The purpose of this study is to evaluate the efficacy and safety of Serplulimab Plus Bevacizumab and chemotherapy in TKI-resistant EGFR-mutated non-squamous NSCLC Chinese patients.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
46
Henan Cancer Hospital
Zhengzhou, Henan, China
RECRUITINGORR(Overall Response Rate)
The proportion of subjects who have a complete response (CR) or a partial response (PR)
Time frame: From start of treatment to 12 months
PFS(Progression Free Survival)
Time from enrollment to first disease progression assessed by investigator or death due to any cause
Time frame: From start of treatment to 24 months
OS(Overall Survival)
Time from enrollment to the death of the subject due to any cause
Time frame: From start of treatment to 24 months
AE(Adverse Event)
incidece of adverse drug event
Time frame: From start of treatment to 24 months
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AUC=5,IV,Q3W