The purpose of this study is to determine whether sequential application of low-dose short-term sunitinib and chemotherapy is effective in the treatment of non-small cell lung cancer after failure of conventional therapy. Safety of this regimen will also be evaluated.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
sunitinib, 12.5mg/day, for 7 days before each cycle of chemotherapy; chemotherapy, single agent including docetaxel, albumin-bound paclitaxel, vinorelbine, gemcitabine, pemetrexed, or paclitaxel, as determined by the investigator
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Beijing, China
RECRUITINGprogression-free survival
The primary objective of this study is to evaluate the median progression-free survival of this sequential regimen.
Time frame: up to 2 years
overall survival
To evaluate the median over-all survival of this regimen
Time frame: up to 2 years
disease control rate
To evaluate the disease-control rate of this regimen.
Time frame: up to 6 months
Safety
To evaluate the safety of this regimen including the rate and grade of adverse effects.
Time frame: up to 2 years
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