TNFerade Biologic, an Adenovector With a Radiation-Inducible Promoter, Carrying the Human Tumor Necrosis Factor Alpha Gene: A Phase I Study in Patients With Solid Tumors

Author:

Senzer Neil1,Mani Sridhar1,Rosemurgy Alexander1,Nemunaitis John1,Cunningham Casey1,Guha Chandan1,Bayol Natalia1,Gillen Michelle1,Chu Karen1,Rasmussen Camilla1,Rasmussen Henrik1,Kufe Donald1,Weichselbaum Ralph1,Hanna Nader1

Affiliation:

1. From US Oncology, Dallas, TX; Albert Einstein College of Medicine, Bronx, NY; University of South Florida, Tampa, FL; GenVec Inc, Gaithersburg, MD; Department of Medicine, Dana-Farber Cancer Institute, Boston, MA; University of Chicago Medical Center, Chicago, IL; and the Department of General Surgery, University of Kentucky Medical Center, Lexington, KY

Abstract

PurposeTNFerade is a replication deficient adenovector that expresses human tumor necrosis factor alpha under control of the radiation-inducible Egr-1 promoter. The goals of this study were to determine the safety and toxicity of TNFerade in combination with radiation therapy.Patients and MethodsTNFerade was administered by intratumoral administration, weekly for 6 weeks with concomitant radiation (30 to 70 Gy). Seven dose levels were studied (4 × 107particle units [pu] to 4 × 1011pu) in patients with solid tumors being treated with radiation.ResultsThirty-six patients were assessable for toxicity and 30 for tumor response. Most frequent TNFerade-related toxicities were fever (22%), injection site pain (19%), and chills (19%). No dose-limiting toxicities were observed. Overall, 21 of 30 patients (70%) demonstrated objective tumor response (five complete responses, nine partial responses, and seven minimal responses). In four of five patients with synchronous lesions, a differential response between lesions treated with TNFerade + radiation compared with radiation only was observed.ConclusionThis is the first human study with TNFerade and radiation. The integrated treatment was well tolerated in patients with predominantly prior treatment-refractory solid tumors. Controlled prospective clinical trials have been initiated to more fully define the therapeutic contribution of TNFerade.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

Reference46 articles.

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