Oncogenic fusions: Targeting NTRK

被引:5
|
作者
Hagopian, Garo [1 ]
Nagasaka, Misako [1 ,2 ,3 ]
机构
[1] Univ Calif Irvine, Med Ctr, Dept Med, Orange, CA 92868 USA
[2] St Marianna Univ, Sch Med, Dept Med, Kawasaki, Japan
[3] Univ Calif Irvine, Sch Med, 101 City Dr, Orange, CA 92868 USA
关键词
Neurotrophic tyrosine receptor kinase; Entrectinib; Larotrectinib; Repotrectinib; TRK related adverse events; POSITIVE SOLID TUMORS; ACQUIRED-RESISTANCE; TRK INHIBITOR; KINASE; LAROTRECTINIB; ENTRECTINIB; EFFICACY; NEUROTROPHIN; TROPOMYOSIN; RECEPTORS;
D O I
10.1016/j.critrevonc.2023.104234
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Non-Small Cell Lung Cancer (NSCLC) is responsible for the highest number of cancer-related deaths in the United States. Thankfully, advancements in the detection and targeting of gene mutations have greatly improved outcomes for many patients. One significant mutation driving oncogenesis in various cancers, including NSCLC, is the neurotrophic tyrosine receptor kinase (NTRK) fusion. Presently, larotrectinib and entrectinib are the only FDA-approved therapies for NTRK-mutated cancers. Despite the efficacy and tolerability exhibited by these therapies, several clinical hurdles persist for physicians, including resistance mutations and limited penetration of the central nervous system (CNS), which diminishes their effectiveness. The treatment landscape for NTRK cancers is still being explored, with numerous new tyrosine kinase inhibitors currently in development or undergoing phase 1 and 2 clinical trials. In this review, we delve into both established and novel therapies targeting NTRK-mutated NSCLC.
引用
收藏
页数:8
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