Treatment of advanced non-small cell lung cancer with driver mutations: current applications and future directions

被引:13
|
作者
Zhong, Jia [1 ]
Bai, Hua [1 ]
Wang, Zhijie [1 ]
Duan, Jianchun [1 ]
Zhuang, Wei [1 ]
Wang, Di [1 ]
Wan, Rui [1 ]
Xu, Jiachen [1 ]
Fei, Kailun [1 ]
Ma, Zixiao [1 ]
Zhang, Xue [1 ]
Wang, Jie [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Canc Hosp, State Key Lab Mol Oncol, Natl Canc Ctr,Dept Med Oncol,Natl Clin Res Ctr Can, Beijing 100021, Peoples R China
基金
北京市自然科学基金;
关键词
non-small cell lung cancer; driver mutations; treatment strategy; resistant mechanism; immune-checkpoint inhibitors; TYROSINE KINASE INHIBITORS; CIRCULATING TUMOR DNA; BRAF V600E MUTATION; ACQUIRED-RESISTANCE; EGFR-MUTANT; PHASE-II; MOLECULAR CHARACTERIZATION; OLIGOPROGRESSIVE DISEASE; CLINICAL-OUTCOMES; ALK INHIBITORS;
D O I
10.1007/s11684-022-0976-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
With the improved understanding of driver mutations in non-small cell lung cancer (NSCLC), expanding the targeted therapeutic options improved the survival and safety. However, responses to these agents are commonly temporary and incomplete. Moreover, even patients with the same oncogenic driver gene can respond diversely to the same agent. Furthermore, the therapeutic role of immune-checkpoint inhibitors (ICIs) in oncogene-driven NSCLC remains unclear. Therefore, this review aimed to classify the management of NSCLC with driver mutations based on the gene subtype, concomitant mutation, and dynamic alternation. Then, we provide an overview of the resistant mechanism of target therapy occurring in targeted alternations ("target-dependent resistance") and in the parallel and downstream pathways ("target-independent resistance"). Thirdly, we discuss the effectiveness of ICIs for NSCLC with driver mutations and the combined therapeutic approaches that might reverse the immunosuppressive tumor immune microenvironment. Finally, we listed the emerging treatment strategies for the new oncogenic alternations, and proposed the perspective of NSCLC with driver mutations. This review will guide clinicians to design tailored treatments for NSCLC with driver mutations.
引用
收藏
页码:18 / 42
页数:25
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