The trial was a randomized, open-label, multicenter Phase II study of patients with advanced or metastatic NSCLC who don't harbor driver genes. The aim is to explore the efficacy and safety of Envafolimab Combined With Endostar/S-1 in second-line treatment of advanced non-small cell lung cancer.
Patients with advanced (stage IV. NSCLC), after signing informed consent, are screened to meet the admission requirements. All the candidates are not randomly placed in 3 treatment groups (which treatment regimen the patient chooses is determined by the clinical supervisor on a patient-by-case basis).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
45
Immunotherapy combined with chemotherapy and anti VEGFR therapy
Immunotherapy combined with anti VEGFR therapy
Immunotherapy combined with chemotherapy
objective response rate(ORR)
proportion of patients with a complete response or partial response to treatment according to Response Evaluation Criteria in Solid Tumors
Time frame: six weeks
Adverse events
safety
Time frame: three weeks
progression-free survival(PFS)
the time from initial treatment to disease progression
Time frame: six weeks
overall survival(OS)
the time from initial treatment to death from any cause
Time frame: six weeks
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