Effect of Asbestos Exposure on the Frequency of EGFR Mutations and ALK/ROS1 Rearrangements in Patients With Lung Adenocarcinoma: A Multicentric Study
dc.contributor.author | Yilmaz S. | |
dc.contributor.author | Demirci N.Y. | |
dc.contributor.author | Metintas S. | |
dc.contributor.author | Zamani A. | |
dc.contributor.author | Karadag M. | |
dc.contributor.author | Guçlu O.A. | |
dc.contributor.author | Kabalak P.A. | |
dc.contributor.author | Yilmaz U. | |
dc.contributor.author | Ak G. | |
dc.contributor.author | Kizilgoz D. | |
dc.contributor.author | Ozturk A. | |
dc.contributor.author | Yilmaz U. | |
dc.contributor.author | Batum O. | |
dc.contributor.author | Kavas M. | |
dc.contributor.author | Serifoglu I. | |
dc.contributor.author | Unsal M. | |
dc.contributor.author | Komurcuoglu B.E. | |
dc.contributor.author | Cengiz T.I. | |
dc.contributor.author | Ulubay G. | |
dc.contributor.author | Ozdemirel T.S. | |
dc.contributor.author | Ozyurek B.A. | |
dc.contributor.author | Kavurgacı S. | |
dc.contributor.author | Alizoroglu D. | |
dc.contributor.author | Celik P. | |
dc.contributor.author | Erdogan Y. | |
dc.contributor.author | In E. | |
dc.contributor.author | Aksoy A. | |
dc.contributor.author | Altin S. | |
dc.contributor.author | Gunluoglu G. | |
dc.contributor.author | Metintas M. | |
dc.date.accessioned | 2024-07-22T08:06:08Z | |
dc.date.available | 2024-07-22T08:06:08Z | |
dc.date.issued | 2021 | |
dc.description.abstract | Objective: The aim of this study is to investigate the effect of asbestos exposure on cancer-driver mutations. Methods: Between January 2014 and September 2018, epidermal growth factor receptor (EGFR), anaplastic lymphoma receptor tyrosine kinase (ALK), and c-ros oncogene 1 receptor tyrosine kinase gene (ROS1) alterations, demographic characteristics, asbestos exposure, and asbestos-related radiological findings of 1904 patients with lung adenocarcinoma were recorded. Results: The frequencies of EGFR mutations, ALK, and ROS1 rearrangements were 14.5%, 3.7%, and 0.9%, respectively. The rates of EGFR mutations and ALK rearrangements were more frequent in asbestos exposed non-smokers (48.7% and 9%, respectively). EGFR mutation rate was correlated to female gender and not-smoking, ALK rearrangement rate was correlated to younger age, not-smoking, and a history of asbestos exposure. Conclusions: The higher rate of ALK rearrangements in asbestos-exposed lung adenocarcinoma cases shows that asbestos exposure may most likely cause genetic alterations that drive pulmonary adenocarcinogenesis. Copyright © 2020 American College of Occupational and Environmental Medicine. | |
dc.identifier.DOI-ID | 10.1097/JOM.0000000000002115 | |
dc.identifier.issn | 10762752 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/13376 | |
dc.language.iso | English | |
dc.publisher | Lippincott Williams and Wilkins | |
dc.subject | Adenocarcinoma of Lung | |
dc.subject | Anaplastic Lymphoma Kinase | |
dc.subject | Asbestos | |
dc.subject | ErbB Receptors | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Lung Neoplasms | |
dc.subject | Mutation | |
dc.subject | Oncogenes | |
dc.subject | Protein-Tyrosine Kinases | |
dc.subject | Proto-Oncogene Proteins | |
dc.subject | anaplastic lymphoma kinase | |
dc.subject | asbestos | |
dc.subject | EGFR protein, human | |
dc.subject | epidermal growth factor receptor | |
dc.subject | oncoprotein | |
dc.subject | protein tyrosine kinase | |
dc.subject | ROS1 protein, human | |
dc.subject | clinical trial | |
dc.subject | female | |
dc.subject | genetics | |
dc.subject | human | |
dc.subject | lung adenocarcinoma | |
dc.subject | lung tumor | |
dc.subject | multicenter study | |
dc.subject | mutation | |
dc.subject | oncogene | |
dc.title | Effect of Asbestos Exposure on the Frequency of EGFR Mutations and ALK/ROS1 Rearrangements in Patients With Lung Adenocarcinoma: A Multicentric Study | |
dc.type | Article |