The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.

Human epidermal growth factor receptor 2 (HER2 or ErbB2) can be overexpressed, amplified and/or mutated in malignant tumors, and is a candidate for therapeutic targeting. However, molecular associations and clinical significances of these alterations were controversial in lung cancer. In this study,...

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Main Authors: Eun Kyung Kim, Kyung A Kim, Chang Young Lee, Hyo Sup Shim
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5287480?pdf=render
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spelling doaj-0aa346eeff9447f5a73e52a796d29b4d2020-11-25T01:52:31ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01122e017128010.1371/journal.pone.0171280The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.Eun Kyung KimKyung A KimChang Young LeeHyo Sup ShimHuman epidermal growth factor receptor 2 (HER2 or ErbB2) can be overexpressed, amplified and/or mutated in malignant tumors, and is a candidate for therapeutic targeting. However, molecular associations and clinical significances of these alterations were controversial in lung cancer. In this study, we investigated the frequency and clinicopathological significance of HER2 dysregulation in patients with lung adenocarcinoma. HER2 protein overexpression, gene amplification, and gene mutation were evaluated by immunohistochemistry (IHC), silver in situ hybridization, and direct sequencing, respectively. The H-scoring method and American Society of Clinical Oncology/College of American Pathologists breast cancer guidelines were used to interpret IHC results. Genetic analyses of EGFR and KRAS mutations, and of ALK and ROS1 rearrangements, were also performed. Of the 321 adenocarcinoma patients identified, HER2 overexpression (H-score ≥200) and gene amplification were found in 6 (1.9%) and 46 (14.3%), respectively. HER2 overexpression was correlated with papillary predominant histology; furthermore, it indicated poor overall survival and was an independent prognostic factor. HER2 amplification was associated with pleural invasion and showed a tendency towards shorter overall and disease-free survival. High-level gene amplification (HER2/CEP17 ratio ≥5 or copy number ≥10) was a poor prognostic factor for disease-free survival. HER2 mutations were detected in 6.7% (7 of 104) of driver oncogene-negative adenocarcinomas. Our study suggests that HER2 overexpression or amplification is a poor prognostic factor in lung adenocarcinoma, although the frequency of such events is low. Since molecular targeted agents are being tested in clinical trials, awareness of the specific HER2 status can influence the prognostic stratification and treatment of patients with molecularly defined subsets of lung adenocarcinoma.http://europepmc.org/articles/PMC5287480?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Eun Kyung Kim
Kyung A Kim
Chang Young Lee
Hyo Sup Shim
spellingShingle Eun Kyung Kim
Kyung A Kim
Chang Young Lee
Hyo Sup Shim
The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
PLoS ONE
author_facet Eun Kyung Kim
Kyung A Kim
Chang Young Lee
Hyo Sup Shim
author_sort Eun Kyung Kim
title The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
title_short The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
title_full The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
title_fullStr The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
title_full_unstemmed The frequency and clinical impact of HER2 alterations in lung adenocarcinoma.
title_sort frequency and clinical impact of her2 alterations in lung adenocarcinoma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Human epidermal growth factor receptor 2 (HER2 or ErbB2) can be overexpressed, amplified and/or mutated in malignant tumors, and is a candidate for therapeutic targeting. However, molecular associations and clinical significances of these alterations were controversial in lung cancer. In this study, we investigated the frequency and clinicopathological significance of HER2 dysregulation in patients with lung adenocarcinoma. HER2 protein overexpression, gene amplification, and gene mutation were evaluated by immunohistochemistry (IHC), silver in situ hybridization, and direct sequencing, respectively. The H-scoring method and American Society of Clinical Oncology/College of American Pathologists breast cancer guidelines were used to interpret IHC results. Genetic analyses of EGFR and KRAS mutations, and of ALK and ROS1 rearrangements, were also performed. Of the 321 adenocarcinoma patients identified, HER2 overexpression (H-score ≥200) and gene amplification were found in 6 (1.9%) and 46 (14.3%), respectively. HER2 overexpression was correlated with papillary predominant histology; furthermore, it indicated poor overall survival and was an independent prognostic factor. HER2 amplification was associated with pleural invasion and showed a tendency towards shorter overall and disease-free survival. High-level gene amplification (HER2/CEP17 ratio ≥5 or copy number ≥10) was a poor prognostic factor for disease-free survival. HER2 mutations were detected in 6.7% (7 of 104) of driver oncogene-negative adenocarcinomas. Our study suggests that HER2 overexpression or amplification is a poor prognostic factor in lung adenocarcinoma, although the frequency of such events is low. Since molecular targeted agents are being tested in clinical trials, awareness of the specific HER2 status can influence the prognostic stratification and treatment of patients with molecularly defined subsets of lung adenocarcinoma.
url http://europepmc.org/articles/PMC5287480?pdf=render
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