Overview

Docetaxel and Gemcitabine in Treating Patients With Stage IIIB or Stage IV Non-small Cell Lung Cancer

Status:
Completed
Trial end date:
2008-05-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Randomized phase II trial to compare the effectiveness of two regimens of docetaxel plus gemcitabine in treating patients who have stage IIIB or stage IV non-small cell lung cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Alliance for Clinical Trials in Oncology
Collaborator:
National Cancer Institute (NCI)
Treatments:
Docetaxel
Gemcitabine
Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed stage IIIB/IV nonsmall
cell lung cancer eligible for first line chemotherapy Measurable disease (must be outside
radiation port or proof of progressive disease) Metastatic CNS disease allowed if treated
and stable for at least 21 days prior to study

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-1 Life expectancy:
Greater than 12 weeks Hematopoietic: Platelet count at least 100,000/mm3 Hemoglobin at
least 10 g/dL Absolute neutrophil count at least 1500/mm3 Hepatic: Bilirubin no greater
than upper limit of normal (ULN) Alkaline phosphatase no greater than 3 times ULN AST no
greater than 2.5 times ULN Renal: Creatinine no greater than 1.5 times ULN Cardiovascular:
At least 3 months since prior myocardial infarction No uncontrolled congestive heart
failure No uncontrolled arrhythmias Other: Not pregnant or nursing Fertile patients must
use effective contraception Peripheral neuropathy less than grade 2 No history of
hypersensitivity to products containing polysorbate 80 No other significant medical
condition No meningeal carcinomatosis No weight loss of greater than 10% within past 3
months due to disease

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: No prior
chemotherapy Endocrine therapy: Not specified Radiotherapy: At least 4 weeks since prior
radiotherapy to pelvis, spine, or long bones and recovered No prior radiotherapy to at
least 30% of bone marrow Surgery: Greater than 4 weeks since prior major surgery Other: At
least 3 weeks since prior investigational drugs