Cargando…

Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR

The aim of this study was to determine the distribution of known oncogenic driver mutations in female never-smoker Asian patients with lung adenocarcinoma. We analyzed 214 mutations across 26 lung cancer-associated genes and three fusion genes using the MassARRAY® LungCarta Panel and the ALK, ROS1,...

Descripción completa

Detalles Bibliográficos
Autores principales: Ha, Sang Yun, Choi, So-Jung, Cho, Jong Ho, Choi, Hye Joo, Lee, Jinseon, Jung, Kyungsoo, Irwin, Darry, Liu, Xiao, Lira, Maruja E., Mao, Mao, Kim, Hong Kwan, Choi, Yong Soo, Shim, Young Mog, Park, Woong Yang, Choi, Yoon-La, Kim, Jhingook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467161/
https://www.ncbi.nlm.nih.gov/pubmed/25760072
_version_ 1782376338506645504
author Ha, Sang Yun
Choi, So-Jung
Cho, Jong Ho
Choi, Hye Joo
Lee, Jinseon
Jung, Kyungsoo
Irwin, Darry
Liu, Xiao
Lira, Maruja E.
Mao, Mao
Kim, Hong Kwan
Choi, Yong Soo
Shim, Young Mog
Park, Woong Yang
Choi, Yoon-La
Kim, Jhingook
author_facet Ha, Sang Yun
Choi, So-Jung
Cho, Jong Ho
Choi, Hye Joo
Lee, Jinseon
Jung, Kyungsoo
Irwin, Darry
Liu, Xiao
Lira, Maruja E.
Mao, Mao
Kim, Hong Kwan
Choi, Yong Soo
Shim, Young Mog
Park, Woong Yang
Choi, Yoon-La
Kim, Jhingook
author_sort Ha, Sang Yun
collection PubMed
description The aim of this study was to determine the distribution of known oncogenic driver mutations in female never-smoker Asian patients with lung adenocarcinoma. We analyzed 214 mutations across 26 lung cancer-associated genes and three fusion genes using the MassARRAY® LungCarta Panel and the ALK, ROS1, and RET fusion assays in 198 consecutively resected lung adenocarcinomas from never-smoker females at a single institution. EGFR mutation, which was the most frequent driver gene mutation, was detected in 124 (63%) cases. Mutation of ALK, KRAS, PIK3CA, ERBB2, BRAF, ROS1, and RET genesoccurred in 7%, 4%, 2.5%, 1.5%, 1%, 1%, and 1% of cases, respectively. Thus, 79% of lung adenocarcinomas from never-smoker females harbored well-known oncogenic mutations. Mucinous adenocarcinomas tended to have a lower frequency of known driver gene mutations than other histologic subtypes. EGFR mutation was associated with older age and a predominantly acinar pattern, while ALK rearrangement was associated with younger age and a predominantly solid pattern. Lung cancer in never-smoker Asian females is a distinct entity, with the majority of these cancers developing from oncogenic mutations.
format Online
Article
Text
id pubmed-4467161
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-44671612015-06-22 Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR Ha, Sang Yun Choi, So-Jung Cho, Jong Ho Choi, Hye Joo Lee, Jinseon Jung, Kyungsoo Irwin, Darry Liu, Xiao Lira, Maruja E. Mao, Mao Kim, Hong Kwan Choi, Yong Soo Shim, Young Mog Park, Woong Yang Choi, Yoon-La Kim, Jhingook Oncotarget Clinical Research Paper The aim of this study was to determine the distribution of known oncogenic driver mutations in female never-smoker Asian patients with lung adenocarcinoma. We analyzed 214 mutations across 26 lung cancer-associated genes and three fusion genes using the MassARRAY® LungCarta Panel and the ALK, ROS1, and RET fusion assays in 198 consecutively resected lung adenocarcinomas from never-smoker females at a single institution. EGFR mutation, which was the most frequent driver gene mutation, was detected in 124 (63%) cases. Mutation of ALK, KRAS, PIK3CA, ERBB2, BRAF, ROS1, and RET genesoccurred in 7%, 4%, 2.5%, 1.5%, 1%, 1%, and 1% of cases, respectively. Thus, 79% of lung adenocarcinomas from never-smoker females harbored well-known oncogenic mutations. Mucinous adenocarcinomas tended to have a lower frequency of known driver gene mutations than other histologic subtypes. EGFR mutation was associated with older age and a predominantly acinar pattern, while ALK rearrangement was associated with younger age and a predominantly solid pattern. Lung cancer in never-smoker Asian females is a distinct entity, with the majority of these cancers developing from oncogenic mutations. Impact Journals LLC 2015-02-28 /pmc/articles/PMC4467161/ /pubmed/25760072 Text en Copyright: © 2015 Ha et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Ha, Sang Yun
Choi, So-Jung
Cho, Jong Ho
Choi, Hye Joo
Lee, Jinseon
Jung, Kyungsoo
Irwin, Darry
Liu, Xiao
Lira, Maruja E.
Mao, Mao
Kim, Hong Kwan
Choi, Yong Soo
Shim, Young Mog
Park, Woong Yang
Choi, Yoon-La
Kim, Jhingook
Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title_full Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title_fullStr Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title_full_unstemmed Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title_short Lung cancer in never-smoker Asian females is driven by oncogenic mutations, most often involving EGFR
title_sort lung cancer in never-smoker asian females is driven by oncogenic mutations, most often involving egfr
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467161/
https://www.ncbi.nlm.nih.gov/pubmed/25760072
work_keys_str_mv AT hasangyun lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT choisojung lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT chojongho lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT choihyejoo lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT leejinseon lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT jungkyungsoo lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT irwindarry lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT liuxiao lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT liramarujae lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT maomao lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT kimhongkwan lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT choiyongsoo lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT shimyoungmog lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT parkwoongyang lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT choiyoonla lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr
AT kimjhingook lungcancerinneversmokerasianfemalesisdrivenbyoncogenicmutationsmostofteninvolvingegfr