Advanced Progress in Targeted Drugs Therapy for Non-Small Cell Lung Cancer

靶向治疗 肺癌 医学 癌症治疗 肿瘤科 重症监护医学 癌症 内科学
作者
Yuhan Song
出处
期刊: 卷期号:111 (1): 191-199
标识
DOI:10.54254/2753-8818/2025.au23560
摘要

In modern society, cancer is the most therapeutic disease. Among all types of cancer, the highest mortality rate is lung cancer and 85% of lung cancer patients is non-small cell lung cancer (NSCLC). However, significant therapeutic advancesparticularly in targeted therapy and immunotherapyhave revolutionized its treatment landscape. This review systematically summarizes recent progress in these two approaches of targeted therapy and immunotherapy. Regarding targeted therapy, particular emphasis is placed on three key targets: Epidermal Growth Factor Receptor (EGFR), Anaplastic Lymphoma Kinase (ALK), and ROS Proto-Oncogene 1(ROS1). EGFR mutations promote tumorigenesis by activating downstream signaling pathways. Up to the current era, the sequential development of three tyrosine kinase inhibitors (TKI) generations has enabled progressively refined targeting of EGFR-mutated tumorigenesis. ALK gene rearrangement serves as a pivotal oncogenic driver in NSCLC. It activates downstream signaling pathways to promote cancer initiation and progression, with corresponding inhibitors now advancing to the third generation. Due to its high homology with ALK, the ROS1 gene has shown significant responsiveness to some ALK inhibitors. Regarding immunotherapy, the analysis covers three approaches: cancer vaccines, cellular immunotherapy, and immune checkpoint inhibitors. For immunotherapy, we analyze three strategies. Cancer vaccines, which prime tumor-specific immune responses by antigen presentation; Cellular immunotherapies (e.g., Chimeric Antigen Receptor-Modified T Cells (CAR-T), T-Cell Receptor Engineering (TCR-T), and Tumor-Infiltrating Lymphocytes (TIL) therapies), engineered to enhance antitumor immunity. And immune checkpoint inhibitors (e.g., PD-1/PD-L1 blockers), which reinvigorate T-cell function by disrupting immunosuppressive signals. Despite their clinical success, challenges like drug resistance and toxicity persist. Future research should prioritize novel targets, innovative technologies, and combination strategies to further transform NSCLC treatment.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
4秒前
changhao6787发布了新的文献求助10
4秒前
lizishu应助阿辰采纳,获得10
6秒前
syyy完成签到,获得积分10
7秒前
十三完成签到,获得积分10
7秒前
upctyk完成签到,获得积分20
7秒前
任性的傲柏完成签到,获得积分10
7秒前
Nyquist完成签到,获得积分10
7秒前
7秒前
7秒前
FashionBoy应助lagom采纳,获得10
8秒前
tylerconan发布了新的文献求助10
8秒前
9秒前
Cecily发布了新的文献求助10
9秒前
qiqi完成签到,获得积分10
9秒前
9秒前
10秒前
韶绍完成签到 ,获得积分10
10秒前
东北饿霸完成签到,获得积分10
10秒前
10秒前
呀呀呀完成签到,获得积分10
12秒前
12秒前
深情安青应助5999采纳,获得10
13秒前
13秒前
13秒前
威武水绿发布了新的文献求助10
13秒前
skysleeper发布了新的文献求助10
14秒前
YUJIALING发布了新的文献求助10
15秒前
大力的冬萱应助FLL采纳,获得20
16秒前
MingY完成签到,获得积分10
17秒前
在水一方应助长情胡萝卜采纳,获得10
18秒前
kyt完成签到,获得积分10
18秒前
lagom发布了新的文献求助10
18秒前
怕黑明雪完成签到,获得积分10
18秒前
Chemistry发布了新的文献求助10
19秒前
77完成签到,获得积分10
19秒前
刘雯完成签到,获得积分10
20秒前
科研通AI6.3应助青耕采纳,获得10
21秒前
ding应助one采纳,获得10
21秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Organic Chemistry, 5th Edition 1000
Nondestructive Testing Handbook: Vol. 4, Thermal and Infrared Testing (IR), 4th ed 800
作者名:Kristopher P. Plain,悉尼大学的,目前只能查到其四篇论文,想找到其博士论文 590
Évora na Idade Média 555
Soil mites of the family Rhagidiidae (Actinedida: Eupodoidea). Morphology, Systematics, Ecology 520
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7371196
求助须知:如何正确求助?哪些是违规求助? 8978827
关于积分的说明 19088682
捐赠科研通 7013188
什么是DOI,文献DOI怎么找? 3225034
关于科研通互助平台的介绍 2388657
邀请新用户注册赠送积分活动 2205699