RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as bevacizumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Combining chemotherapy and monoclonal antibodies may kill more tumor cells.

PURPOSE: Randomized phase II/III trial to study the effectiveness of combination chemotherapy with or without bevacizumab in treating patients who have advanced, metastatic, or recurrent non-small cell lung cancer.

OBJECTIVES:

• Compare the toxicity of paclitaxel and carboplatin with or without bevacizumab in patients with advanced, metastatic, or recurrent non-squamous cell non-small cell lung cancer.
• Compare the survival of patients treated with these regimens.
• Compare the response rates and time to progression in patients treated with these regimens.

OUTLINE: This is a randomized study. Patients are stratified according to measurable disease (yes vs no), prior radiotherapy (yes vs no), weight loss (less than 5% vs 5% or more), and disease stage (IIIB vs IV vs recurrent). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive paclitaxel IV over 3 hours followed by carboplatin IV over 15-30 minutes on day 1.
• Arm II: Patients receive paclitaxel and carboplatin as in arm I followed by bevacizumab IV over 30-90 minutes on day 1.

Treatment in both arms repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.

After completion of 6 courses, patients in arm II with stable or responding disease continue to receive bevacizumab only. Treatment repeats every 3 weeks in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months for 2 years and then every 6 months for 3 years.

PROJECTED ACCRUAL: A total of 842 patients will be accrued for this study.

DISEASE CHARACTERISTICS:

• Histologically or cytologically confirmed non-small cell lung cancer (NSCLC)
• Stage IIIB with malignant pleural effusion, stage IV, or recurrent
• Measurable or nonmeasurable disease
• No squamous cell NSCLC
• No known CNS metastases by head CT scan or MRI within the past 4 weeks

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• ECOG 0-1

Life expectancy:

• Not specified

Hematopoietic:

• Absolute neutrophil count at least 1,500/mm^3
• Platelet count at least 100,000/mm^3
• No prior thrombotic or hemorrhagic disorders

Hepatic:

• Bilirubin no greater than 1.5 mg/dL
• Transaminases no greater than 5 times upper limit of normal (ULN)
• PTT normal
• INR no greater than 1.5

Renal:

• Creatinine no greater than 1.5 times ULN
• Urine protein less than 1+ (i.e., trace or 0 by dipstick or urinalysis) OR
• 24-hour urine protein less than 500 mg

Cardiovascular:

• No symptomatic congestive heart failure
• No unstable angina pectoris
• No cardiac arrhythmia
• Concurrent hypertension allowed provided well-controlled on a stable regimen of anti-hypertensive therapy

Pulmonary:

• No history of gross hemoptysis (½ teaspoon of bright red blood or more)

Other:

• No ongoing or active infection
• No serious non-healing wound ulcer
• No bone fracture
• No psychiatric illness or social situation that would preclude study compliance
• No other concurrent comorbidities that would preclude study participation
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• At least 3 weeks since prior immunotherapy and recovered

Chemotherapy:

• No prior systemic chemotherapy

Endocrine therapy:

• At least 3 weeks since prior hormonal therapy and recovered

Radiotherapy:

• At least 3 weeks since prior radiotherapy and recovered

Surgery:

• At least 3 weeks since prior major surgery

Other:

• No concurrent therapeutic anticoagulation
• No concurrent chronic daily aspirin (greater than 325 mg/day)
• No concurrent non-steroidal anti-inflammatory agents known to inhibit platelet function (arm II only)
• No concurrent dipyridamole, ticlopidine, clopidogrel, and/or cilostazol