Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations

Abstract 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 Jan...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Hyun Woo Lee, Young Sik Park, Sangshin Park, Chang-Hoon Lee
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2020
Materias:
R
Q
Acceso en línea:https://doaj.org/article/42a26d4640764645aa4fd4e479833fb3
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:42a26d4640764645aa4fd4e479833fb3
record_format dspace
spelling oai:doaj.org-article:42a26d4640764645aa4fd4e479833fb32021-12-02T19:12:25ZPoor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations10.1038/s41598-020-71996-72045-2322https://doaj.org/article/42a26d4640764645aa4fd4e479833fb32020-09-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-71996-7https://doaj.org/toc/2045-2322Abstract 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.Hyun Woo LeeYoung Sik ParkSangshin ParkChang-Hoon LeeNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Hyun Woo Lee
Young Sik Park
Sangshin Park
Chang-Hoon Lee
Poor prognosis of NSCLC located in lower lobe is partly mediated by lower frequency of EGFR mutations
description Abstract 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 article
author Hyun Woo Lee
Young Sik Park
Sangshin Park
Chang-Hoon Lee
author_facet Hyun Woo Lee
Young Sik Park
Sangshin Park
Chang-Hoon Lee
author_sort Hyun Woo Lee
title 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_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_sort poor prognosis of nsclc located in lower lobe is partly mediated by lower frequency of egfr mutations
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/42a26d4640764645aa4fd4e479833fb3
work_keys_str_mv AT hyunwoolee poorprognosisofnsclclocatedinlowerlobeispartlymediatedbylowerfrequencyofegfrmutations
AT youngsikpark poorprognosisofnsclclocatedinlowerlobeispartlymediatedbylowerfrequencyofegfrmutations
AT sangshinpark poorprognosisofnsclclocatedinlowerlobeispartlymediatedbylowerfrequencyofegfrmutations
AT changhoonlee poorprognosisofnsclclocatedinlowerlobeispartlymediatedbylowerfrequencyofegfrmutations
_version_ 1718377044943831040