The purpose of this study is to assess the efficacy and safety of apatinib plus concurrent neoadjuvant chemoradiotherapy in patients with esophageal squamous cell carcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Apatinib Mesylate Tablets 250mg qd p.o. d1-35; Paclitaxel:50mg/m2 iv d1,8,15,22,29; Cisplatin: 30mg/m2 iv d1,8,15,22,29; RT:41.4Gy/23f , 1.8Gy/f,5 f/w
The pathological complete response rate(pCR)
The lesion disappeared completely by pathology
Time frame: within 3 weeks after surgery
R0-resection rate
There was no residual by the microscope
Time frame: within 3 weeks after surgery
Disease-free survival(DFS)
Baseline to measured date of recurrence or death from any cause
Time frame: 3 years
Overall survival (OS)
Baseline to measured date of death from any cause
Time frame: 1year
Adverse events Toxicity
Adverse events Toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0.The number of Participants with adverse events will be recorded at each treatment visit.
Time frame: 3 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.