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. PI-88 may stop the growth of non-small cell lung cancer by blocking blood flow to the tumor. It may also help docetaxel work better by making tumor cells more sensitive to the drug. Giving docetaxel together with PI-88 may kill more tumor cells. It is not yet known whether giving docetaxel together with PI-88 is more effective than docetaxel alone in treating non-small cell lung cancer.

PURPOSE: This randomized phase II trial is studying docetaxel and PI-88 to see how well they work when given together compared to docetaxel alone in treating patients with stage IIIB or stage IV non-small cell lung cancer.

Condition	Treatment or Intervention	Phase
recurrent non-small cell lung cancer stage IIIB non-small cell lung cancer stage IV non-small cell lung cancer	Drug: PI-88  Drug: docetaxel  Procedure: anti-cytokine therapy  Procedure: antiangiogenesis therapy  Procedure: biological response modifier therapy  Procedure: chemosensitization/potentiation  Procedure: chemotherapy  Procedure: growth factor antagonist therapy	Phase II

Further Study Details: 

OBJECTIVES: Primary

• Compare the safety and efficacy of docetaxel with vs without PI-88 in patients with stage IIIB or IV non-small cell lung cancer.

Secondary

• Determine the efficacy markers of docetaxel and PI-88 in these patients.
• Determine the safety and potential efficacy of PI-88 alone as maintenance therapy in patients whose disease has been controlled with docetaxel and PI-88 combination therapy.
• Determine the safety and potential efficacy of PI-88 alone as third-line therapy in these patients.

OUTLINE: This is an open-label, randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients receive docetaxel IV over 1 hour on days 1, 8, and 15.
• Arm II: Patients receive docetaxel as in arm I. Patients also receive PI-88 subcutaneously once daily on days 1-4, 8-11, and 15-18. In both arms, treatment repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. Patients in arm II with stable or responding disease after 6 courses may continue to receive PI-88 alone as maintenance therapy. Patients in arm I with progressive disease or unacceptable toxicity before the completion of 6 courses may receive PI-88 alone as third-line therapy.

PROJECTED ACCRUAL: Approximately 100 patients will be accrued for this study.

Ages Eligible for Study:  18 Years and above,  Genders Eligible for Study:  Both

Criteria

DISEASE CHARACTERISTICS:

• Diagnosis of non-small cell lung cancer
• Stage IIIB or IV disease
• Eligible for second-line docetaxel
• Disease progression during or after completion of prior first-line therapy comprising radiotherapy and/or platinum-based chemotherapy

PATIENT CHARACTERISTICS: Age

• 18 and over

Performance status

• ECOG 0-1

Life expectancy

• At least 2 months

Hematopoietic

• Neutrophil count > 1,500/mm^3
• Platelet count > 100,000/mm^3
• WBC > 3,000/mm^3
• No history of thrombotic thrombocytopenic purpura or other platelet disease

Hepatic

• Bilirubin normal
• ALT and AST ≤ 2.5 times upper limit of normal (ULN) (1.5 times ULN if alkaline phosphatase > 2.5 times ULN)
• Alkaline phosphatase ≤ 5 times ULN (unless bone metastases are present)
• PT < 1.5 times ULN
• Activated PTT normal

Renal

• Creatinine clearance or glomerular filtration rate > 50mL/min

Cardiovascular

• None of the following within the past 3 months:
• Myocardial infarction
• Stroke
• Congestive heart failure

Immunologic

• No history of immune-mediated thrombocytopenia
• No evidence of anti-heparin antibodies
• No history of allergy and/or hypersensitivity to anti-coagulants or thrombolytic agents, especially heparin
• No history of allergy to polysorbate 80
• No uncontrolled or serious infection within the past 4 weeks

Other

• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy

• Not specified

Chemotherapy

• See Disease Characteristics
• No prior docetaxel

Endocrine therapy

• Not specified

Radiotherapy

• See Disease Characteristics
• More than 3 months since prior radiotherapy to > 30% of marrow-bearing bone
• Concurrent local palliative radiotherapy allowed

Surgery

• More than 4 weeks since prior major surgery

Other

• More than 4 weeks since prior antineoplastic therapy
• More than 2 weeks since prior and no concurrent heparin or low-molecular weight heparin
• More than 4 weeks since prior investigational therapy
• No concurrent aspirin or aspirin-containing medications except low-dose aspirin (≤ 100 mg/day)
• No concurrent nonsteroidal anti-inflammatory drugs except cyclooxygenase-2 inhibitors
• No concurrent warfarin or warfarin-containing medications except low-dose warfarin (≤ 1 mg/day)
• No concurrent antiplatelet drugs, including any of the following:
• Abciximab
• Clopidogrel
• Dipyridamole
• Ticlopidine
• Tirofiban
• No concurrent drugs that may inhibit docetaxel metabolism, including any of the following:
• Cyclosporine
• Terfenadine
• Ketoconazole
• Erythromycin
• Troleandomycin
• No other concurrent investigational drugs
• No other concurrent antineoplastic therapy

Australia, Australian Capital Territory
      Canberra Hospital, Garran,  Australian Capital Territory,  2605,  Australia; Recruiting
Australia, New South Wales
      Concord Repatriation General Hospital, Concord,  New South Wales,  2139,  Australia; Recruiting
      Institute of Oncology at Prince of Wales Hospital, Randwick,  New South Wales,  2031,  Australia; Recruiting
      Newcastle Mater Misericordiae Hospital, Waratah,  New South Wales,  2298,  Australia; Recruiting
      Royal North Shore Hospital, St. Leonards,  New South Wales,  2065,  Australia; Recruiting
      Sydney Cancer Centre at Royal Prince Alfred Hospital, Sydney,  New South Wales,  2050,  Australia; Recruiting
      Sydney Heamatology and Oncology Clinics, Hornsby,  New South Wales,  2077,  Australia; Recruiting
Australia, Queensland
      Mater Medical Centre, South Brisbane,  Queensland,  4101,  Australia; Recruiting
      Nambour General Hospital, Nambour,  Queensland,  4560,  Australia; Recruiting
      Prince Charles Hospital, Chermside,  Queensland,  4032,  Australia; Recruiting
      Princess Alexandra Hospital, Brisbane,  Queensland,  4102,  Australia; Recruiting
Australia, South Australia
      Queen Elizabeth Hospital, Woodville,  South Australia,  5011,  Australia; Recruiting
Australia, Victoria
      Alfred Hospital, Melbourne,  Victoria,  3004,  Australia; Recruiting
      Murray Valley Private Hospital, Wodonga,  Victoria,  3690,  Australia; Recruiting
Australia, Western Australia
      Sir Charles Gairdner Hospital - Perth, Perth,  Western Australia,  6009,  Australia; Recruiting

Study chairs or principal investigators

Nick Pavlakis, MD,  Study Chair,  Royal North Shore Hospital   

Study ID Numbers:  CDR0000409568; PROGEN-PR88202; AUS-RNSH-0309-183M; NCT00103389
Record last reviewed:  January 2005
Last Updated:  April 4, 2005
Record first received:  February 7, 2005
ClinicalTrials.gov Identifier:  NCT00103389
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08