To investigate the feasibility, safety and tolerability of Preoperative Chemoradiation in Patients With Localized Gastric Cancer. Primary endpoint: R0 resection rate. Secondary endpoint: resection rate, pathological complete regression (pCR), effectiveness and safety of regime, disease free survival(DFS) and overall survival(OS).
The prognosis of gastric cancer is poor partially due to low R0 resection rate. Neoadjuvant chemoradiotherapy was reported to be effective in this setting by several phase II studies. The investigators aim to evaluate the efficacy and toxicity of neoadjuvant chemoradiotherapy in a prospective phase II study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
40
Radiation: 180 (cGy) /day, D1-5;S1: 50mg/m2,D1-5;
Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, China
RECRUITINGR0 resection rate
6-8 weeks after Radiation therapy,we evaluate the lesion,if it is resectable,we will give surgical therapy,
Time frame: 6-8 Weeks
safety and tolerability of the treatment regimen
after neoadjuvant chemotherapy and chemoradiotherapy,we evaluate the side effects , and record the side effects
Time frame: up to 10 weeks
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