Novel systemic therapies in the management of tyrosine kinase inhibitor-pretreated patients with epidermal growth factor receptor-mutant non-small-cell lung cancer

被引:3
|
作者
Li, Yang-Si [1 ,2 ]
Jie, Guang-Ling [1 ,2 ]
Wu, Yi-Long [1 ,2 ]
机构
[1] South China Univ Technol, Sch Med, Guangzhou, Peoples R China
[2] Southern Med Univ, Guangdong Lung Canc Inst, Guangdong Acad Med Sci, Guangdong Prov Key Lab Translat Med Lung Canc,Guan, Guangzhou, Peoples R China
关键词
EGFR; non-small-cell lung cancer; novel systemic therapy; pretreatment; targeted therapy; OPEN-LABEL; EGFR-MUTATION; PHASE-III; 1ST-LINE TREATMENT; MET INHIBITOR; LEPTOMENINGEAL METASTASES; ACQUIRED-RESISTANCE; PLUS CHEMOTHERAPY; GEFITINIB; OSIMERTINIB;
D O I
10.1177/17588359231193726
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are the standard first-line option for non-small-cell lung cancer (NSCLC) harboring active EGFR mutations. The overall survival of patients with advanced NSCLC has improved dramatically with the development of comprehensive genetic profiles and targeted therapies. However, resistance inevitably occurs, leading to disease progression after approximately 10-18 months of EGFR-TKI treatment. Platinum-based chemotherapy is the standard treatment for patients who have experienced disease progression while undergoing EGFR-TKI treatment, but its efficacy is limited. The management of extensively pretreated patients with EGFR-mutant NSCLC is becoming increasingly concerning. New agents have shown encouraging efficacy in clinical trials for this patient population, including fourth-generation EGFR-TKIs, EGFR-TKIs combined with counterpart targeted drugs, and novel agents such as antibody-drug conjugates. We review current efforts to manage extensively pretreated patients with EGFR-mutant NSCLC.
引用
收藏
页数:21
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