Targeted therapy for rare lung cancers: Status, challenges, and prospects

被引:7
|
作者
Wang, Chunsen [1 ]
Yuan, Xiang [1 ]
Xue, Jianxin [1 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Natl Clin Res Ctr Geriatr,Div Thorac Tumor Multimo, Chengdu, Sichuan, Peoples R China
关键词
PULMONARY SARCOMATOID CARCINOMA; LYMPHOEPITHELIOMA-LIKE CARCINOMA; LARGE-CELL CARCINOMA; GLAND-TYPE TUMORS; 14 SKIPPING MUTATION; NF-KAPPA-B; ADENOSQUAMOUS CARCINOMA; NEXT-GENERATION; PD-L1; EXPRESSION; CLINICAL-SIGNIFICANCE;
D O I
10.1016/j.ymthe.2023.05.007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Lung cancer causes the most cancer-related deaths worldwide. In recent years, molecular and immunohistochemical techniques have rapidly developed, further inaugurating an era of personalized medicine for lung cancer. The rare subset of lung cancers accounts for approximately 10%, each displaying distinct clinical characteristics. Treatments for rare lung cancers are mainly based on evidence from common counterparts, which may lead to unsolid clinical benefits considering intertumoral heterogeneity. The increasing knowledge of molecular profiling of rare lung cancers has made targeting genetic alterations and immune checkpoints a powerful strategy. Additionally, cellular therapy has emerged as a promising way to target tumor cells. In this review, we first discuss the current status of targeted therapy and preclinical models for rare lung cancers, as well as provide mutational profiles by integrating the results of existing cohorts. Finally, we point out the challenges and future directions for developing targeted agents for rare lung cancer.
引用
收藏
页码:1960 / 1978
页数:19
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