Stomach Neoplasms
Conditions
Brief summary
Study objectives: To determine Ro resection rate of Docetaxel, cisplatin and fluorouracil combination for the treatment of neoadjuvant gastric carcinoma.
Interventions
DRUGDocetaxel
Formulation: infusion solution Route of administration: IV infusion on the first day of each 21-day cycle Dose regimen: 75 mg/m2
DRUGCisplatin
Formulation: infusion solution Route of administration: IV infusion on the first day of each 21-day cycle Dose regimen: 75 mg/m2
DRUGFluorouracil
Formulation: infusion solution Route of administration: IV infusion on the first day of each 21-day cycle Dose regimen: 750 mg/m2/day for 5 days
Sponsors
Sanofi
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
* Histologically proven gastric adenocarcinoma diagnosis * Selected Stage IIB (T3N0M0), Stage IIIA (T2aN2M0, T2bN2M0, T3N1M0, T4N0M0), Stage IIIB (T3N2M0) and selected Stage IV (all T4 , NM0, all TN3M0's). Clinical staging performed with endoscopic ultrasound and CT. Laparotomy or laparoscopy is preferred to determine resectability and peritoneal involvement. * ECOG performance status between 0 and 2 * Acceptable hematological profile : * WBC (White Blood Cell) count ≥4000/mm3 * Platelet count ≥100 000 mm3 * Hemoglobin ≥9 g/100 mL (if lower, may be included following transfusion) * Adequate renal function * Serum creatinine \<1.2 mg/dl or calculated creatinine clearance in 24-hours urine \>60 mL/min. * Adequate hepatic function * Bilirubin \< UNL * Transaminases (ALT, AST) \<2.5 x UNL * Alcaline phosphatase \<2.5 x UNL * Adequate pulmonary function * Adequate cardiac function * No prior chemotherapy for gastric cancer
Exclusion criteria
* Other histological types of gastric cancer (leiomyosarcoma, lymphoma) than adenocarcinoma * Pregnant or lactating patients * Patients with brain, bone or other metastases; peritoneal involvement * Other serious underlying medical conditions which could impair the ability of the patient to participate in the study (congestive heart failure, serious arrhythmia, uncontrolled diabetes mellitus, serious neuropathy), history of myocardial infarction within 6 months prior to study entry * Previous or other current malignancies, with the exception of carcinoma of the cervix uteri or breast cancer or basal cell skin cancer and a disease-free period shorter than 5 years * Active infection and other serious disease * Any other experimental drugs within a 4-week period prior to the study * Contraindications for the use of any study drug (e.g. history of hypersensitivity to the contents of the study drugs) The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the R0 resection rate for the treatment of locally advanced gastric carcinoma with Docetaxel, Cisplatin, Fluorouracil combination. | 3 cycles |
Countries
Turkey (Türkiye)
Outcome results
None listed