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

Inclusion Criteria

• •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:
• •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
• •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