Expired Study
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Philadelphia, Pennsylvania 19104


Purpose:

This clinical trial is studying the amount of EF5 and motexafin lutetium present in tumor cells and/or normal tissues of patients with abdominal (such as ovarian, colon, or stomach cancer) or non-small cell lung cancer. EF5 may be effective in measuring oxygen in tumor tissue. Photosensitizing drugs such as motexafin lutetium are absorbed by tumor cells and, when exposed to light, become active and kill the tumor cells. Knowing the level of oxygen in tumor tissue and the level of motexafin lutetium absorbed by tumors and normal tissue may help predict the effectiveness of anticancer therapy


Study summary:

OBJECTIVES: I. Determine the uptake of motexafin lutetium in tumors and normal tissue of patients with intra-abdominal malignancies or non-small cell lung cancer. II. Determine the ratio of tumor to normal tissue by measuring the level of motexafin lutetium uptake in tumor and normal tissue removed from these patients. III. Determine the pattern, presence, and level of EF5 binding (as a surrogate marker for hypoxia) in tumors of these patients. IV. Determine the feasibility of measuring optical properties, tissue oxygenation, motexafin lutetium concentration, fluorescence, and blood flow by non-invasive means in these patients. OUTLINE: This is a multicenter, diagnostic study. Patients are stratified according to diagnosis (intra-abdominal malignancy vs non-small cell lung cancer). Patients receive EF5 IV over 1-2.5 hours on day 1 and motexafin lutetium IV over 10-15 minutes on day 2. Patients undergo definitive surgical resection approximately 3 hours after motexafin lutetium administration. Hypoxia and motexafin lutetium levels in the resected tumors are evaluated. Tumor to normal tissue ratios are also determined. After completion of study treatment, patients are followed at approximately 1-8 weeks. PROJECTED ACCRUAL: A total of 30 patients (20 with intra-abdominal malignancies and 10 with non-small cell lung cancer) will be accrued for this study within 10-15 months.


Criteria:

Inclusion Criteria: - Histologically confirmed or suspected diagnosis of 1 of the following: - Intra-abdominal malignancy of 1 of the following types: - Sarcoma - Ovarian cancer - Gastrointestinal malignancies, including, but not limited to, appendiceal cancer, colon cancer, or gastric cancer - Non-small cell lung cancer - Planning to undergo surgical resection of disease - Disease has the propensity to spread to the peritoneal cavity (intra-abdominal malignancy patients) - Performance status - ECOG 0-2 - WBC ≥ 2,000/mm^3 - Platelet count ≥ 100,000/mm^3 - Bilirubin < 1.5 mg/dL - Creatinine normal - Creatinine clearance ≥ 60 mL/min - Body weight ≤ 130 kg - No G6PD deficiency - No porphyria - No history of peripheral neuropathy ≥ grade 3 - Able to tolerate anesthesia and major surgery - Not pregnant or nursing - Negative pregnancy test - Fertile patients must use effective contraception during and for 1 month after study participation


NCT ID:

NCT00087191


Primary Contact:

Principal Investigator
Stephen Michael Hahn
Abramson Cancer Center of the University of Pennsylvania


Backup Contact:

N/A


Location Contact:

Philadelphia, Pennsylvania 19104
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 10, 2017

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