Phase II Study of Oxaliplatin / Irinotecan / Bevacizumab Followed by Docetaxel / Bevacizumab in Inoperable Locally Advanced or Metastatic Gastric Cancer Patients
- Conditions
- nresectable locally advanced or metastatic Gastric CancerMedDRA version: 20.0Level: PTClassification code 10063916Term: Metastatic gastric cancerSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)Therapeutic area: Diseases [C] - Cancer [C04]
- Registration Number
- EUCTR2008-006128-79-AT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 40
•Signed informed consent
•Histologically proven gastric adenocarcinoma
•Measurable or evaluable, inoperable locally advanced or metastatic disease
•No previous palliative chemotherapy and/or immunotherapy
•Life expectancy of more than 3 months
•Age = 18 years.
•ECOG performance status 0 – 2
•Ability to understand and comply with requirements of study protocol and trial participation
•Patients of either sex are eligible for study entry. Women of childbearing potential must have a negative pregnancy test at screening and must use effective contraception (e.g. intrauterine device (IUD), birth control pills, or barrier device) beginning 2 weeks prior to first dose of study drug until 6 months after the final dose of study drug.
•Hematological status:
Leucocytes = 3 x 109/l
Platelets = 100 x 109/l
•Renal function:
Serum creatinine: = 1.5 x upper normal limit of normal (ULN)
•Hepatic function:
AST and ALT: < 2.5 x ULN or < 5 x ULN if hepatic metastases are present
Alkaline phosphatase: < 2.5 x ULN or < 5 x ULN if hepatic metastases are present
Total bilirubin level = 1.5 x ULN
•Patient must have an INR = 1.5 and aPTT = 1.5 x ULN within 7 days prior to randomisation
•Baseline evaluations performed before treatment start: clinical and blood evaluations no more than 7 days prior to planned first course; tumoral assessment (CT scan or MRI) no more than 4 weeks prior to planned first course
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 40
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 40
•Pregnant or lactating women.
•Women of child-bearing potential and men not using effective contraception.
•Concurrent cancer therapy (chemotherapy, radiation therapy, immunotherapy, biologic therapy) or
•Neo/Adjuvant treatment with Bevacizumab
•Patients with locally advanced disease who are candidates for curative therapy (including operation and/or chemotherapy and/or radiotherapy).
•Prior history of chronic enteropathy, chronic diarrhea, unresolved bowel obstruction/ subobstruction, or extensive abdominopelvic radiation therapy.
•Previous malignancy other than gastric cancer in the last 5 years except curatively treated basal cell carcinoma of the skin and/or in situ carcinoma of the cervix.
•Evidence of CNS metastasis at baseline. A CT or MRI scan within 28 days prior to randomisation is mandatory to exclude CNS involvement in case of clinical suspicion of CNS metastasis.
•Peripheral neuropathy (NCI CTC grade = 1).
•Inadequate renal function:
•adequate renal function:ould be = 60 mL/min. The Cockroft and Gault formula is recommended for calculation of creatinine clearance. Patients with a creatinine clearance just below 60 ml/min may be eligible if a measured creatinine clearance (based on 24 hour urine collection or other reliable method) is = 60 mL/min.
• Urine dipstick for proteinuria should be < 2+. Patients with = 2+ proteinuria on dipstick urinalysis at baseline should undergo 24 hour urine collection and must demonstrate < 1 g of protein/24 hr.
•Serious medical or psychiatric disorders that would interfere with the patient’s informed consent or compliance with the requirements of the protocol or that contraindicates the use of an investigational drug or puts the patient at high risk for treatment-related complications.
•Active bacterial, viral or fungal infection (including acute or chronic-active infection with HBV or HCV).
•Acute intra abdominal inflammatory process.
•Uncontrolled hypertension (systolic > 150 mm Hg and/or diastolic > 100 mm Hg) or clinically significant (i.e. active) cardiovascular disease, for example cerebrovascular accidents (= 6 months prior to randomisation), myocardial infarction (= 6 months prior to randomisation), unstable angina, New York Heart Association Grade II or greater congestive heart failure, or serious cardiac arrhythmia uncontrolled by medication or potentially interfering with protocol treatment.
•Prior history of hypertensive crisis or hypertensive encephalopathy.
•Evidence of tumour invading major blood vessels on imaging. The investigator or the local radiologist must exclude evidence of tumour that is fully contiguous with, surrounding, or extending into the lumen of a major blood vessel (e.g. pulmonary artery or superior vena cava).
•Serious uncontrolled coagulation disorder or thrombo-embolic complications (history of embolisms or thromboses) within 6 months prior to study start or history of inherited bleeding diathesis or coagulopathy with the risk of bleeding.
•Major surgical procedures within 4 weeks prior to study entry or planned major surgical procedures throughout the course of the study. Patients must have fully recovered from any surgical procedures conducted prior to 4 weeks before study entry.
•Minor surgery, including insertion of an indwelling catheter, within 48 hours prior to the first bevacizumab infusion.
•Concurrent or recent (within 10 days) anticoagulant therapy. Prophylactic use of anticoagulants is allowed.
•Chronic daily treatment with aspirin (> 325 mg/da
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method