Overview

Carboplatin and Paclitaxel in Treating Older Patients With Metastatic or Recurrent Unresectable Non-small Cell Lung Cancer

Status:
Completed
Trial end date:
2006-04-01
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: Phase II trial to study the effectiveness of carboplatin and paclitaxel in treating patients who have metastatic or recurrent unresectable 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:
Albumin-Bound Paclitaxel
Carboplatin
Paclitaxel
Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed non-small cell lung
cancer Stage IV disease OR Recurrent unresectable disease No other conventional curative or
significant palliative therapies available Measurable disease At least one lesion a minimum
of one dimension in diameter of at least 20 mm No symptomatic and/or untreated CNS
metastases

PATIENT CHARACTERISTICS: Age: 65 and over Performance status: ECOG 0-2 Life expectancy: At
least 12 weeks Hematopoietic: Absolute neutrophil count at least 1,500/mm3 Platelet count
at least 100,000/mm3 Hepatic: AST no greater than 3 times upper limit of normal Renal:
Creatinine clearance at least 40 mL/min Other: No uncontrolled infection No uncontrolled
seizure disorder No uncontrolled diabetes mellitus No other malignancies within the past 3
years except adequately treated basal or squamous cell skin cancer or noninvasive
carcinomas

PRIOR CONCURRENT THERAPY: Biologic therapy: No prior biologic or immunotherapy for
recurrent or metastatic disease No concurrent biologic therapy Chemotherapy: No prior
chemotherapy for recurrent or metastatic disease except as radiosensitizer No other
concurrent chemotherapy Endocrine therapy: Not specified Radiotherapy: No prior
radiotherapy for recurrent or metastatic disease except as adjuvant therapy At least 4
weeks since prior radiotherapy to greater than 25% of bone marrow No concurrent
radiotherapy except for CNS therapy Surgery: See Disease Characteristics At least 3 weeks
since prior major surgery