Overview

Study of Weekly DCF to Treat Advanced Gastric Cancer

Status:
Terminated
Trial end date:
2008-06-01
Target enrollment:
0
Participant gender:
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 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Fudan University
Treatments:
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.