The purpose of this study is to evaluate the efficacy of apatinib mesylate combined with pemetrexed alone in advanced non-small cell lung cancer patients in the second or second line of treatment of progression-free survival
It is a one-arm study. The progression-free survival will be evaluated.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
48
For those pretreated non-squamous non-small cell lung cancer, treat with apatinib 500mg Qd, po.combined with pemetrexed continue until disease progression
Ou wuling
Wuhan, Hubei, China
RECRUITINGprogression free survival
evaluation per 28 days
Time frame: 4 weeks
Overall Survival
evaluation per 28 days
Time frame: 4 weeks
disease control rate
evaluation per 28 days
Time frame: 4 weeks
objective response rate
evaluation per 28 days
Time frame: 4 weeks
Adverse Event
evaluation per 28 days
Time frame: 4 weeks
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