egfr突变非小细胞肺癌患者的个性化护理:早期到晚期疾病管理导航

IF 503.1 1区 医学 Q1 ONCOLOGY
Maxime Borgeaud,Timothée Olivier,Jair Bar,Stephanie Pei Li Saw,Kaushal Parikh,Giuseppe Luigi Banna,Claudio De Vito,Jill Feldman,Xiuning Le,Alfredo Addeo
{"title":"egfr突变非小细胞肺癌患者的个性化护理:早期到晚期疾病管理导航","authors":"Maxime Borgeaud,Timothée Olivier,Jair Bar,Stephanie Pei Li Saw,Kaushal Parikh,Giuseppe Luigi Banna,Claudio De Vito,Jill Feldman,Xiuning Le,Alfredo Addeo","doi":"10.3322/caac.70024","DOIUrl":null,"url":null,"abstract":"The discovery of activating mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the management of lung cancer, enabling the development of targeted tyrosine kinase inhibitors (TKIs). These therapies offer improved survival and reduced side effects compared with conventional treatments. Recent advancements have significantly reshaped the treatment paradigm for EGFR-mutant non-small cell lung cancer. TKIs are now incorporated into the management of early stage and locally advanced disease, and phase 3 trials have explored combination strategies in metastatic settings. Although these intensified approaches improve progression-free survival, they come with increased toxicity and higher costs, underscoring the need for precise patient selection to maximize benefit. Emerging data on biomarkers, such as co-mutations and circulating tumor DNA, show promise for refining treatment decisions. In addition, significant progress in understanding resistance mechanisms to EGFR TKIs has broadened therapeutic options. This review provides a comprehensive overview of the current landscape of EGFR-mutant nonsmall cell lung cancer, highlighting recent breakthroughs and discussing strategies to optimize treatment based on the latest evidence.","PeriodicalId":137,"journal":{"name":"CA: A Cancer Journal for Clinicians","volume":"13 1","pages":""},"PeriodicalIF":503.1000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Personalized care for patients with EGFR-mutant nonsmall cell lung cancer: Navigating early to advanced disease management.\",\"authors\":\"Maxime Borgeaud,Timothée Olivier,Jair Bar,Stephanie Pei Li Saw,Kaushal Parikh,Giuseppe Luigi Banna,Claudio De Vito,Jill Feldman,Xiuning Le,Alfredo Addeo\",\"doi\":\"10.3322/caac.70024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The discovery of activating mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the management of lung cancer, enabling the development of targeted tyrosine kinase inhibitors (TKIs). These therapies offer improved survival and reduced side effects compared with conventional treatments. Recent advancements have significantly reshaped the treatment paradigm for EGFR-mutant non-small cell lung cancer. TKIs are now incorporated into the management of early stage and locally advanced disease, and phase 3 trials have explored combination strategies in metastatic settings. Although these intensified approaches improve progression-free survival, they come with increased toxicity and higher costs, underscoring the need for precise patient selection to maximize benefit. Emerging data on biomarkers, such as co-mutations and circulating tumor DNA, show promise for refining treatment decisions. In addition, significant progress in understanding resistance mechanisms to EGFR TKIs has broadened therapeutic options. This review provides a comprehensive overview of the current landscape of EGFR-mutant nonsmall cell lung cancer, highlighting recent breakthroughs and discussing strategies to optimize treatment based on the latest evidence.\",\"PeriodicalId\":137,\"journal\":{\"name\":\"CA: A Cancer Journal for Clinicians\",\"volume\":\"13 1\",\"pages\":\"\"},\"PeriodicalIF\":503.1000,\"publicationDate\":\"2025-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"CA: A Cancer Journal for Clinicians\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3322/caac.70024\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"CA: A Cancer Journal for Clinicians","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3322/caac.70024","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

表皮生长因子受体(EGFR)基因激活突变的发现彻底改变了肺癌的治疗,使靶向酪氨酸激酶抑制剂(TKIs)的开发成为可能。与传统疗法相比,这些疗法提高了生存率,减少了副作用。最近的进展显著地重塑了egfr突变的非小细胞肺癌的治疗模式。TKIs现在被纳入早期和局部晚期疾病的治疗中,3期试验探索了转移性疾病的联合治疗策略。虽然这些强化的方法提高了无进展生存期,但它们的毒性增加,成本更高,强调了精确选择患者以最大化获益的必要性。关于生物标志物的新数据,如共突变和循环肿瘤DNA,显示出改进治疗决策的希望。此外,对EGFR TKIs耐药机制的理解取得了重大进展,拓宽了治疗选择。本文综述了egfr突变型非小细胞肺癌的现状,重点介绍了最近的突破,并讨论了基于最新证据的优化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Personalized care for patients with EGFR-mutant nonsmall cell lung cancer: Navigating early to advanced disease management.
The discovery of activating mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the management of lung cancer, enabling the development of targeted tyrosine kinase inhibitors (TKIs). These therapies offer improved survival and reduced side effects compared with conventional treatments. Recent advancements have significantly reshaped the treatment paradigm for EGFR-mutant non-small cell lung cancer. TKIs are now incorporated into the management of early stage and locally advanced disease, and phase 3 trials have explored combination strategies in metastatic settings. Although these intensified approaches improve progression-free survival, they come with increased toxicity and higher costs, underscoring the need for precise patient selection to maximize benefit. Emerging data on biomarkers, such as co-mutations and circulating tumor DNA, show promise for refining treatment decisions. In addition, significant progress in understanding resistance mechanisms to EGFR TKIs has broadened therapeutic options. This review provides a comprehensive overview of the current landscape of EGFR-mutant nonsmall cell lung cancer, highlighting recent breakthroughs and discussing strategies to optimize treatment based on the latest evidence.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
873.20
自引率
0.10%
发文量
51
审稿时长
1 months
期刊介绍: CA: A Cancer Journal for Clinicians" has been published by the American Cancer Society since 1950, making it one of the oldest peer-reviewed journals in oncology. It maintains the highest impact factor among all ISI-ranked journals. The journal effectively reaches a broad and diverse audience of health professionals, offering a unique platform to disseminate information on cancer prevention, early detection, various treatment modalities, palliative care, advocacy matters, quality-of-life topics, and more. As the premier journal of the American Cancer Society, it publishes mission-driven content that significantly influences patient care.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信