This trial is active, not recruiting.

Condition lung cancer
Treatments pi-88, docetaxel
Phase phase 2
Sponsor Progen Pharmaceuticals
Start date February 2004
Trial identifier NCT00103389, AUS-RNSH-0309-183M, CDR0000409568, PROGEN-PR88202


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.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Masking open label
Primary purpose treatment

Primary Outcomes

Proportion of patients who are progression-free as measured by Response Evaluation Criteria in Solid Tumors (RECIST) v2.0 at 6 months
time frame:
Non-progression rate as measured by RECIST v2.0 at 6 months
time frame:

Secondary Outcomes

Time to progression as measured by RECIST v2.0 at baseline, and then week 4 of courses 2, 3, 4, and 6
time frame:
Response rate as measured by RECIST v2.0 at baseline, and then week 4 of courses 2, 3, 4, and 6
time frame:
Quality of life as measured by Lung Cancer Symptom Scale (LCSS) every month
time frame:
Overall survival as measured by RECIST v2.0 at death
time frame:

Eligibility Criteria

Male or female participants at least 18 years old.

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

Additional Information

Official title A Phase II Study of Docetaxel With PI-88 in Patients With Advanced Non-Small-Cell Lung Cancer
Description 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.
Trial information was received from ClinicalTrials.gov and was last updated in September 2008.
Information provided to ClinicalTrials.gov by National Cancer Institute (NCI).