The Effect of Traditional Chinese Treatment Combined Adjuvant Chemotherapy in IIIb and IIIc Gastric Cancer (CHANGE)
Gastric Cancer Stage IIIB, Gastric Cancer Stage IIIC
About this trial
This is an interventional prevention trial for Gastric Cancer Stage IIIB
Eligibility Criteria
Inclusion Criteria:
- Histologically proven gastric carcinoma with radical operation, TNM (primary tumor, regional nodes, metastasis) stage IIIb or IIIc (The Eighth Edition American Joint Committee on Cancer [AJCC] gastric cancer staging);
- Karnofsky performance status higher than 70;
- Adequate hepatic, renal, cardio and hematologic function;
- With patients' consent and comply to long term follow-up.
Exclusion Criteria:
- Gastrectomy beyond D2, or TNM stage beyond Ⅲb and Ⅲc;
- Histological type beyond gastric carcinoma;
- Conversion chemotherapy before surgery;
- Concurrent cancer;
- Women of gravid or lactating; patients with mental illness;
- Uncontrolled significant comorbid conditions.
Sites / Locations
- Longhua Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
TCM combines CapOX/SOX/S-1+D/FLOT
CapOX/SOX/S-1+D/FLOT
Traditional Chinese Medicine oral taken twice a day for at least 3 months combined with chemotherapy. The chemotherapy can choose intravenous oxaliplatin 130 mg/m(2) on day 1 plus oral capecitabine 1000 mg/m(2) twice daily on days 1-14, every 21 days; or intravenous oxaliplatin 100 mg/m(2) on day 1 plus oral S-1 40mg/m(2) twice daily on days 1-14, every 21 days; or intravenous docetaxel 40mg/m(2) on day 1 plus oral S-1 40mg/m(2) twice daily on days 1-14, every 21 days; or intravenous docetaxel 50mg/m(2) on day 1 plus intravenous oxaliplatin 85 mg/m(2) on day 1 plus 5-FU intravenously CIV24h on day 1, every 14 days; Each participant shoud take eight (8) cycles of chemotherapy.
The chemotherapy can choose intravenous oxaliplatin 130 mg/m(2) on day 1 plus oral capecitabine 1000 mg/m(2) twice daily on days 1-14, every 21 days; or intravenous oxaliplatin 100 mg/m(2) on day 1 plus oral S-1 40mg/m(2) twice daily on days 1-14, every 21 days; or intravenous docetaxel 40mg/m(2) on day 1 plus oral S-1 40mg/m(2) twice daily on days 1-14, every 21 days; or intravenous docetaxel 50mg/m(2) on day 1 plus intravenous oxaliplatin 85 mg/m(2) on day 1 plus 5-FU intravenously CIV24h on day 1, every 14 days; Each participant shoud take eight (8) cycles of chemotherapy.