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Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study

Lung cancer remains the primary cause of cancer-related mortality worldwide. Several treatment modalities are available for lung cancer, including surgery, radiation, and chemotherapy. Among the chemotherapeutics available, afatinib has been shown to be effective for those with epidermal growth fact...

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Autores principales: Liang, Sheng-Kai, Lee, Meng-Rui, Liao, Wei-Yu, Ho, Chao-Chi, Ko, Jen-Chung, Shih, Jin-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955108/
https://www.ncbi.nlm.nih.gov/pubmed/29805772
http://dx.doi.org/10.18632/oncotarget.25255
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author Liang, Sheng-Kai
Lee, Meng-Rui
Liao, Wei-Yu
Ho, Chao-Chi
Ko, Jen-Chung
Shih, Jin-Yuan
author_facet Liang, Sheng-Kai
Lee, Meng-Rui
Liao, Wei-Yu
Ho, Chao-Chi
Ko, Jen-Chung
Shih, Jin-Yuan
author_sort Liang, Sheng-Kai
collection PubMed
description Lung cancer remains the primary cause of cancer-related mortality worldwide. Several treatment modalities are available for lung cancer, including surgery, radiation, and chemotherapy. Among the chemotherapeutics available, afatinib has been shown to be effective for those with epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma. Herein, we analyzed the factors affecting the prognosis of patients who received afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma in the real-world setting. Patients who received afatinib as a first-line therapy and were reimbursed by the National Health Insurance were recruited in this study. Data on patient characteristics and treatment courses were collected. In total, 259 patients were enrolled (median follow-up, 22.0 months). Of them, 82 (31.7%) were identified to have brain metastases at baseline, which were associated with poor Eastern Cooperative Oncology Group performance status, high incidence of central nervous system progression, and short overall survival. However, the results of our analysis showed that overall survival was not affected by reductions in the afatinib dosage or any upfront local treatments for brain tumors. Multivariate analyses showed that brain metastases at diagnosis and treatment response to afatinib are two important prognostic factors for the overall survival of patients with EGFR mutation-positive lung adenocarcinoma.
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spelling pubmed-59551082018-05-27 Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study Liang, Sheng-Kai Lee, Meng-Rui Liao, Wei-Yu Ho, Chao-Chi Ko, Jen-Chung Shih, Jin-Yuan Oncotarget Clinical Research Paper Lung cancer remains the primary cause of cancer-related mortality worldwide. Several treatment modalities are available for lung cancer, including surgery, radiation, and chemotherapy. Among the chemotherapeutics available, afatinib has been shown to be effective for those with epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma. Herein, we analyzed the factors affecting the prognosis of patients who received afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma in the real-world setting. Patients who received afatinib as a first-line therapy and were reimbursed by the National Health Insurance were recruited in this study. Data on patient characteristics and treatment courses were collected. In total, 259 patients were enrolled (median follow-up, 22.0 months). Of them, 82 (31.7%) were identified to have brain metastases at baseline, which were associated with poor Eastern Cooperative Oncology Group performance status, high incidence of central nervous system progression, and short overall survival. However, the results of our analysis showed that overall survival was not affected by reductions in the afatinib dosage or any upfront local treatments for brain tumors. Multivariate analyses showed that brain metastases at diagnosis and treatment response to afatinib are two important prognostic factors for the overall survival of patients with EGFR mutation-positive lung adenocarcinoma. Impact Journals LLC 2018-05-04 /pmc/articles/PMC5955108/ /pubmed/29805772 http://dx.doi.org/10.18632/oncotarget.25255 Text en Copyright: © 2018 Liang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Clinical Research Paper
Liang, Sheng-Kai
Lee, Meng-Rui
Liao, Wei-Yu
Ho, Chao-Chi
Ko, Jen-Chung
Shih, Jin-Yuan
Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title_full Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title_fullStr Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title_full_unstemmed Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title_short Prognostic factors of afatinib as a first-line therapy for advanced EGFR mutation-positive lung adenocarcinoma: a real-world, large cohort study
title_sort prognostic factors of afatinib as a first-line therapy for advanced egfr mutation-positive lung adenocarcinoma: a real-world, large cohort study
topic Clinical Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955108/
https://www.ncbi.nlm.nih.gov/pubmed/29805772
http://dx.doi.org/10.18632/oncotarget.25255
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