no significant differences in sex or smoking history between the two groups. In total, 28.6% of patients with the G719X mutation and 23.3% of patients with other mutations had brain metastases. The ORR of patients with the G719X mutation was 79.6%, which was 10% higher than that of patients with other EGFR mutations. Patients harboring the EGFR-G719X mutation had median TTF and median OS periods of 19.3 months and 31.4 months, respectively, which were significantly higher than those of patients carrying other mutations at 11.2 months. Subgroup analysis showed that TTF and OS benefits were observed in female patients, patients without brain metastasis, and patients with good performance status who harbored the G719X mutation.

conclusionPatients with the EGFR-G719X mutation achieve significantly better TTF and OS benefits than those with other uncommon EGFR mutations.

Indexed as

AfatinibAntineoplastic AgentsCarcinoma, Non-Small-Cell LungLung NeoplasmsMutationProtein Kinase InhibitorsAdultAgedErbB ReceptorsFemaleHumansMaleMiddle AgedNeoplasm StagingRetrospective StudiesTime FactorsAfatinibAntineoplastic AgentsEGFR protein, humanErbB ReceptorsProtein Kinase Inhibitorsafatinib first lineG719Xnon-small cell lung canceruncommon EGFR mutations

Identifiers

PMID40413606
PMCPMC12104603

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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.