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Comparison of clinical characteristics between patients with ALK-positive and EGFR-positive lung adenocarcinoma

Cited 45 time in Web of Science Cited 50 time in Scopus
Authors

Kang, Hyo Jae; Lim, Hyo-Jeong; Park, Jong Sun; Cho, Young-Jae; Yoon, Ho-Il; Chung, Jin-Haeng; Lee, Jae Ho; Lee, Choon-Taek

Issue Date
2014-02
Publisher
W. B. Saunders Co., Ltd.
Citation
Respiratory Medicine, Vol.108 No.2, pp.388-394
Abstract
Background: The discovery of the chromosomal fusion product of anaplastic lymphoma kinase (ALK) with echinoderm microtubule-associated protein-like 4 (EML4) (EML4-ALK) has changed the treatment paradigm of lung cancer. In this study, we analysed the clinical characteristics, including bronchoscopic findings, of patients with EML4-ALK-positive adenocarcinoma and compared them with those of EGFR mutation-positive patients. Materials and methods: In this retrospective cohort study, the clinical characteristics and bronchoscopic findings of patients with ALK fusion-positive lung cancers were compared to patients with EGFR-mutant lung cancers. Results: Among the 440 patients with adenocarcinoma of lung screened for this study, 46 (10.4%) harboured the EML4-ALK fusion, 90 (20.4%) harboured an activating EGFR mutation, and all had adenocarcinoma. In univariate analysis, ALK-positive patients were significantly younger than EGFR-positive patients (p = 0.004) and were more commonly male (p = 0.021). An initial status of stage IV metastatic cancer was more frequently noted in EML4-ALK-positive patients (p = 0.012), with initial brain metastasis frequently observed (p = 0.007). Compared with EGFR-positive patients, EML4-ALK-positive patients were significantly more likely to have positive bronchoscopic findings, which suggested a more centralized origin (p = 0.001). EML4-ALK patients also had significantly more positive bronchoscopic findings and were more commonly male in multivariate analysis. Conclusions: The EML4-ALK fusion defines a new molecular subset of NSCLC that has distinct clinical and bronchoscopic findings suggesting more proximal origin when compared to tumours harbouring EGFR mutations. (C) 2013 Elsevier Ltd. All rights reserved.
ISSN
0954-6111
URI
https://hdl.handle.net/10371/217088
DOI
https://doi.org/10.1016/j.rmed.2013.11.020
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  • College of Medicine
  • Department of Medicine
Research Area Interstitial lung disease, Pneumonia, Pulmonary fibrosis, 간질성 폐질환, 폐렴, 폐섬유증

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