Evidence map›Paper›PMID 27449093›Full record

ArticleOncotarget2016

Higher frequency but random distribution of EGFR mutation subtypes in familial lung cancer patients.

Kuo-Hsuan Hsu, Jeng-Sen Tseng, Chih-Liang Wang, Tsung-Ying Yang, Chien-Hua Tseng, Hsuan-Yu Chen, Kun-Chieh Chen, Chi-Ren Tsai, Cheng-Ta Yang, Sung-Liang Yu and 10 more

Open access · diamondAbstract readMulticenter Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 24% of its field
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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. High-Penetrance Rare Variants Underlying Familial Lung Cancer Risk: Insights From Genetic Epidemiology of Lung Cancer Consortium.Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Inherited lung cancer syndromes targeting never smokers.Translational lung cancer research · 2018
    Review
  8. 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 at 10 institutions in 1 country.

Kuo-Hsuan HsuInstitute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan.
Jeng-Sen TsengDivision of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Chih-Liang WangDepartment of Thoracic Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Tsung-Ying YangDivision of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Chien-Hua TsengInstitute of Epidemiology and Preventive Medicine, National Taiwan University, Taipei, Taiwan.
Hsuan-Yu ChenInstitute of Statistical Science, Academia Sinica, Taipei, Taiwan.
Kun-Chieh ChenDivision of Chest Medicine, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Chi-Ren TsaiDepartment of Pediatrics, Taichung Veterans General Hospital, Taichung, Taiwan.
Cheng-Ta YangDepartment of Thoracic Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Sung-Liang YuDepartment of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Kang-Yi SuDepartment of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Chong-Jen YuDivision of Pulmonary Medicine, Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Chao-Chi HoDivision of Pulmonary Medicine, Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Te-Chun HsiaDepartment of Internal Medicine, China Medical University Hospital, Taichung, Taiwan.
Ming-Fang WuDivisions of Medical Oncology and Pulmonary Medicine, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung, Taiwan.
Kuo-Liang ChiuDivision of Chest Medicine, Department of Internal Medicine, Taichung Tzu-Chi Hospital, Taichung, Taiwan.
Chien-Ming LiuDivision of Chest Medicine, Department of Internal Medicine, Taichung Tzu-Chi Hospital, Taichung, Taiwan.
Pan-Chyr YangDivision of Pulmonary Medicine, Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Jeremy J W ChenInstitute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan.
Gee-Chen ChangInstitute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan.
National Taiwan University · TWNational Taiwan University Hospital · TWTaichung Veterans General Hospital · TWChang Gung Memorial Hospital · TWNational Chung Hsing University · TWNational Yang Ming Chiao Tung University · TWChina Medical University Hospital · TWChung Shan Medical University · TWInstitute of Statistical Science, Academia Sinica · TWTzu Chi University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the advancement of epidermal growth factor receptor (EGFR) inhibitors in lung cancer therapy, it remains unclear whether EGFR mutation status in familial lung cancers is different from that of sporadic cases. In this multicenter retrospective study, we compared both the EGFR mutation frequency and patterns between familial and sporadic cases. The results explored that family history of lung cancer is an independent predictor for higher EGFR mutation rate in 1713 lung adenocarcinoma patients (Odd ratio 1.68, 95% CI 1.06-2.67, P = 0.028). However, the distribution of EGFR mutation subtypes was similar to that of sporadic cases. Part of our study involved 40 lung cancer families with at least 2 tumor tissues available within each single family (n = 88) and there was no familial aggregation pattern in EGFR mutation subtypes. There were two families harboring the YAP1 R331W germline risk allele and EGFR mutation statuses among YAP1 family members also varied. These phenomena may hint at the direction of future research into lung carcinogenesis and EGFR mutagenesis.

Indexed as

MutationAdenocarcinomaAgedDNA Mutational AnalysisErbB ReceptorsFamily HealthFemaleGene FrequencyHumansLogistic ModelsLung NeoplasmsMaleMiddle AgedRetrospective StudiesEGFR protein, humanErbB Receptorsepidermal growth factor receptor (EGFR)familial lung cancernon-small cell lung cancerYAP1

Identifiers

PMID27449093
PMCPMC5288187
OpenAlexW2491081100

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.