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Combatting acquired resistance to osimertinib in EGFR-mutant lung cancer
The discovery of activating mutations in epidermal growth factor receptor (EGFR) in non-small-cell lung cancer transformed the care and prognosis of patients and heralded the era of ‘personalized medicine’ in thoracic oncology. Osimertinib, a third-generation EGFR inhibitor, has been established as...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761802/ https://www.ncbi.nlm.nih.gov/pubmed/36544540 http://dx.doi.org/10.1177/17588359221144099 |
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author | Lee, Jiyun Piotrowska, Zofia Soo, Ross Cho, Byoung Chul Lim, Sun Min |
author_facet | Lee, Jiyun Piotrowska, Zofia Soo, Ross Cho, Byoung Chul Lim, Sun Min |
author_sort | Lee, Jiyun |
collection | PubMed |
description | The discovery of activating mutations in epidermal growth factor receptor (EGFR) in non-small-cell lung cancer transformed the care and prognosis of patients and heralded the era of ‘personalized medicine’ in thoracic oncology. Osimertinib, a third-generation EGFR inhibitor, has been established as the preferred EGFR inhibitor for newly diagnosed patients which urged the need to develop treatment options for patients progressing on first-line osimertinib. However, acquired resistance invariably emerges and numerous efforts have been attempted to delay or overcome acquired resistance. In this article, we thoroughly reviewed the current understanding of osimertinib resistance mechanisms and explored the established and emerging treatment options. Newer treatment strategies targeting EGFR-dependent or -independent resistance mechanisms, novel approaches using bispecific antibodies and antibody–drug conjugates will be discussed. Moreover, what to do with brain only progression, and how to incorporate immunotherapy in EGFR-mutant lung cancer will be discussed. Lastly, future perspectives on the ongoing clinical trials and combination of front-line therapy will be introduced. |
format | Online Article Text |
id | pubmed-9761802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-97618022022-12-20 Combatting acquired resistance to osimertinib in EGFR-mutant lung cancer Lee, Jiyun Piotrowska, Zofia Soo, Ross Cho, Byoung Chul Lim, Sun Min Ther Adv Med Oncol Review The discovery of activating mutations in epidermal growth factor receptor (EGFR) in non-small-cell lung cancer transformed the care and prognosis of patients and heralded the era of ‘personalized medicine’ in thoracic oncology. Osimertinib, a third-generation EGFR inhibitor, has been established as the preferred EGFR inhibitor for newly diagnosed patients which urged the need to develop treatment options for patients progressing on first-line osimertinib. However, acquired resistance invariably emerges and numerous efforts have been attempted to delay or overcome acquired resistance. In this article, we thoroughly reviewed the current understanding of osimertinib resistance mechanisms and explored the established and emerging treatment options. Newer treatment strategies targeting EGFR-dependent or -independent resistance mechanisms, novel approaches using bispecific antibodies and antibody–drug conjugates will be discussed. Moreover, what to do with brain only progression, and how to incorporate immunotherapy in EGFR-mutant lung cancer will be discussed. Lastly, future perspectives on the ongoing clinical trials and combination of front-line therapy will be introduced. SAGE Publications 2022-12-17 /pmc/articles/PMC9761802/ /pubmed/36544540 http://dx.doi.org/10.1177/17588359221144099 Text en © The Author(s), 2022. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Lee, Jiyun Piotrowska, Zofia Soo, Ross Cho, Byoung Chul Lim, Sun Min Combatting acquired resistance to osimertinib in EGFR-mutant lung cancer |
title | Combatting acquired resistance to osimertinib in EGFR-mutant lung
cancer |
title_full | Combatting acquired resistance to osimertinib in EGFR-mutant lung
cancer |
title_fullStr | Combatting acquired resistance to osimertinib in EGFR-mutant lung
cancer |
title_full_unstemmed | Combatting acquired resistance to osimertinib in EGFR-mutant lung
cancer |
title_short | Combatting acquired resistance to osimertinib in EGFR-mutant lung
cancer |
title_sort | combatting acquired resistance to osimertinib in egfr-mutant lung
cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9761802/ https://www.ncbi.nlm.nih.gov/pubmed/36544540 http://dx.doi.org/10.1177/17588359221144099 |
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