RATIONALE: Drugs used in chemotherapy, such as docetaxel, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Thalidomide may stop the growth of non-small cell lung cancer by blocking blood flow to the tumor. Thalidomide may also help docetaxel work better by making tumor cells more sensitive to the drug. Giving docetaxel together with thalidomide may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving docetaxel together with thalidomide works as second-line therapy in treating patients with stage III or stage IV non-small cell lung cancer.
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DISEASE CHARACTERISTICS:
* Histologically or cytologically confirmed non-small cell lung cancer, meeting 1 of the following stage criteria:
* Stage IIIB (with pleural effusion)
* Stage IIIA or IIIB
* Previously treated and not eligible for surgery or definitive thoracic radiotherapy
* Stage IV
* Measurable or evaluable disease
* Documented disease progression during or after standard first-line chemotherapy that may have included taxane
* No untreated brain metastases
* Patients with previously treated brain metastases are eligible provided they have recovered from prior treatment
PATIENT CHARACTERISTICS:
Age
* 18 and over
Performance status
* ECOG 0-2
Life expectancy
* Not specified
Hematopoietic
* Absolute neutrophil count \> 1,500/mm\^3
* Hemoglobin ≥ 8.0 g/dL
* Platelet count \> 100,000/mm\^3
Hepatic
* Bilirubin normal
* SGOT and/or SGPT ≤ 2.5 times upper limit of normal (ULN) AND alkaline phosphatase normal OR
* SGOT and/or SGPT normal AND alkaline phosphatase ≤ 4 times ULN AND no ascites
* Albumin \> 3.0 g/dL
Renal
* Creatinine \< 1.5 mg/dL
Other
* Not pregnant or nursing
* Negative pregnancy test
* Fertile patients must use effective double-method contraception for 4 weeks before, during, and for ≥ 4 weeks after completion of study treatment
* No HIV positivity
* No peripheral neuropathy \> grade 1
* No other malignancy within the past 5 years except inactive nonmelanoma skin cancer or carcinoma in situ of the cervix or breast
* No active infections
* No history of severe hypersensitivity reaction to docetaxel or other drugs formulated with polysorbate 80
PRIOR CONCURRENT THERAPY:
Biologic therapy
* Not specified
Chemotherapy
* See Disease Characteristics
* No more than 1 prior systemic chemotherapy regimen for locally advanced or metastatic disease
* Prior neoadjuvant or adjuvant systemic chemotherapy allowed
* At least 4 weeks since prior chemotherapy and recovered
Endocrine therapy
* Not specified
Radiotherapy
* Recovered from prior radiotherapy
Surgery
* Not specified
Other
* No other concurrent investigational agents
* No other concurrent anticancer therapy