Docetaxel in Non Small Cell Lung Cancer (NSCLC)
- Conditions
- Carcinoma, Non-Small-Cell Lung
- Registration Number
- NCT00263016
- Lead Sponsor
- Sanofi
- Brief Summary
Primary Objective:
* To compare the tumour response rate of combination chemotherapy irinotecan/cisplatin (IC) versus docetaxel/cisplatin (DC) in advanced NSCLC patients who responded to 3 courses of docetaxel/cisplatin.
Secondary Objectives :
* To compare the time to progression after chemotherapy treatment between the IC and DC arms of treatment.
* To compare the toxicity profile of the IC and DC arms of treatment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 50
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Histologically or cytologically proven non-small cell lung carcinoma at first diagnosis.
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Stage IIIB or IV disease.
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Tumour considered unresectable.
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Performance status Karnofsky index > 60% or WHO performance status < or = 1.
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Previous therapy
- Chemotherapy: None.
- Previous radiation therapy: prior irradiation for NSCLC is permitted, however, the measurable or evaluable non-measurable disease must be completely outside the radiation portal.
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Laboratory requirements:
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Hematology:
- Neutrophils ≥ 2.0 10^9/l,
- Platelets ≥ 100 10^9/l,
- Hemoglobin ≥ 10 g/dl.
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Hepatic function:Total bilirubin < 1 Upper Normal Limit (UNL), AST (SGOT) and ALT (SGPT) < 2.5 UNL,Alkaline phosphatase < 5 UNL ; except in presence of only bone metastasis and in absence of any liver disorders. Patients with AST and/or ALT > 1.5 x UNL associated with alkaline phosphatase > 2.5 x UNL are not eligible for the study.
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Renal function: Creatinine < 140 µmol/l (1.6 mg/dl) ; if limit values, the calculated creatinine clearance should be > 60 ml/min.
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Pregnant, or lactating patients; patients of childbearing potential must implement adequate contraceptive measures during study participation.
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Known clinical brain or leptomeningeal involvement.
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Pre-existing motor or sensory neurotoxicity of a severity > grade 1 by National Cancer Institute criteria.
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Other serious illness or medical condition:
- Congestive heart failure or unstable angina pectoris even if it is medically controlled. Previous history of myocardial infarction within 1 year from study entry, uncontrolled hypertension or high risk uncontrolled arrhythmias.
- History of significant neurologic or psychiatric disorders including psychotic disorders, dementia or seizures that would prohibit the understanding and giving of informed consent.
- Active uncontrolled infection.
- Peptic ulcer, unstable diabetes mellitus or other contraindication for the use of corticosteroids.
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Past or current history of neoplasm other than non-small cell lung cancer, except for curatively treated non-melanoma skin cancer, in situ carcinoma of the cervix.
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Concurrent treatment with prednisone (or equivalent) except as use for the prophylactic medication regimen, treatment of acute hypersensitivity reactions, treatment of nausea / vomiting or unless chronic treatment (initiated > 6 months prior to study entry) at low dose (< 20 mg methylprednisolone or equivalent).
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Definite contraindications for the use of corticosteroids.
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Concurrent treatment with other experimental drugs. Participation in another clinical trial with any investigational drug within 30 days prior to study entry.
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Concurrent treatment with any other anti-cancer therapy.
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Tumour response rate Survival at 1 year
- Secondary Outcome Measures
Name Time Method Time to progression
Trial Locations
- Locations (1)
Sanofi-aventis
🇭🇰Hong Kong, Hong Kong