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EGFR外显子20插入突变型NSCLC治疗的研究进展

Lung cancer has become one of the most dangerous cancers to human health and the mortality rate is the highest among all the causes of cancer death. Non-small cell lung cancer (NSCLC) accounts for about 80%-85% of lung cancer. Chemotherapy is the main treatment for advanced NSCLC, but the 5-year sur...

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Autores principales: XU, Meiyi, LUO, Jiawei, XU, Ruilian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial board of Chinese Journal of Lung Cancer 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033241/
https://www.ncbi.nlm.nih.gov/pubmed/36872053
http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.05
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author XU, Meiyi
LUO, Jiawei
XU, Ruilian
author_facet XU, Meiyi
LUO, Jiawei
XU, Ruilian
author_sort XU, Meiyi
collection PubMed
description Lung cancer has become one of the most dangerous cancers to human health and the mortality rate is the highest among all the causes of cancer death. Non-small cell lung cancer (NSCLC) accounts for about 80%-85% of lung cancer. Chemotherapy is the main treatment for advanced NSCLC, but the 5-year survival rate is low. Epidermal growth factor receptor (EGFR) mutations are the most common driver mutations in lung cancer, but EGFR exon 20 insertions (EGFR ex20ins) mutation belongs to one of the rare mutations, accounting for about 4%-10% of overall EGFR mutations, thus around 1.8% of advanced NSCLC patients. In recent years, targeted therapies represented by EGFR tyrosine kinase inhibitors (TKIs) have become an important treatment option for patients with advanced NSCLC, however, NSCLC patients with EGFR ex20ins mutation are not sensitive to most of EGFR-TKIs treatments. Currently, some of the targeted drugs for EGFR ex20ins mutation have achieved significant efficacy, while some of them are still under clinical investigation. In this article, we will describe various treatment methods for EGFR ex20ins mutation and their efficacy.
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spelling pubmed-100332412023-03-24 EGFR外显子20插入突变型NSCLC治疗的研究进展 XU, Meiyi LUO, Jiawei XU, Ruilian Zhongguo Fei Ai Za Zhi Review Lung cancer has become one of the most dangerous cancers to human health and the mortality rate is the highest among all the causes of cancer death. Non-small cell lung cancer (NSCLC) accounts for about 80%-85% of lung cancer. Chemotherapy is the main treatment for advanced NSCLC, but the 5-year survival rate is low. Epidermal growth factor receptor (EGFR) mutations are the most common driver mutations in lung cancer, but EGFR exon 20 insertions (EGFR ex20ins) mutation belongs to one of the rare mutations, accounting for about 4%-10% of overall EGFR mutations, thus around 1.8% of advanced NSCLC patients. In recent years, targeted therapies represented by EGFR tyrosine kinase inhibitors (TKIs) have become an important treatment option for patients with advanced NSCLC, however, NSCLC patients with EGFR ex20ins mutation are not sensitive to most of EGFR-TKIs treatments. Currently, some of the targeted drugs for EGFR ex20ins mutation have achieved significant efficacy, while some of them are still under clinical investigation. In this article, we will describe various treatment methods for EGFR ex20ins mutation and their efficacy. Editorial board of Chinese Journal of Lung Cancer 2023-02-20 /pmc/articles/PMC10033241/ /pubmed/36872053 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.05 Text en https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/.
spellingShingle Review
XU, Meiyi
LUO, Jiawei
XU, Ruilian
EGFR外显子20插入突变型NSCLC治疗的研究进展
title EGFR外显子20插入突变型NSCLC治疗的研究进展
title_full EGFR外显子20插入突变型NSCLC治疗的研究进展
title_fullStr EGFR外显子20插入突变型NSCLC治疗的研究进展
title_full_unstemmed EGFR外显子20插入突变型NSCLC治疗的研究进展
title_short EGFR外显子20插入突变型NSCLC治疗的研究进展
title_sort egfr外显子20插入突变型nsclc治疗的研究进展
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10033241/
https://www.ncbi.nlm.nih.gov/pubmed/36872053
http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.05
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