RATIONALE: Celecoxib may slow the growth of cancer by stopping blood flow to the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining chemotherapy with celecoxib may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of combining celecoxib and docetaxel in treating patients who have advanced non-small cell lung cancer that has been previously treated with platinum -based chemotherapy.

Condition	Treatment or Intervention	Phase
stage IIIA non-small cell lung cancer stage IV non-small cell lung cancer stage IIIB non-small cell lung cancer recurrent non-small cell lung cancer	Procedure: chemotherapy  Procedure: biological response modifier therapy  Drug: chemosensitization/potentiation  Procedure: growth factor antagonist therapy  Procedure: anti-cytokine therapy  Procedure: antiangiogenesis therapy  Procedure: enzyme inhibitor therapy  Drug: celecoxib  Drug: docetaxel	Phase II

Further Study Details: 

OBJECTIVES: I. Determine the efficacy and feasibility of celecoxib combined with docetaxel in patients with advanced non-small cell lung cancer previously treated with platinum-based chemotherapy. II. Determine the response rate of patients treated with this regimen. III. Determine the toxicity of this regimen in these patients.

PROTOCOL OUTLINE: This is a multicenter study. Patients receive oral celecoxib twice daily (beginning on day -7 of the first course) and docetaxel IV over 1 hour on day 1. Treatment repeats every 21 days in the absence of disease progression or unacceptable toxicity. Patients who achieve a complete response (CR) receive 2 additional courses after CR. Patients who achieve stable disease (SD) or a partial response (PR) receive a minimum of 2 additional courses after SD or PR. At the discretion of the treating physician, patients then receive maintenance therapy comprising celecoxib only. Patients who discontinue therapy for disease progression or unacceptable toxicity are followed for at least 6 months.

PROJECTED ACCRUAL: A total of 21-39 patients will be accrued for this study within 13-28 months.

Ages Eligible for Study:  18 Years and above

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics--

• Diagnosis of stage IIIA, IIIB, or IV non-small cell lung cancer; Disease progression during or after 1 or more platinum-based chemotherapy regimens
• Measurable or evaluable disease
• No symptomatic or untreated brain or leptomeningeal metastases; Previously treated patients must be neurologically stable for 4 weeks after completion of appropriate therapy

--Prior/Concurrent Therapy--

• Biologic therapy: Not specified
• Chemotherapy: See Disease Characteristics; At least 4 weeks since prior chemotherapy; Prior paclitaxel allowed; No prior docetaxel
• Endocrine therapy: At least 3 days since prior steroids
• Radiotherapy: At least 4 weeks since prior radiotherapy; No prior radiotherapy to target lesion
• Surgery: At least 4 weeks since prior major surgery
• Other: Prior intermittent use of non-steroidal anti-inflammatory drugs (NSAIDs), including rofecoxib or celecoxib, allowed; At least 1 week since prior fluconazole; No recent prior NSAIDs, including rofecoxib or celecoxib, for a duration of more than 30 consecutive days; No concurrent fluconazole or lithium; No other concurrent NSAIDs except aspirin administered at a dose of no more than 325 mg/day for cardiovascular conditions; No other concurrent cyclo-oxygenase-2 inhibitors; No other concurrent investigational agents

--Patient Characteristics--

• Age: 18 and over
• Performance status: SWOG 0-2
• Life expectancy: Not specified
• Hematopoietic: Absolute neutrophil count at least 1,500/mm3; Platelet count at least 100,000/mm3; Hemoglobin at least 8 g/dL
• Hepatic: Bilirubin no greater than upper limit of normal (ULN); AST/ALT no greater than ULN (or no greater than 2.5 times ULN if alkaline phosphatase no greater than ULN); Alkaline phosphatase no greater than ULN (or no greater than 5 times ULN if AST/ALT no greater than ULN); No history of chronic hepatitis of any duration
• Renal: Creatinine no greater than ULN
• Cardiovascular: No uncontrolled congestive heart failure; No uncontrolled angina; No myocardial infarction and/or stroke within the past 6 months; No active thromboembolic event within the past 4 weeks
• Gastrointestinal: No gastrointestinal bleeding within the past 6 months; No history of peptic ulcer disease
• Other: No prior hypersensitivity reaction to docetaxel or other drugs formulated with polysorbate 80; No prior allergy to any non-steroidal anti-inflammatory drug; No other prior or concurrent malignancy within the past 3 years except adequately treated squamous cell or basal cell skin cancer or carcinoma in situ of the cervix; No grade 2 or greater peripheral neuropathy; No active infection; No other serious concurrent medical illness; No history of dementia, active psychiatric disorder, or other condition that would interfere with ability to take oral medication or preclude compliance with study; HIV negative; Must weigh at least 50 kg (110 pounds); Not pregnant or nursing; Negative pregnancy test; Fertile patients must use effective barrier contraception

Michigan
      Barbara Ann Karmanos Cancer Institute, Detroit,  Michigan,  48201-1379,  United States
      University of Michigan Comprehensive Cancer Center, Ann Arbor,  Michigan,  48109-0752,  United States

Study chairs or principal investigators

Shirish Gadgeel,  Study Chair,  Barbara Ann Karmanos Cancer Institute   

Study ID Numbers:  CDR0000069164; WSU-C-2304; NCI-V01-1688; AVENTIS-WSU-C-2304; WSU-06-08-01-M01-FB
Record last reviewed:  October 2003
Last Updated:  October 13, 2004
Record first received:  February 14, 2002
ClinicalTrials.gov Identifier:  NCT00030420
Health Authority: Unspecified
ClinicalTrials.gov processed this record on 2005-04-08