Efficacy of immunotherapy in oncogene-driven non-small-cell lung cancer

被引:17
|
作者
Vokes, Natalie I. [2 ,3 ]
Pan, Kelsey [4 ]
Le, Xiuning [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, 1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Genom Med, Houston, TX USA
[4] Univ Texas MD Anderson Canc Ctr, Dept Canc Med, Houston, TX USA
关键词
immunotherapy; lung cancer; precision oncology; oncogene; COOCCURRING GENOMIC ALTERATIONS; EGFR-MUTANT NSCLC; DEATH-LIGAND; 1ST-LINE TREATMENT; PD-L1; EXPRESSION; IMMUNE ESCAPE; CHECKPOINT INHIBITORS; CLINICAL-RESPONSE; NEVER SMOKERS; OPEN-LABEL;
D O I
10.1177/17588359231161409
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For advanced metastatic non-small-lung cancer, the landscape of actionable driver alterations is rapidly growing, with nine targetable oncogenes and seven approvals within the last 5 years. This accelerated drug development has expanded the reach of targeted therapies, and it may soon be that a majority of patients with lung adenocarcinoma will be eligible for a targeted therapy during their treatment course. With these emerging therapeutic options, it is important to understand the existing data on immune checkpoint inhibitors (ICIs), along with their efficacy and safety for each oncogene-driven lung cancer, to best guide the selection and sequencing of various therapeutic options. This article reviews the clinical data on ICIs for each of the driver oncogene defined lung cancer subtypes, including efficacy, both for ICI as monotherapy or in combination with chemotherapy or radiation; toxicities from ICI/targeted therapy in combination or in sequence; and potential strategies to enhance ICI efficacy in oncogene-driven non-small-cell lung cancers.
引用
收藏
页数:20
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