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Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations
It is controversial whether a tumor located in the lower lobe is related with worse outcome of non-small cell lung cancer (NSCLC). This study aimed to clarify the prognostic role of primary tumor location in NSCLC. Patients newly diagnosed with NSCLC in a tertiary referral hospital from January 2011...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483476/ https://www.ncbi.nlm.nih.gov/pubmed/32913267 http://dx.doi.org/10.1038/s41598-020-71996-7 |
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author | Lee, Hyun Woo Park, Young Sik Park, Sangshin Lee, Chang-Hoon |
author_facet | Lee, Hyun Woo Park, Young Sik Park, Sangshin Lee, Chang-Hoon |
author_sort | Lee, Hyun Woo |
collection | PubMed |
description | It is controversial whether a tumor located in the lower lobe is related with worse outcome of non-small cell lung cancer (NSCLC). This study aimed to clarify the prognostic role of primary tumor location in NSCLC. Patients newly diagnosed with NSCLC in a tertiary referral hospital from January 2011 to December 2014 were followed up for 5 years. Of the 2,289 NSCLC cases, 911 (39.8%) cases pertained to lower lobe cancers. Patients with lower lobe cancer showed a higher all-cause mortality rate than those with non-lower lobe cancer (48.6% vs. 40.3%, p < 0.001). Patients with lower lobe cancer had a lower proportion of adenocarcinoma histology and epidermal growth factor receptor (EGFR) mutations. Furthermore, compared to patients with non-lower lobe cancer, those with lower lobe cancer had a higher level of tumor markers (neuron-specific enolase and cytokeratin fragment 21-1). Mediation analysis revealed that the association between lower lobe cancer and higher all-cause mortality could be explained by an indirect pathway through EGFR mutations (percent mediated = 17.3%, p = 0.005). The sensitivity analysis for adenocarcinoma patients showed similar results (percent mediated = 18.8%, p = 0.021). Lower lobe cancer is associated with a higher all-cause mortality risk in patients with NSCLC, which is partly mediated by a lower proportion of EGFR mutations. |
format | Online Article Text |
id | pubmed-7483476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74834762020-09-15 Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations Lee, Hyun Woo Park, Young Sik Park, Sangshin Lee, Chang-Hoon Sci Rep Article It is controversial whether a tumor located in the lower lobe is related with worse outcome of non-small cell lung cancer (NSCLC). This study aimed to clarify the prognostic role of primary tumor location in NSCLC. Patients newly diagnosed with NSCLC in a tertiary referral hospital from January 2011 to December 2014 were followed up for 5 years. Of the 2,289 NSCLC cases, 911 (39.8%) cases pertained to lower lobe cancers. Patients with lower lobe cancer showed a higher all-cause mortality rate than those with non-lower lobe cancer (48.6% vs. 40.3%, p < 0.001). Patients with lower lobe cancer had a lower proportion of adenocarcinoma histology and epidermal growth factor receptor (EGFR) mutations. Furthermore, compared to patients with non-lower lobe cancer, those with lower lobe cancer had a higher level of tumor markers (neuron-specific enolase and cytokeratin fragment 21-1). Mediation analysis revealed that the association between lower lobe cancer and higher all-cause mortality could be explained by an indirect pathway through EGFR mutations (percent mediated = 17.3%, p = 0.005). The sensitivity analysis for adenocarcinoma patients showed similar results (percent mediated = 18.8%, p = 0.021). Lower lobe cancer is associated with a higher all-cause mortality risk in patients with NSCLC, which is partly mediated by a lower proportion of EGFR mutations. Nature Publishing Group UK 2020-09-10 /pmc/articles/PMC7483476/ /pubmed/32913267 http://dx.doi.org/10.1038/s41598-020-71996-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lee, Hyun Woo Park, Young Sik Park, Sangshin Lee, Chang-Hoon Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title | Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title_full | Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title_fullStr | Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title_full_unstemmed | Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title_short | Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations |
title_sort | poor prognosis of nsclc located in lower lobe is partly mediated by lower frequency of egfr mutations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483476/ https://www.ncbi.nlm.nih.gov/pubmed/32913267 http://dx.doi.org/10.1038/s41598-020-71996-7 |
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