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Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer

The identification of mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the treatment strategy for non-small cell lung cancer (NSCLC). The effectiveness of individualized treatment using EGFR tyrosine kinase inhibitors (TKIs) for EGFR-mutated NSCLC has mainly been clar...

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Autor principal: INOUE, Akira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443375/
https://www.ncbi.nlm.nih.gov/pubmed/32788550
http://dx.doi.org/10.2183/pjab.96.020
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author INOUE, Akira
author_facet INOUE, Akira
author_sort INOUE, Akira
collection PubMed
description The identification of mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the treatment strategy for non-small cell lung cancer (NSCLC). The effectiveness of individualized treatment using EGFR tyrosine kinase inhibitors (TKIs) for EGFR-mutated NSCLC has mainly been clarified in clinical trials within Japan, and EGFR-TKI monotherapy has been established as the standard first-line treatment for EGFR-mutated NSCLC. Since then, combination regimens involving EGFR-TKI and chemotherapy or anti-angiogenic agents have been developed. Regarding combinations, the NEJ009 study conducted in Japan showed a significant prolongation of progression-free survival and overall survival compared with gefitinib alone. The NEJ009 regimen may be a reasonable option for patients with good performance status in terms of risk–benefit balance. However, further investigation is warranted to improve clinical outcomes in EGFR-mutated NSCLC.
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spelling pubmed-74433752020-08-26 Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer INOUE, Akira Proc Jpn Acad Ser B Phys Biol Sci Review The identification of mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the treatment strategy for non-small cell lung cancer (NSCLC). The effectiveness of individualized treatment using EGFR tyrosine kinase inhibitors (TKIs) for EGFR-mutated NSCLC has mainly been clarified in clinical trials within Japan, and EGFR-TKI monotherapy has been established as the standard first-line treatment for EGFR-mutated NSCLC. Since then, combination regimens involving EGFR-TKI and chemotherapy or anti-angiogenic agents have been developed. Regarding combinations, the NEJ009 study conducted in Japan showed a significant prolongation of progression-free survival and overall survival compared with gefitinib alone. The NEJ009 regimen may be a reasonable option for patients with good performance status in terms of risk–benefit balance. However, further investigation is warranted to improve clinical outcomes in EGFR-mutated NSCLC. The Japan Academy 2020-07-31 /pmc/articles/PMC7443375/ /pubmed/32788550 http://dx.doi.org/10.2183/pjab.96.020 Text en © 2020 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
INOUE, Akira
Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title_full Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title_fullStr Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title_full_unstemmed Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title_short Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer
title_sort progress in individualized treatment for egfr-mutated advanced non-small cell lung cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7443375/
https://www.ncbi.nlm.nih.gov/pubmed/32788550
http://dx.doi.org/10.2183/pjab.96.020
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