The purpose of this study is to assess the safety and effectiveness of Sintilimab Combined With Docetaxel in Non-driver Gene Mutation NSCLC patients who failed with double platinum-based chemotherapy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Sintilimab 200mg i.v q3w , Docetaxel 75mg/m2 i.v q3w
Hunan Provincal Tumor Hospital
Changsha, Hunan, China
Yongchang Z MD
Changsha, Hunan, China
ORR
To measure the patients's overall response rate
Time frame: Approximately 1 years
PFS
Progression free survival
Time frame: Approximately 1 years
OS
Overall survival
Time frame: Approximately 1 years
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