Overview
Study of Weekly DCF to Treat Advanced Gastric Cancer
Status:
Terminated
Terminated
Trial end date:
2008-06-01
2008-06-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to evaluate the efficacy of weekly docetaxol combined with cisplatin and 5-Fu in patients with AGC.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Fudan UniversityTreatments:
Cisplatin
Docetaxel
Criteria
Inclusion Criteria:- Age between 18 and 70 years
- Patients with histologically confirmed, unresectable, recurrent and/or metastatic
gastric adenocarcinoma
- ECOG performance status ≤1,life expectancy more than 3 months,
- Normal laboratory findings:absolute neutrophil count and platelet count ≥ 2.0×109/L
and 80×109/L, respectively, hepatic function (total serum bilirubin ≤ UNL,
transaminases ≤ 1.5 times upper normal limit) and renal function (calculated
creatinine clearance ≥ 60 ml/min).
- Measurable disease according to the RECIST.
Exclusion Criteria:
- Pregnant or lactating women
- Serious uncontrolled diseases and intercurrent infection
- The evidence of CNS metastasis
- History of other malignancies except cured basal cell carcinoma of skin and carcinoma
in-situ of uterine cervix
- Received other chemotherapy regimen after metastasis
- Used taxane in adjuvant settings
- Participated in other clinical trials.