Cargando…

Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors

BACKGROUND: Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) readministration to lung cancer patients is common owing to the few options available. Impact of clinical factors on prognosis of EGFR-mutant non-small cell lung cancer (NSCLC) patients receiving EGFR-TKI readministr...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Yu-Mu, Lai, Chien-Hao, Rau, Kun-Ming, Huang, Cheng-Hua, Chang, Huang-Chih, Chao, Tung-Ying, Tseng, Chia-Cheng, Fang, Wen-Feng, Chung, Yu-Hsiu, Wang, Yi-Hsi, Su, Mao-Chang, Huang, Kuo-Tung, Liu, Shih-Feng, Chen, Hung-Chen, Chang, Ya-Chun, Chang, Yu-Ping, Wang, Chin-Chou, Lin, Meng-Chih
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100346/
https://www.ncbi.nlm.nih.gov/pubmed/27821111
http://dx.doi.org/10.1186/s12885-016-2917-6
_version_ 1782466123509268480
author Chen, Yu-Mu
Lai, Chien-Hao
Rau, Kun-Ming
Huang, Cheng-Hua
Chang, Huang-Chih
Chao, Tung-Ying
Tseng, Chia-Cheng
Fang, Wen-Feng
Chung, Yu-Hsiu
Wang, Yi-Hsi
Su, Mao-Chang
Huang, Kuo-Tung
Liu, Shih-Feng
Chen, Hung-Chen
Chang, Ya-Chun
Chang, Yu-Ping
Wang, Chin-Chou
Lin, Meng-Chih
author_facet Chen, Yu-Mu
Lai, Chien-Hao
Rau, Kun-Ming
Huang, Cheng-Hua
Chang, Huang-Chih
Chao, Tung-Ying
Tseng, Chia-Cheng
Fang, Wen-Feng
Chung, Yu-Hsiu
Wang, Yi-Hsi
Su, Mao-Chang
Huang, Kuo-Tung
Liu, Shih-Feng
Chen, Hung-Chen
Chang, Ya-Chun
Chang, Yu-Ping
Wang, Chin-Chou
Lin, Meng-Chih
author_sort Chen, Yu-Mu
collection PubMed
description BACKGROUND: Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) readministration to lung cancer patients is common owing to the few options available. Impact of clinical factors on prognosis of EGFR-mutant non-small cell lung cancer (NSCLC) patients receiving EGFR-TKI readministration after first-line EGFR-TKI failure and a period of TKI holiday remains unclear. Through this retrospective study, we aimed to understand the impact of clinical factors in such patients. METHODS: Of 1386 cases diagnosed between December 2010 and December 2013, 80 EGFR-mutant NSCLC patients who were readministered TKIs after failure of first-line TKIs and intercalated with at least one cycle of cytotoxic agent were included. We evaluated clinical factors that may influence prognosis of TKI readministration as well as systemic inflammatory status in terms of neutrophil-to-lymphocyte ratio (NLR) and lymphocyte-to-monocyte ratio (LMR). Baseline NLR and LMR were estimated at the beginning of TKI readministration and trends of NLR and LMR were change amount from patients receiving first-Line TKIs to TKIs readministration. RESULTS: Median survival time since TKI readministration was 7.0 months. In the univariable analysis, progression free survival (PFS) of first-line TKIs, baseline NLR and LMR, and trend of LMR were prognostic factors in patients receiving TKIs readministration. In the multivariate analysis, only PFS of first-line TKIs (p < 0.001), baseline NLR (p = 0.037), and trend of LMR (p = 0.004) were prognostic factors. CONCLUSION: Longer PFS of first-line TKIs, low baseline NLR, and high trend of LMR were good prognostic factors in EGFR-mutant NSCLC patients receiving TKI readministration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2917-6) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5100346
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-51003462016-11-08 Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors Chen, Yu-Mu Lai, Chien-Hao Rau, Kun-Ming Huang, Cheng-Hua Chang, Huang-Chih Chao, Tung-Ying Tseng, Chia-Cheng Fang, Wen-Feng Chung, Yu-Hsiu Wang, Yi-Hsi Su, Mao-Chang Huang, Kuo-Tung Liu, Shih-Feng Chen, Hung-Chen Chang, Ya-Chun Chang, Yu-Ping Wang, Chin-Chou Lin, Meng-Chih BMC Cancer Research Article BACKGROUND: Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) readministration to lung cancer patients is common owing to the few options available. Impact of clinical factors on prognosis of EGFR-mutant non-small cell lung cancer (NSCLC) patients receiving EGFR-TKI readministration after first-line EGFR-TKI failure and a period of TKI holiday remains unclear. Through this retrospective study, we aimed to understand the impact of clinical factors in such patients. METHODS: Of 1386 cases diagnosed between December 2010 and December 2013, 80 EGFR-mutant NSCLC patients who were readministered TKIs after failure of first-line TKIs and intercalated with at least one cycle of cytotoxic agent were included. We evaluated clinical factors that may influence prognosis of TKI readministration as well as systemic inflammatory status in terms of neutrophil-to-lymphocyte ratio (NLR) and lymphocyte-to-monocyte ratio (LMR). Baseline NLR and LMR were estimated at the beginning of TKI readministration and trends of NLR and LMR were change amount from patients receiving first-Line TKIs to TKIs readministration. RESULTS: Median survival time since TKI readministration was 7.0 months. In the univariable analysis, progression free survival (PFS) of first-line TKIs, baseline NLR and LMR, and trend of LMR were prognostic factors in patients receiving TKIs readministration. In the multivariate analysis, only PFS of first-line TKIs (p < 0.001), baseline NLR (p = 0.037), and trend of LMR (p = 0.004) were prognostic factors. CONCLUSION: Longer PFS of first-line TKIs, low baseline NLR, and high trend of LMR were good prognostic factors in EGFR-mutant NSCLC patients receiving TKI readministration. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2917-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-08 /pmc/articles/PMC5100346/ /pubmed/27821111 http://dx.doi.org/10.1186/s12885-016-2917-6 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chen, Yu-Mu
Lai, Chien-Hao
Rau, Kun-Ming
Huang, Cheng-Hua
Chang, Huang-Chih
Chao, Tung-Ying
Tseng, Chia-Cheng
Fang, Wen-Feng
Chung, Yu-Hsiu
Wang, Yi-Hsi
Su, Mao-Chang
Huang, Kuo-Tung
Liu, Shih-Feng
Chen, Hung-Chen
Chang, Ya-Chun
Chang, Yu-Ping
Wang, Chin-Chou
Lin, Meng-Chih
Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title_full Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title_fullStr Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title_full_unstemmed Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title_short Impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
title_sort impact of clinical parameters and systemic inflammatory status on epidermal growth factor receptor-mutant non-small cell lung cancer patients readministration with epidermal growth factor receptor tyrosine kinase inhibitors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100346/
https://www.ncbi.nlm.nih.gov/pubmed/27821111
http://dx.doi.org/10.1186/s12885-016-2917-6
work_keys_str_mv AT chenyumu impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT laichienhao impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT raukunming impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT huangchenghua impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT changhuangchih impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT chaotungying impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT tsengchiacheng impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT fangwenfeng impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT chungyuhsiu impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT wangyihsi impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT sumaochang impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT huangkuotung impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT liushihfeng impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT chenhungchen impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT changyachun impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT changyuping impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT wangchinchou impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors
AT linmengchih impactofclinicalparametersandsystemicinflammatorystatusonepidermalgrowthfactorreceptormutantnonsmallcelllungcancerpatientsreadministrationwithepidermalgrowthfactorreceptortyrosinekinaseinhibitors