This is an interventional study to explore the efficacy and safety of denosumab combined chemotherapy and anti-PD-1/PD-L1 inhibitor in locally advanced or metastatic NSCLC.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
120mg of denosumab,d1 in a 28-days cycle;200mg of anti-PD-1 inhibitor, d1 in a 21-days cycle;500mg/m2 of pemetrexed, d1 in a 21-days cycle; AUC4-5 of carboplatin, d1 in a 21-days cycle, for 4-6 cycle
The First Affiliated Hospital of China Medical University
Shenyang, Liaoning, China
RECRUITING6-month PFS rate
6-month progression-free rate
Time frame: 6 months
progression-free survival(PFS)
Time frame: 24 months
overall survival (OS)
Time frame: 24 months
objective response rate (ORR)
Time frame: 6 months
disease control rate (DCR)
Time frame: 6 months
Number of participants with treatment-related adverse events as assessed by CTCAE v4.0
Time frame: 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.