The primary purpose of this study is to assess the safety and feasibility of giving TNFerade™ with 5-FU, Cisplatin and radiation therapy to patients with locally advanced, esophageal cancer prior to surgical resection. TNFerade™ is a replication deficient (E1, E3 and E4 deleted) adenovirus vector containing the gene for TNF-alpha controlled by a radiation inducible promoter. This allows the expression of TNF-alpha to be greatest in the area receiving radiation. TNF-alpha is a potent cytokine that has been shown to have potent anti-cancer activities but, due to systemic toxicity, could not be delivered at effective doses. TNFerade™ is a novel way of selective delivery of TNF-alpha to tumor cells. TNFerade™ will be delivered once a week for five weeks by direct intratumoral injection by using endoscopy or Endoscopic Ultrasound. 5-FU (1000 mg/m2/day) will be delivered via continuous infusion for 96 hours during weeks 1 and 4. Cisplatin (75 mg/m2) will be delivered on Day 1 and Day 29 intravenously. The dose of radiation delivered will be 45 Gy in 1.8 Gy fractions for 5 weeks.
Study Type
INTERVENTIONAL
Purpose
TREATMENT
UCSD Cancer Center
La Jolla, California, United States
University of California, Irvine
Orange, California, United States
Palo Alto VA Health Care Systems
Palo Alto, California, United States
The University of Chicago Medical Center
Chicago, Illinois, United States
Johns Hopkins School of Medicine
Baltimore, Maryland, United States
St. Louis University
St Louis, Missouri, United States
University Hospitals of Cleveland
Cleveland, Ohio, United States
US Oncology, Mary Crowley Center
Dallas, Texas, United States
University of Texas/MD Anderson
Houston, Texas, United States
Scott & White Center for Cancer Prevention and Care
Temple, Texas, United States
...and 2 more locations
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