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Third generation EGFR TKIs: current data and future directions
Acquired T790 M mutation is the commonest cause of resistance for advanced non-small cell lung cancer (NSCLC) epidermal growth factor receptor (EGFR) mutant patients who had progressed after first line EGFR TKI (tyrosine kinase inhibitor). Several third generation EGFR TKIs which are EGFR mutant sel...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817792/ https://www.ncbi.nlm.nih.gov/pubmed/29455654 http://dx.doi.org/10.1186/s12943-018-0778-0 |
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author | Tan, Chee-Seng Kumarakulasinghe, Nesaretnam Barr Huang, Yi-Qing Ang, Yvonne Li En Choo, Joan Rou-En Goh, Boon-Cher Soo, Ross A. |
author_facet | Tan, Chee-Seng Kumarakulasinghe, Nesaretnam Barr Huang, Yi-Qing Ang, Yvonne Li En Choo, Joan Rou-En Goh, Boon-Cher Soo, Ross A. |
author_sort | Tan, Chee-Seng |
collection | PubMed |
description | Acquired T790 M mutation is the commonest cause of resistance for advanced non-small cell lung cancer (NSCLC) epidermal growth factor receptor (EGFR) mutant patients who had progressed after first line EGFR TKI (tyrosine kinase inhibitor). Several third generation EGFR TKIs which are EGFR mutant selective and wild-type (WT) sparing were developed to treat these patients with T790 M acquired resistant mutation. Osimertinib is one of the third generation EGFR TKIs and is currently the most advanced in clinical development. Unfortunately, despite good initial response, patients who was treated with third generation EGFR TKI would develop acquired resistance and several mechanisms had been identified and the commonest being C797S mutation at exon 20. Several novel treatment options were being developed for patients who had progressed on third generation EGFR TKI but they are still in the early phase of development. Osimertinib under FLAURA study had been shown to have better progression-free survival over first generation EGFR TKI in the first line setting and likely will become the new standard of care. |
format | Online Article Text |
id | pubmed-5817792 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58177922018-02-23 Third generation EGFR TKIs: current data and future directions Tan, Chee-Seng Kumarakulasinghe, Nesaretnam Barr Huang, Yi-Qing Ang, Yvonne Li En Choo, Joan Rou-En Goh, Boon-Cher Soo, Ross A. Mol Cancer Review Acquired T790 M mutation is the commonest cause of resistance for advanced non-small cell lung cancer (NSCLC) epidermal growth factor receptor (EGFR) mutant patients who had progressed after first line EGFR TKI (tyrosine kinase inhibitor). Several third generation EGFR TKIs which are EGFR mutant selective and wild-type (WT) sparing were developed to treat these patients with T790 M acquired resistant mutation. Osimertinib is one of the third generation EGFR TKIs and is currently the most advanced in clinical development. Unfortunately, despite good initial response, patients who was treated with third generation EGFR TKI would develop acquired resistance and several mechanisms had been identified and the commonest being C797S mutation at exon 20. Several novel treatment options were being developed for patients who had progressed on third generation EGFR TKI but they are still in the early phase of development. Osimertinib under FLAURA study had been shown to have better progression-free survival over first generation EGFR TKI in the first line setting and likely will become the new standard of care. BioMed Central 2018-02-19 /pmc/articles/PMC5817792/ /pubmed/29455654 http://dx.doi.org/10.1186/s12943-018-0778-0 Text en © The Author(s). 2018 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 | Review Tan, Chee-Seng Kumarakulasinghe, Nesaretnam Barr Huang, Yi-Qing Ang, Yvonne Li En Choo, Joan Rou-En Goh, Boon-Cher Soo, Ross A. Third generation EGFR TKIs: current data and future directions |
title | Third generation EGFR TKIs: current data and future directions |
title_full | Third generation EGFR TKIs: current data and future directions |
title_fullStr | Third generation EGFR TKIs: current data and future directions |
title_full_unstemmed | Third generation EGFR TKIs: current data and future directions |
title_short | Third generation EGFR TKIs: current data and future directions |
title_sort | third generation egfr tkis: current data and future directions |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5817792/ https://www.ncbi.nlm.nih.gov/pubmed/29455654 http://dx.doi.org/10.1186/s12943-018-0778-0 |
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