has been developed as a chemotherapy drug. Many clinical trials with EGFR-TKIs as third line
second line and first line treatment for lung cancer patients were carried out. Only EGFR gene mutations could predict benefit from EGFR-TKIs treatment for patients with lung cancer. Based on the experiences from the development of EGFR-TKIs
Crizotinib (Xalkori
Pfizer) is quickly approved for treatment in some patients with non-small cell lung carcinoma (NSCLC) harboring ALK gene rearrangement in every line. We believe that many other target drugs would be used in clinical practice to treat lung cancer patients. Identification of driver mutations in tumor specimens from Chinese patients is very important. Basic research and drug development in China will be promoted from the discovery of new driver mutations
especially in squamous cell lung cancer and small cell lung cancer. Based on the results of driver mutations tests
Chinese patients will be benefited from global research findings.
DBNLS232 regulates formation of filopodia and promotes cell migration in A549 cells
Efficacy and resistance of EGFR-TKIs for first-line treatment for compound EGFR mutations positive non-small cell lung cancer
Genome-wide screening of tumor suppressor genes in oncogenic transformation of normal lung epithelial cells and preliminary validation in sample databases
Differences in CT findings between solid solitary mucinous lung invasive adenocarcinoma and non-mucinous lung invasive adenocarcinoma
Related Author
YANG Taotao
WANG Xianqi
CHEN Cancan
YAN Wanying
WANG Dawei
XIONG Kunlin
SUN Zhiyuan
CHEN Wei
Related Institution
Department of Oncology, Xinqiao Hospital, Third Military Medical University
Second Department of Respiratory Medicine, First Affiliated Hospital of Luzhou Medical College