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Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer

BACKGROUND/AIMS: The treatment of epidermal growth factor receptor (EGFR)-mutated lung cancer cases has shown remarkable development in the past two decades. However, there have been limited studies comparing the prognostic effects of EGFR-tyrosine kinase inhibitor (TKI) and other treatment modaliti...

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Autores principales: Jang, Seung Hun, Lee, Dong Yoon, Jeong, Jihyeon, Choi, Won-Il
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271728/
https://www.ncbi.nlm.nih.gov/pubmed/35811369
http://dx.doi.org/10.3904/kjim.2021.488
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author Jang, Seung Hun
Lee, Dong Yoon
Jeong, Jihyeon
Choi, Won-Il
author_facet Jang, Seung Hun
Lee, Dong Yoon
Jeong, Jihyeon
Choi, Won-Il
author_sort Jang, Seung Hun
collection PubMed
description BACKGROUND/AIMS: The treatment of epidermal growth factor receptor (EGFR)-mutated lung cancer cases has shown remarkable development in the past two decades. However, there have been limited studies comparing the prognostic effects of EGFR-tyrosine kinase inhibitor (TKI) and other treatment modalities. Therefore, we compared the survival outcomes of patients treated with EGFR-TKIs versus those treated with other treatment modalities. METHODS: Patient data were collected from the Korean National Health Insurance Database, National Health Insurance Service-National Sample Cohort 2002 to 2015, which was released by the Korean National Health Insurance Service in 2015. The lung cancer group included patients (n = 2,003) initially diagnosed with lung cancer between January 2010 and December 2013. The main outcome was all-cause mortality. A Cox proportional hazard regression analysis was used to calculate the relative risk of mortality. RESULTS: Among the newly diagnosed lung cancer cases, 1,004 (50.1%) were included in the analysis. A 15.1-month median survival benefit was observed in the EGFR-TKI group than that of the multimodality therapy group. The risk of mortality was as follows: EGFR-TKI treatment group (n = 142; hazard ratio [HR], 5.29; 95% confidence interval [CI], 3.57 to 7.86) and multimodality therapy group (n = 326; HR, 7.42; 95% CI, 5.19 to 10.63) compared to surgery only (n = 275). CONCLUSIONS: Patients with advanced lung cancer harbouring EGFR mutations treated with EGFR-TKIs showed better median survival and lower risk of mortality than those in the multimodality therapy group. In the case of EGFR-mutated advanced lung cancer, there is room for downstaging in the TNM classification.
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spelling pubmed-92717282022-07-13 Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer Jang, Seung Hun Lee, Dong Yoon Jeong, Jihyeon Choi, Won-Il Korean J Intern Med Original Article BACKGROUND/AIMS: The treatment of epidermal growth factor receptor (EGFR)-mutated lung cancer cases has shown remarkable development in the past two decades. However, there have been limited studies comparing the prognostic effects of EGFR-tyrosine kinase inhibitor (TKI) and other treatment modalities. Therefore, we compared the survival outcomes of patients treated with EGFR-TKIs versus those treated with other treatment modalities. METHODS: Patient data were collected from the Korean National Health Insurance Database, National Health Insurance Service-National Sample Cohort 2002 to 2015, which was released by the Korean National Health Insurance Service in 2015. The lung cancer group included patients (n = 2,003) initially diagnosed with lung cancer between January 2010 and December 2013. The main outcome was all-cause mortality. A Cox proportional hazard regression analysis was used to calculate the relative risk of mortality. RESULTS: Among the newly diagnosed lung cancer cases, 1,004 (50.1%) were included in the analysis. A 15.1-month median survival benefit was observed in the EGFR-TKI group than that of the multimodality therapy group. The risk of mortality was as follows: EGFR-TKI treatment group (n = 142; hazard ratio [HR], 5.29; 95% confidence interval [CI], 3.57 to 7.86) and multimodality therapy group (n = 326; HR, 7.42; 95% CI, 5.19 to 10.63) compared to surgery only (n = 275). CONCLUSIONS: Patients with advanced lung cancer harbouring EGFR mutations treated with EGFR-TKIs showed better median survival and lower risk of mortality than those in the multimodality therapy group. In the case of EGFR-mutated advanced lung cancer, there is room for downstaging in the TNM classification. Korean Association of Internal Medicine 2022-07 2022-06-03 /pmc/articles/PMC9271728/ /pubmed/35811369 http://dx.doi.org/10.3904/kjim.2021.488 Text en Copyright © 2022 The Korean Association of Internal Medicine https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jang, Seung Hun
Lee, Dong Yoon
Jeong, Jihyeon
Choi, Won-Il
Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title_full Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title_fullStr Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title_full_unstemmed Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title_short Prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
title_sort prognostic outcome of treatment modalities for epidermal growth factor receptor-mutated advanced lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271728/
https://www.ncbi.nlm.nih.gov/pubmed/35811369
http://dx.doi.org/10.3904/kjim.2021.488
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