Esophageal Cancer Clinical Trial

Study of TNFeradeâ„¢ Gene Therapy, Radiation, 5-FU and Cisplatin in Esophageal Cancer

Summary

The primary purpose of this study is to assess the safety and feasibility of giving TNFeradeâ„¢ with 5-FU, Cisplatin and radiation therapy to patients with locally advanced, esophageal cancer prior to surgical resection. TNFeradeâ„¢ 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. TNFeradeâ„¢ is a novel way of selective delivery of TNF-alpha to tumor cells.

TNFeradeâ„¢ 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.

View Eligibility Criteria

Eligibility Criteria

Inclusion criteria:

18-75 years for age;
Patients with biopsy proven locally advanced adenocarcinoma or squamous cell carcinoma of the esophagus, stage II, III, who have not received previous treatment and are considered to have resectable carcinoma;
Informed consent;
Karnofsky performance status ≥ 70%;
Life expectancy greater than 6 months.

Exclusion criteria:

Diagnosis of lymphoma of the esophagus;
History of other malignancy in the past 2 years except carcinoma in situ of the cervix or bladder, non-melanomatous skin cancer or localized early stage prostate cancer with patients continuously disease-free;
Previous chemotherapy or radiation for esophageal cancer or previous radiation therapy to the target field;
T4 disease, metastatic (stage IV) disease or confirmed invasion of the bronchial tree;
Extension beyond 2 cm into stomach;
Liver enzymes >2.0 x ULN (ALT, AST, bilirubin, alkaline phosphatase);
Coagulopathy (INR >1.5, PTT ratio >1.5);
Renal insufficiency (creatinine >2.0 mg/dL; calculated creatinine clearance <50 ml/min);
Significant anemia (hematocrit <28% or hemoglobin <9 g/dL) (may have RBC transfusion), or thrombocytopenia (platelet count <100,000/μL)l or leukopenia (WBC <3,000/µL; ANC <1,500 μL);
Contraindication to endoscopic or EUS-guided delivery including obstructive lesions that can not be dilated to pass endoscope;
Clinical evidence of active infection of any type, including hepatitis B or C virus;
Due to the embryotoxic effects of chemotherapy, pregnant or lactating women, or men unable or unwilling to practice contraception are excluded;
Experimental medications within the last four weeks prior to Day 1;
Chronic systemic corticosteriod use (orally or parenterally administered);
Significant concurrent medical or psychiatric illness as defined by the investigator.

Study is for people with:

Esophageal Cancer

Phase:

Phase 2

Study ID:

NCT00051480

Recruitment Status:

Completed

Sponsor:

GenVec

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There are 12 Locations for this study

See Locations Near You

UCSD Cancer Center
La Jolla California, 92093, United States
University of California, Irvine
Orange California, 92868, United States
Palo Alto VA Health Care Systems
Palo Alto California, 94304, United States
The University of Chicago Medical Center
Chicago Illinois, 60637, United States
Johns Hopkins School of Medicine
Baltimore Maryland, 21231, United States
St. Louis University
St. Louis Missouri, 63110, United States
University Hospitals of Cleveland
Cleveland Ohio, 44106, United States
US Oncology, Mary Crowley Center
Dallas Texas, 75246, United States
University of Texas/MD Anderson
Houston Texas, 77030, United States
Scott & White Center for Cancer Prevention and Care
Temple Texas, 76508, United States
Tyler Cancer Center
Tyler Texas, 75702, United States
Medical College of Virginia
Richmond Virginia, 23298, United States

How clear is this clinincal trial information?

Study is for people with:

Esophageal Cancer

Phase:

Phase 2

Study ID:

NCT00051480

Recruitment Status:

Completed

Sponsor:


GenVec

How clear is this clinincal trial information?

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