This is a non-randomized, phase II, open label study of radiotherapy concurrent with Apatinib Mesylate after surgery in patients with advanced head and neck soft tissue and bone sarcomas. The primary purpose of this study is to evaluate the efficacy and safety of Apatinib Mesylate in patients with head and neck soft tissue and bone sarcomas.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
61
Apatinib Mesylate will be administered orally at 500 mg once daily from 2 weeks before the beginning of radiotherapy until the end of whole radiotherapy course
Shanghai ninth people's hospital
Shanghai, Shanghai Municipality, China
Progression-free survival(PFS)
To determine 2 year PFS of Apatinib Mesylate when administered as monotherapy in patients with metastatic adenoid cystic carcinoma
Time frame: 2 year
Overall survival rate
from date of enrollment until date of first death from any cause, assessed up to 2 years
Time frame: 2 year
Number of participants with treatment-related adverse events as assessed by CTCAE v3.0
Time frame: through study completion, an average of 2 years
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