Bexarotene, Tretinoin, and Combination Chemotherapy in Treating Patients With Stage III or Stage IV Non-Small Cell Lung Cancer

DISEASE CHARACTERISTICS:

Histologically or cytologically confirmed non-small cell lung cancer (NSCLC)

Stage IIIB disease with a malignant pleural effusion
Stage IV disease
Chemotherapy-naive disease
Brain metastases allowed provided patients have completed radiation treatment with no actively progressing brain metastases

PATIENT CHARACTERISTICS:

Inclusion criteria:

ECOG performance status 0-2

Absence of hepatic dysfunction that is characterized by the following:

AST/ALT > 3 times upper limit of normal (ULN) (unless due to liver metastases)
Bilirubin > 3 times ULN (unless due to liver metastases)
ANC ≥ 1,500/mm^3
Platelets ≥ 100,000/mm^3
Negative pregnancy test prior to the initiation of treatment
Female and male patients of childbearing potential must agree to sexual abstinence for at least 4 weeks prior to study OR practice 2 reliable forms of effective contraception simultaneously (strongly recommended that one of the two forms of contraception be non-hormonal) at least 4 weeks prior to, during the entire study treatment, and for at least 1 month after treatment is discontinued
Male patients with female sexual partners who are pregnant, possibly pregnant, or who could become pregnant during the study must agree to use condoms during sexual intercourse during the entire study treatment and for at least 1 month after the last dose of bexarotene
Must be willing and able to give informed consent, comply with study instructions, and commit to all study visits

Exclusion criteria:

Pregnancy, intent to become pregnant, or breast-feeding
Significant concurrent or intercurrent illness
Risk factor for pancreatitis (e.g., uncontrolled hyperlipidemia, excessive alcohol consumption, uncontrolled diabetes mellitus, biliary tract disease)
Untreated hypothyroidism
Active second malignancy with the exception of carcinoma in situ, early-stage prostate cancer, and squamous or basal cell carcinoma of skin
Unwillingness or inability to minimize exposure to sunlight and artificial ultraviolet light while receiving bexarotene
Known contraindication (according to product labeling) to Lipitor^® (or another selected lipid lowering agent) or levothyroxine
Known hypersensitivity to bexarotene or other component of bexarotene

PRIOR CONCURRENT THERAPY:

Inclusion criteria

Tyrosine kinase inhibitor therapy such as erlotinib hydrochloride is allowed for up to 3 months prior to initiation of this regimen provided the disease is unresponsive to such treatment
Concurrent radiation therapy administered for symptom relief
Also see Disease Characteristics

Exclusion criteria

Prior therapy, except radiation to the brain for palliation, as long as a measurable lesion is still present
Prior use of bexarotene
Prior systemic anticancer therapy (e.g., immunotherapy, chemotherapy, or biologic modifier therapy)
Medication known to increase triglyceride levels or associated with pancreatic toxicity
Systemic vitamin A in doses exceeding 15,000 IU/day within 14 days prior to initiating study therapy
Concurrent gemfibrozil (Lopid^®)
Concurrent anticancer therapy of any kind other than that mandated by the protocol