To evaluate the efficacy and safety of apatinib in treating patients with recurrent or metastatic nasopharyngeal carcinoma who failed prior platinum based chemotherapy
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
51
500 mg qd p.o. and it should be continued until disease progression or intolerable toxicity or patients withdrawal of consent
Xiaozhong Chen
Hangzhou, Zhejiang, China
RECRUITINGCBR(Clinical Benefit Rate)
The sum rate of complete response, partial response and stable disease
Time frame: 12 weeks
The incidence of Grade 3-4 adverse events
Number of participants with adverse events and serious adverse events.In addition,estimating their relationship with apatinib.
Time frame: 2 years
PFS (progression free survival)
from the first day of therapy to the date of disease progression or death from any cause, whichever was first (according the criterion of RECIST 1.1 ).
Time frame: 2 years
OS (overall survival)
from the first day of therapy to death or last follow-up
Time frame: 2 years
QoL(quality of life)
Changes in quality of life were assessed by EORTC QLQ-C30
Time frame: 2 years
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